Item | Value |
---|---|
geneid | 9388 |
ensemblid | ENSG00000101670.12 |
hgncid | 6623 |
symbol | LIPG |
name | lipase G, endothelial type |
refseq_nuc | NM_006033.4 |
refseq_prot | NP_006024.1 |
ensembl_nuc | ENST00000261292.9 |
ensembl_prot | ENSP00000261292.4 |
mane_status | MANE Select |
chr | chr18 |
start | 49562057 |
end | 49599185 |
strand | + |
ver | v1.2 |
region | chr18:49562057-49599185 |
region5000 | chr18:49557057-49604185 |
regionname0 | LIPG_chr18_49562057_49599185 |
regionname5000 | LIPG_chr18_49557057_49604185 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 500 | 282 | 70 | 64 | 104 | 10 | 33 | 80 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002 | 0/1 | 500 | 85 | 10 | 15 | 45 | 3 | 11 | 32 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0003 | 0/0 | 500 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0004 | 0/0 | 500 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0005 | 0/0 | 500 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0006 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0007 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0008 | 0/0 | 500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1503 | 264 | 54 | 62 | 104 | 10 | 33 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0002 | 0/1 | 1503 | 83 | 10 | 15 | 44 | 3 | 10 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0003 | 0/0 | 1503 | 11 | 10 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0004 | 0/0 | 1503 | 8 | 8 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0005 | 0/0 | 1503 | 6 | 5 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0006 | 0/0 | 1503 | 5 | 5 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0007 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0008 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0009 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0010 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0011 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0012 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
c0013 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8917 | 37 | 6 | 6 | 19 | 2 | 4 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0002 | 0/0 | 8917 | 30 | 0 | 2 | 22 | 0 | 6 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0003 | 0/0 | 8916 | 25 | 7 | 3 | 11 | 0 | 4 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0004 | 0/0 | 8918 | 17 | 0 | 0 | 17 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0005 | 0/0 | 8917 | 15 | 1 | 6 | 4 | 1 | 3 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0006 | 0/0 | 8916 | 11 | 0 | 4 | 5 | 1 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0007 | 0/0 | 8917 | 10 | 9 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0008 | 0/0 | 8917 | 10 | 0 | 7 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0009 | 0/0 | 8917 | 9 | 1 | 2 | 4 | 2 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0010 | 0/0 | 8916 | 8 | 0 | 2 | 0 | 2 | 4 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0011 | 0/0 | 8917 | 8 | 0 | 7 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0012 | 1/0 | 8916 | 8 | 0 | 2 | 0 | 2 | 3 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0013 | 0/0 | 8916 | 7 | 0 | 3 | 4 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0014 | 0/0 | 8918 | 6 | 6 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0015 | 0/0 | 8917 | 6 | 0 | 6 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0016 | 0/0 | 8910 | 5 | 5 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0017 | 0/0 | 8915 | 4 | 4 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0018 | 0/0 | 8918 | 4 | 0 | 0 | 3 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0019 | 0/0 | 8918 | 4 | 0 | 0 | 3 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0020 | 0/0 | 8916 | 3 | 0 | 1 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0021 | 0/0 | 8917 | 3 | 0 | 2 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0022 | 0/0 | 8918 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0023 | 0/0 | 8919 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0024 | 0/0 | 8915 | 3 | 3 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0025 | 0/0 | 8917 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0026 | 0/0 | 8918 | 3 | 3 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0027 | 0/0 | 8916 | 3 | 0 | 1 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0028 | 0/0 | 8918 | 2 | 0 | 1 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0029 | 0/0 | 8917 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0030 | 0/0 | 8919 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0031 | 0/0 | 8917 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0032 | 0/0 | 8916 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0033 | 0/0 | 8915 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0034 | 0/0 | 8916 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0035 | 0/0 | 8917 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0036 | 0/0 | 8916 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0037 | 0/0 | 8918 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0038 | 0/0 | 8927 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0039 | 0/0 | 8915 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0040 | 0/0 | 8915 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0041 | 0/0 | 8918 | 2 | 1 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0042 | 0/0 | 8917 | 2 | 0 | 0 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0043 | 0/0 | 8917 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0044 | 0/0 | 8917 | 2 | 1 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0045 | 0/0 | 8918 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0046 | 0/0 | 8917 | 2 | 0 | 1 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0047 | 0/0 | 8916 | 2 | 0 | 0 | 1 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0048 | 0/0 | 8919 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0049 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0050 | 0/0 | 8919 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0051 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0052 | 0/0 | 8917 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0053 | 0/0 | 8916 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0054 | 0/0 | 8917 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0055 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0056 | 0/0 | 8916 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0057 | 0/0 | 8917 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0058 | 0/0 | 8916 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0059 | 0/0 | 8917 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0060 | 0/0 | 8918 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0061 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0062 | 0/0 | 8919 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0063 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0064 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0065 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0066 | 0/0 | 8919 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0067 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0068 | 0/0 | 8918 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0069 | 0/0 | 8920 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0070 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0071 | 0/0 | 8905 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0072 | 0/0 | 8918 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0073 | 0/0 | 8918 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0074 | 0/1 | 8918 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0075 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0076 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0077 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0078 | 0/0 | 8914 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0079 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0080 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0081 | 0/0 | 8919 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0082 | 0/0 | 8918 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0083 | 0/0 | 8915 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0084 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0085 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0086 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0087 | 0/0 | 8918 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0088 | 0/0 | 8919 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0089 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0090 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0091 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0092 | 0/0 | 8918 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0093 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0094 | 0/0 | 8926 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0095 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0096 | 0/0 | 8928 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0097 | 0/0 | 8915 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0098 | 0/0 | 8925 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0099 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0100 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0101 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0102 | 0/0 | 8915 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0103 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0104 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0105 | 0/0 | 8915 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0106 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0107 | 0/0 | 8918 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0108 | 0/0 | 8915 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0109 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0110 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0111 | 0/0 | 8915 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0112 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0113 | 0/0 | 8916 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0114 | 0/0 | 8916 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0115 | 0/0 | 8915 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0116 | 0/0 | 8915 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0117 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0118 | 0/0 | 8918 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0119 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0120 | 0/0 | 8918 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0121 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0122 | 0/0 | 8916 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0123 | 0/0 | 8917 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0124 | 0/0 | 8917 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0125 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0126 | 0/0 | 8918 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0127 | 0/0 | 8918 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0128 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0129 | 0/0 | 8916 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0130 | 0/0 | 8919 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0131 | 0/0 | 8917 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0132 | 0/0 | 8917 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0133 | 0/0 | 8916 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0134 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0135 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0136 | 0/0 | 8917 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0137 | 0/0 | 8917 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0138 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0139 | 0/0 | 8935 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0140 | 0/0 | 8918 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0141 | 0/0 | 8931 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0142 | 0/0 | 8917 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
t0143 | 0/0 | 8919 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0373 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1503 | 264 | 54 | 62 | 104 | 10 | 33 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0001c0003 | 0/0 | 1503 | 11 | 10 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0001c0005 | 0/0 | 1503 | 6 | 5 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0001c0011 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0002c0002 | 0/1 | 1503 | 83 | 10 | 15 | 44 | 3 | 10 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0002c0012 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0002c0013 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0003c0004 | 0/0 | 1503 | 8 | 8 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0004c0006 | 0/0 | 1503 | 5 | 5 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0005c0010 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0006c0008 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0007c0007 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 | |
a0008c0009 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10419 | 37 | 6 | 6 | 19 | 2 | 4 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0002 | 0/0 | 10419 | 30 | 0 | 2 | 22 | 0 | 6 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0003 | 0/0 | 10418 | 25 | 7 | 3 | 11 | 0 | 4 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0006 | 0/0 | 10418 | 11 | 0 | 4 | 5 | 1 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0008 | 0/0 | 10419 | 9 | 0 | 7 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0010 | 0/0 | 10418 | 7 | 0 | 2 | 0 | 1 | 4 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0011 | 0/0 | 10419 | 8 | 0 | 7 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0012 | 1/0 | 10418 | 8 | 0 | 2 | 0 | 2 | 3 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0013 | 0/0 | 10418 | 6 | 0 | 2 | 4 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0015 | 0/0 | 10419 | 6 | 0 | 6 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0017 | 0/0 | 10417 | 4 | 4 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0018 | 0/0 | 10420 | 3 | 0 | 0 | 2 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0019 | 0/0 | 10420 | 4 | 0 | 0 | 3 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0020 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0024 | 0/0 | 10417 | 3 | 3 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0025 | 0/0 | 10419 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0026 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0027 | 0/0 | 10418 | 3 | 0 | 1 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0032 | 0/0 | 10418 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0033 | 0/0 | 10417 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0034 | 0/0 | 10418 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0035 | 0/0 | 10419 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0036 | 0/0 | 10418 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0037 | 0/0 | 10420 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0038 | 0/0 | 10429 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0039 | 0/0 | 10417 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0040 | 0/0 | 10417 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0041 | 0/0 | 10420 | 2 | 1 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0042 | 0/0 | 10419 | 2 | 0 | 0 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0043 | 0/0 | 10419 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0044 | 0/0 | 10419 | 2 | 1 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0046 | 0/0 | 10419 | 2 | 0 | 1 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0047 | 0/0 | 10418 | 2 | 0 | 0 | 1 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0048 | 0/0 | 10421 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0049 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0052 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0053 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0055 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0056 | 0/0 | 10418 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0061 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0076 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0077 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0078 | 0/0 | 10416 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0079 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0081 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0082 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0083 | 0/0 | 10417 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0084 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0085 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0086 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0089 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0090 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0091 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0092 | 0/0 | 10420 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0093 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0094 | 0/0 | 10428 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0095 | 0/0 | 10430 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0096 | 0/0 | 10430 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0097 | 0/0 | 10417 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0098 | 0/0 | 10427 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0101 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0102 | 0/0 | 10417 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0104 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0105 | 0/0 | 10417 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0106 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0107 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0108 | 0/0 | 10417 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0110 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0111 | 0/0 | 10417 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0112 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0113 | 0/0 | 10418 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0114 | 0/0 | 10418 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0115 | 0/0 | 10417 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0116 | 0/0 | 10417 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0117 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0119 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0120 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0122 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0123 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0124 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0125 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0126 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0127 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0128 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0129 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0131 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0132 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0133 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0134 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0135 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0136 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0137 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0138 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0139 | 0/0 | 10437 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0140 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0141 | 0/0 | 10433 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0142 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0001t0143 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0003t0007 | 0/0 | 10419 | 6 | 5 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0003t0045 | 0/0 | 10420 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0003t0099 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0003t0118 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0003t0121 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0005t0007 | 0/0 | 10419 | 4 | 4 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0005t0100 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0005t0103 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0001c0011t0068 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0004 | 0/0 | 10420 | 16 | 0 | 0 | 16 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0005 | 0/0 | 10419 | 15 | 1 | 6 | 4 | 1 | 3 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0009 | 0/0 | 10419 | 9 | 1 | 2 | 4 | 2 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0014 | 0/0 | 10420 | 6 | 6 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0018 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0020 | 0/0 | 10418 | 2 | 0 | 0 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0021 | 0/0 | 10419 | 3 | 0 | 2 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0022 | 0/0 | 10420 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0023 | 0/0 | 10421 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0028 | 0/0 | 10420 | 2 | 0 | 1 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0030 | 0/0 | 10421 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0031 | 0/0 | 10419 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0050 | 0/0 | 10421 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0051 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0054 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0058 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0059 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0060 | 0/0 | 10420 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0062 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0063 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0064 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0065 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0066 | 0/0 | 10421 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0067 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0069 | 0/0 | 10422 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0070 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0071 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0072 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0073 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0074 | 0/1 | 10420 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0002t0130 | 0/0 | 10421 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0012t0057 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0002c0013t0004 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0003c0004t0016 | 0/0 | 10412 | 5 | 5 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0003c0004t0026 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0003c0004t0080 | 0/0 | 10412 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0003c0004t0109 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0004c0006t0029 | 0/0 | 10419 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0004c0006t0075 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0004c0006t0087 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0004c0006t0088 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0005c0010t0010 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0006c0008t0008 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0007c0007t0026 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
a0008c0009t0013 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | copy fasta | chr18 | 49557057 | 49604185 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0013g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0013g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0015g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0015g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0015g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0015g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0015g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0017g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0017g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0017g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0017g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0018g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0018g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0018g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0019g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0019g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0019g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0019g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0020g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0024g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0024g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0024g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0025g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0025g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0025g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0026g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0027g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0027g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0027g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0032g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0032g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0033g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0033g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0034g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0034g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0035g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0035g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0036g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0036g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0037g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0037g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0038g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0038g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0039g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0039g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0040g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0040g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0041g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0041g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0042g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0042g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0043g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0043g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0044g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0044g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0046g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0046g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0047g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0047g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0048g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0049g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0052g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0053g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0055g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0056g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0061g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0076g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0077g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0078g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0079g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0081g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0082g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0083g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0084g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0085g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0086g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0089g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0090g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0091g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0092g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0093g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0094g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0095g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0096g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0097g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0098g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0101g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0102g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0104g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0105g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0106g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0107g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0108g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0110g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0111g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0112g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0113g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0114g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0115g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0116g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0117g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0119g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0120g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0122g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0123g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0124g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0125g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0126g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0127g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0128g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0129g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0131g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0132g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0133g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0134g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0135g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0136g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0137g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0138g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0139g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0140g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0141g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0142g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0001t0143g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0045g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0045g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0099g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0118g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0003t0121g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0005t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0005t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0005t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0005t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0005t0100g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0005t0103g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0001c0011t0068g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0005g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0009g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0014g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0014g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0014g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0014g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0014g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0014g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0018g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0020g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0020g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0021g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0021g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0021g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0022g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0022g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0022g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0023g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0023g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0023g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0028g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0028g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0030g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0030g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0031g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0031g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0050g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0051g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0054g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0058g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0059g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0060g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0062g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0063g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0064g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0065g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0066g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0067g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0069g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0070g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0071g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0072g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0073g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0074g0373 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0002t0130g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0012t0057g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0002c0013t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0016g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0016g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0026g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0080g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0003c0004t0109g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0004c0006t0029g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0004c0006t0029g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0004c0006t0075g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0004c0006t0087g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0004c0006t0088g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0005c0010t0010g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0006c0008t0008g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0007c0007t0026g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
a0008c0009t0013g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0046 | g0086 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0042 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00140 | hp1 | a0002 | c0002 | t0009 | g0361 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0069 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00280 | hp2 | a0002 | c0002 | t0009 | g0356 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00323 | hp2 | a0001 | c0001 | t0131 | g0279 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00423 | hp1 | a0001 | c0001 | t0119 | g0294 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00423 | hp2 | a0002 | c0002 | t0009 | g0291 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00438 | hp1 | a0001 | c0001 | t0044 | g0238 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00438 | hp2 | a0001 | c0001 | t0140 | g0104 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00544 | hp2 | a0001 | c0001 | t0008 | g0293 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0078 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00558 | hp2 | a0002 | c0002 | t0004 | g0312 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00609 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00609 | hp2 | a0002 | c0002 | t0004 | g0311 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0087 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0152 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00642 | hp1 | a0001 | c0001 | t0015 | g0028 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00642 | hp2 | a0002 | c0002 | t0028 | g0354 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00733 | hp1 | a0001 | c0001 | t0020 | g0375 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00735 | hp1 | a0001 | c0001 | t0142 | g0159 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00738 | hp1 | a0001 | c0001 | t0083 | g0274 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00741 | hp1 | a0001 | c0001 | t0052 | g0374 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0067 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01069 | hp1 | a0001 | c0001 | t0136 | g0281 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01070 | hp2 | a0002 | c0002 | t0005 | g0365 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01071 | hp1 | a0002 | c0002 | t0005 | g0346 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01074 | hp2 | a0001 | c0001 | t0015 | g0001 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0023 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01081 | hp2 | a0001 | c0001 | t0112 | g0020 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01099 | hp1 | a0002 | c0002 | t0005 | g0366 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01106 | hp2 | a0002 | c0002 | t0009 | g0357 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0006 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01109 | hp2 | a0001 | c0003 | t0007 | g0200 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01167 | hp1 | a0002 | c0002 | t0021 | g0378 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0001 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01168 | hp1 | a0001 | c0001 | t0012 | g0123 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01175 | hp1 | a0001 | c0001 | t0046 | g0096 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01175 | hp2 | a0002 | c0002 | t0072 | g0363 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01192 | hp1 | a0001 | c0001 | t0011 | g0005 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01192 | hp2 | a0001 | c0001 | t0015 | g0024 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01243 | hp2 | a0001 | c0001 | t0048 | g0271 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01256 | hp1 | a0002 | c0002 | t0005 | g0367 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01256 | hp2 | a0002 | c0002 | t0051 | g0342 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01257 | hp1 | a0001 | c0001 | t0090 | g0109 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01257 | hp2 | a0001 | c0001 | t0102 | g0143 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01258 | hp1 | a0002 | c0002 | t0005 | g0341 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01258 | hp2 | a0001 | c0001 | t0106 | g0144 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01261 | hp1 | a0001 | c0001 | t0008 | g0203 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01261 | hp2 | a0001 | c0001 | t0034 | g0101 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01346 | hp1 | a0001 | c0001 | t0128 | g0040 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01346 | hp2 | a0002 | c0002 | t0021 | g0377 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01358 | hp1 | a0001 | c0005 | t0100 | g0183 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01358 | hp2 | a0001 | c0001 | t0041 | g0004 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01361 | hp1 | a0001 | c0001 | t0127 | g0050 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01361 | hp2 | a0002 | c0002 | t0073 | g0372 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01433 | hp1 | a0001 | c0001 | t0011 | g0065 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01433 | hp2 | a0001 | c0001 | t0013 | g0084 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01496 | hp1 | a0001 | c0001 | t0011 | g0062 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01516 | hp1 | a0001 | c0001 | t0010 | g0149 | EUR | IBS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01516 | hp2 | a0001 | c0001 | t0019 | g0249 | EUR | IBS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01884 | hp1 | a0001 | c0001 | t0026 | g0270 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01884 | hp2 | a0001 | c0005 | t0007 | g0177 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01891 | hp1 | a0001 | c0001 | t0044 | g0035 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01891 | hp2 | a0001 | c0001 | t0032 | g0022 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0192 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01928 | hp2 | a0001 | c0001 | t0027 | g0205 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01934 | hp1 | a0001 | c0001 | t0008 | g0193 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01943 | hp1 | a0001 | c0001 | t0010 | g0150 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01943 | hp2 | a0001 | c0001 | t0011 | g0064 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01975 | hp1 | a0001 | c0001 | t0129 | g0138 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0184 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01978 | hp1 | a0001 | c0001 | t0013 | g0099 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01978 | hp2 | a0001 | c0001 | t0126 | g0063 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01981 | hp1 | a0001 | c0001 | t0015 | g0027 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01981 | hp2 | a0001 | c0001 | t0035 | g0113 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01993 | hp1 | a0002 | c0002 | t0059 | g0352 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02004 | hp1 | a0001 | c0001 | t0035 | g0116 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02015 | hp1 | a0002 | c0002 | t0004 | g0302 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02015 | hp2 | a0002 | c0002 | t0064 | g0379 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02040 | hp1 | a0001 | c0001 | t0040 | g0053 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0079 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02055 | hp1 | a0001 | c0001 | t0032 | g0021 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02055 | hp2 | a0003 | c0004 | t0016 | g0148 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02056 | hp2 | a0002 | c0002 | t0005 | g0353 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02071 | hp1 | a0001 | c0001 | t0038 | g0025 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02074 | hp1 | a0001 | c0001 | t0025 | g0085 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02074 | hp2 | a0002 | c0002 | t0023 | g0313 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02080 | hp1 | a0001 | c0001 | t0125 | g0060 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02083 | hp1 | a0001 | c0001 | t0093 | g0075 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02083 | hp2 | a0002 | c0002 | t0063 | g0304 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02129 | hp1 | a0002 | c0002 | t0004 | g0300 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02129 | hp2 | a0001 | c0001 | t0013 | g0102 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02132 | hp1 | a0002 | c0002 | t0004 | g0316 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02145 | hp1 | a0001 | c0001 | t0120 | g0174 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02145 | hp2 | a0001 | c0001 | t0033 | g0275 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02148 | hp1 | a0001 | c0001 | t0008 | g0197 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02148 | hp2 | a0001 | c0001 | t0034 | g0090 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02155 | hp1 | a0002 | c0002 | t0065 | g0369 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02155 | hp2 | a0002 | c0002 | t0022 | g0305 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02257 | hp1 | a0002 | c0002 | t0009 | g0351 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02257 | hp2 | a0001 | c0001 | t0107 | g0190 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02258 | hp1 | a0001 | c0005 | t0007 | g0179 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02258 | hp2 | a0001 | c0001 | t0039 | g0178 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02280 | hp2 | a0002 | c0002 | t0005 | g0340 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02293 | hp1 | a0001 | c0001 | t0011 | g0066 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02293 | hp2 | a0008 | c0009 | t0013 | g0120 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02451 | hp2 | a0001 | c0001 | t0039 | g0189 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02523 | hp2 | a0006 | c0008 | t0008 | g0295 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02572 | hp1 | a0001 | c0001 | t0143 | g0239 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02572 | hp2 | a0001 | c0001 | t0017 | g0288 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02602 | hp1 | a0001 | c0001 | t0139 | g0230 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02602 | hp2 | a0002 | c0012 | t0057 | g0368 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02615 | hp1 | a0002 | c0002 | t0014 | g0333 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02615 | hp2 | a0001 | c0003 | t0045 | g0202 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02622 | hp2 | a0001 | c0001 | t0094 | g0030 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02630 | hp1 | a0001 | c0001 | t0017 | g0287 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02630 | hp2 | a0001 | c0003 | t0007 | g0195 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02647 | hp1 | a0001 | c0001 | t0104 | g0163 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02647 | hp2 | a0004 | c0006 | t0075 | g0264 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02717 | hp2 | a0001 | c0001 | t0033 | g0276 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02723 | hp1 | a0001 | c0001 | t0076 | g0049 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02723 | hp2 | a0002 | c0002 | t0014 | g0334 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02735 | hp1 | a0001 | c0001 | t0108 | g0153 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02735 | hp2 | a0001 | c0001 | t0115 | g0045 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02809 | hp1 | a0001 | c0001 | t0024 | g0046 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02809 | hp2 | a0001 | c0001 | t0017 | g0285 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02818 | hp1 | a0001 | c0001 | t0017 | g0290 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02818 | hp2 | a0001 | c0001 | t0141 | g0250 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02886 | hp1 | a0003 | c0004 | t0026 | g0168 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02886 | hp2 | a0001 | c0003 | t0099 | g0198 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02895 | hp1 | a0001 | c0001 | t0078 | g0286 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02896 | hp1 | a0001 | c0001 | t0122 | g0185 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02896 | hp2 | a0001 | c0001 | t0105 | g0162 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02922 | hp1 | a0001 | c0001 | t0024 | g0048 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02922 | hp2 | a0001 | c0005 | t0007 | g0180 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02965 | hp1 | a0001 | c0001 | t0096 | g0029 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02970 | hp1 | a0001 | c0001 | t0110 | g0164 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02970 | hp2 | a0001 | c0003 | t0007 | g0194 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02976 | hp1 | a0004 | c0006 | t0087 | g0170 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02976 | hp2 | a0003 | c0004 | t0016 | g0166 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0165 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03041 | hp1 | a0001 | c0001 | t0082 | g0272 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03041 | hp2 | a0001 | c0005 | t0103 | g0176 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03098 | hp1 | a0004 | c0006 | t0029 | g0265 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03098 | hp2 | a0001 | c0003 | t0045 | g0201 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03130 | hp1 | a0001 | c0005 | t0007 | g0182 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03130 | hp2 | a0003 | c0004 | t0080 | g0147 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03139 | hp1 | a0001 | c0003 | t0121 | g0181 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03139 | hp2 | a0002 | c0002 | t0014 | g0336 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03195 | hp1 | a0002 | c0002 | t0070 | g0345 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03195 | hp2 | a0001 | c0001 | t0079 | g0289 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03209 | hp1 | a0001 | c0003 | t0007 | g0188 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03225 | hp1 | a0002 | c0002 | t0014 | g0332 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03225 | hp2 | a0001 | c0001 | t0077 | g0031 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03239 | hp1 | a0002 | c0002 | t0054 | g0344 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03239 | hp2 | a0001 | c0001 | t0012 | g0072 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03453 | hp1 | a0001 | c0003 | t0007 | g0199 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03453 | hp2 | a0001 | c0001 | t0085 | g0263 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03486 | hp1 | a0002 | c0002 | t0062 | g0381 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03486 | hp2 | a0001 | c0003 | t0118 | g0186 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03491 | hp1 | a0002 | c0002 | t0058 | g0308 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03516 | hp1 | a0001 | c0001 | t0081 | g0269 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03579 | hp1 | a0001 | c0001 | t0117 | g0161 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03579 | hp2 | a0001 | c0001 | t0084 | g0258 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03654 | hp1 | a0001 | c0001 | t0010 | g0158 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03654 | hp2 | a0001 | c0001 | t0012 | g0142 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03669 | hp2 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0155 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03704 | hp1 | a0001 | c0001 | t0132 | g0234 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03710 | hp1 | a0002 | c0002 | t0020 | g0309 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03831 | hp1 | a0001 | c0001 | t0124 | g0154 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03834 | hp1 | a0001 | c0001 | t0047 | g0207 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0008 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03927 | hp1 | a0002 | c0002 | t0060 | g0359 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03942 | hp1 | a0001 | c0001 | t0053 | g0338 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03942 | hp2 | a0002 | c0002 | t0020 | g0310 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04115 | hp1 | a0001 | c0001 | t0092 | g0257 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04115 | hp2 | a0002 | c0002 | t0005 | g0364 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04184 | hp1 | a0002 | c0002 | t0028 | g0343 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04184 | hp2 | a0001 | c0001 | t0018 | g0141 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04199 | hp1 | a0001 | c0001 | t0042 | g0157 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04199 | hp2 | a0001 | c0001 | t0042 | g0156 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04204 | hp1 | a0002 | c0002 | t0021 | g0376 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04204 | hp2 | a0001 | c0001 | t0010 | g0151 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0088 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG04228 | hp2 | a0002 | c0002 | t0005 | g0348 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18612 | hp1 | a0002 | c0002 | t0005 | g0003 | EAS | CHB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18612 | hp2 | a0001 | c0001 | t0137 | g0100 | EAS | CHB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18906 | hp1 | a0003 | c0004 | t0016 | g0146 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18939 | hp1 | a0002 | c0002 | t0004 | g0319 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18939 | hp2 | a0002 | c0002 | t0009 | g0355 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18941 | hp1 | a0001 | c0001 | t0019 | g0231 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18944 | hp1 | a0001 | c0001 | t0089 | g0253 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18944 | hp2 | a0001 | c0001 | t0098 | g0268 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18947 | hp1 | a0002 | c0002 | t0009 | g0358 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18947 | hp2 | a0001 | c0001 | t0138 | g0221 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18948 | hp2 | a0001 | c0001 | t0027 | g0240 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18954 | hp2 | a0001 | c0001 | t0043 | g0252 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18956 | hp2 | a0002 | c0002 | t0004 | g0297 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18962 | hp1 | a0002 | c0013 | t0004 | g0328 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18964 | hp1 | a0002 | c0002 | t0022 | g0317 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18966 | hp2 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18970 | hp1 | a0001 | c0001 | t0091 | g0076 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18970 | hp2 | a0002 | c0002 | t0004 | g0299 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18971 | hp1 | a0001 | c0001 | t0018 | g0130 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18974 | hp1 | a0002 | c0002 | t0023 | g0307 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18977 | hp1 | a0001 | c0001 | t0011 | g0277 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18981 | hp1 | a0002 | c0002 | t0004 | g0314 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18981 | hp2 | a0001 | c0001 | t0056 | g0296 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18982 | hp1 | a0001 | c0001 | t0013 | g0106 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18982 | hp2 | a0001 | c0001 | t0036 | g0259 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18983 | hp1 | a0002 | c0002 | t0004 | g0298 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18983 | hp2 | a0002 | c0002 | t0004 | g0370 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18985 | hp1 | a0001 | c0001 | t0025 | g0254 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18991 | hp1 | a0001 | c0001 | t0040 | g0112 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18991 | hp2 | a0002 | c0002 | t0066 | g0303 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18998 | hp1 | a0002 | c0002 | t0009 | g0347 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18998 | hp2 | a0002 | c0002 | t0030 | g0315 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18999 | hp2 | a0001 | c0001 | t0116 | g0124 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19004 | hp1 | a0001 | c0001 | t0019 | g0219 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19005 | hp1 | a0002 | c0002 | t0004 | g0301 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19010 | hp1 | a0002 | c0002 | t0031 | g0324 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19011 | hp1 | a0001 | c0001 | t0019 | g0248 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19011 | hp2 | a0002 | c0002 | t0005 | g0350 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19012 | hp1 | a0001 | c0001 | t0101 | g0191 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19012 | hp2 | a0001 | c0001 | t0038 | g0172 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19030 | hp1 | a0001 | c0001 | t0049 | g0292 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19030 | hp2 | a0004 | c0006 | t0029 | g0266 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19043 | hp1 | a0001 | c0001 | t0061 | g0036 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19055 | hp1 | a0002 | c0002 | t0004 | g0330 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19055 | hp2 | a0001 | c0001 | t0111 | g0098 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19056 | hp2 | a0002 | c0002 | t0022 | g0321 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19057 | hp1 | a0002 | c0002 | t0004 | g0320 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19057 | hp2 | a0002 | c0002 | t0030 | g0322 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19058 | hp1 | a0001 | c0001 | t0097 | g0267 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19058 | hp2 | a0001 | c0001 | t0027 | g0216 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19060 | hp1 | a0002 | c0002 | t0067 | g0327 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19063 | hp1 | a0001 | c0001 | t0025 | g0132 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19063 | hp2 | a0002 | c0002 | t0069 | g0331 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19064 | hp1 | a0002 | c0002 | t0031 | g0325 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19064 | hp2 | a0002 | c0002 | t0004 | g0306 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19067 | hp1 | a0002 | c0002 | t0130 | g0171 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19070 | hp1 | a0001 | c0001 | t0113 | g0082 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19074 | hp1 | a0001 | c0001 | t0047 | g0242 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19074 | hp2 | a0001 | c0001 | t0036 | g0133 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19079 | hp1 | a0002 | c0002 | t0023 | g0329 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19079 | hp2 | a0001 | c0001 | t0134 | g0217 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19080 | hp1 | a0002 | c0002 | t0005 | g0349 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19081 | hp1 | a0001 | c0001 | t0135 | g0220 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19081 | hp2 | a0001 | c0001 | t0037 | g0077 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19082 | hp1 | a0001 | c0001 | t0043 | g0114 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19083 | hp1 | a0002 | c0002 | t0050 | g0323 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19084 | hp1 | a0002 | c0002 | t0071 | g0362 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19087 | hp2 | a0002 | c0002 | t0004 | g0318 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19088 | hp1 | a0002 | c0002 | t0018 | g0173 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19088 | hp2 | a0001 | c0001 | t0114 | g0055 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19089 | hp1 | a0001 | c0001 | t0037 | g0136 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19089 | hp2 | a0001 | c0001 | t0013 | g0057 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19091 | hp1 | a0001 | c0001 | t0018 | g0071 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19240 | hp1 | a0001 | c0001 | t0123 | g0012 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA19240 | hp2 | a0001 | c0001 | t0055 | g0326 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ASW | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20129 | hp2 | a0001 | c0001 | t0041 | g0160 | AFR | ASW | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20752 | hp1 | a0002 | c0002 | t0005 | g0339 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20752 | hp2 | a0005 | c0010 | t0010 | g0255 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20805 | hp1 | a0001 | c0001 | t0133 | g0228 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20805 | hp2 | a0001 | c0001 | t0012 | g0051 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | GIH | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | GIH | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01123 | hp1 | a0002 | c0002 | t0005 | g0371 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG01123 | hp2 | a0002 | c0002 | t0009 | g0360 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02109 | hp1 | a0003 | c0004 | t0016 | g0145 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02109 | hp2 | a0002 | c0002 | t0014 | g0337 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02486 | hp1 | a0001 | c0001 | t0086 | g0273 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02559 | hp1 | a0004 | c0006 | t0088 | g0169 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0047 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03471 | hp1 | a0001 | c0003 | t0007 | g0187 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG03471 | hp2 | a0007 | c0007 | t0026 | g0007 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG06807 | hp1 | a0003 | c0004 | t0109 | g0204 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
HG06807 | hp2 | a0001 | c0011 | t0068 | g0380 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20300 | hp1 | a0003 | c0004 | t0016 | g0167 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA21309 | hp1 | a0002 | c0002 | t0014 | g0335 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
NA21309 | hp2 | a0001 | c0001 | t0095 | g0026 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0074 | g0373 | REF | REF | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0089 | REF | REF | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:49562384 | G | A | 1 | a0003 | 8 | HG02055.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
missense_variant | MODERATE | c.76G>A | p.Gly26Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 328/10418 | 76/1503 | 26/500 | chr18 | 49562384 | ||
chr18:49567494 | C | T | 1 | a0002 | 85 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(82): Show |
missense_variant | MODERATE | c.332C>T | p.Thr111Ile | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/10 | 584/10418 | 332/1503 | 111/500 | chr18 | 49567494 | ||
chr18:49581514 | C | G | 1 | a0004 | 5 | HG02559.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.893C>G | p.Thr298Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1145/10418 | 893/1503 | 298/500 | chr18 | 49581514 | ||
chr18:49581514 | C | T | 1 | a0005 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.893C>T | p.Thr298Ile | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1145/10418 | 893/1503 | 298/500 | chr18 | 49581514 | ||
chr18:49581535 | A | G | 1 | a0008 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.914A>G | p.Lys305Arg | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1166/10418 | 914/1503 | 305/500 | chr18 | 49581535 | ||
chr18:49582407 | T | C | 1 | a0007 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1082T>C | p.Met361Thr | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/10 | 1334/10418 | 1082/1503 | 361/500 | chr18 | 49582407 | ||
chr18:49583689 | C | T | 1 | a0006 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1291C>T | p.Arg431Cys | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/10 | 1543/10418 | 1291/1503 | 431/500 | chr18 | 49583689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:49562320 | C | A | 1 | a0001c0003 | 11 | HG01109.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
synonymous_variant | LOW | c.12C>A | p.Ser4Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 264/10418 | 12/1503 | 4/500 | chr18 | 49562320 | ||
chr18:49562371 | C | T | 2 | a0001c0003a0001c0005 | 17 | HG01109.hp2 HG01358.hp1 HG01884.hp2 others(14): Show |
synonymous_variant | LOW | c.63C>T | p.Ser21Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 315/10418 | 63/1503 | 21/500 | chr18 | 49562371 | ||
chr18:49569487 | C | T | 1 | a0001c0011 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.510C>T | p.Leu170Leu | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/10 | 762/10418 | 510/1503 | 170/500 | chr18 | 49569487 | ||
chr18:49575382 | C | G | 1 | a0002c0013 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.585C>G | p.Ala195Ala | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/10 | 837/10418 | 585/1503 | 195/500 | chr18 | 49575382 | ||
chr18:49581629 | A | T | 1 | a0002c0012 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.1008A>T | p.Leu336Leu | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1260/10418 | 1008/1503 | 336/500 | chr18 | 49581629 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:49562092 | A | G | 1 | a0001c0001t0143 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 217 | chr18 | 49562092 | |||||
chr18:49562285 | T | G | 42 | a0001c0001t0020a0001c0001t0048a0001c0001t0049others(39): Show | 95 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(92): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | chr18 | 49562285 | ||||||
chr18:49590746 | C | T | 1 | a0004c0006t0075 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 224 | chr18 | 49590746 | |||||
chr18:49590764 | G | C | 1 | a0001c0001t0032 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*242G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 242 | chr18 | 49590764 | |||||
chr18:49590804 | T | C | 38 | a0001c0001t0002a0001c0001t0017a0001c0001t0024others(35): Show | 83 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*282T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 282 | chr18 | 49590804 | |||||
chr18:49590837 | A | G | 7 | a0001c0001t0142a0002c0002t0009a0002c0002t0070others(4): Show | 15 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*315A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 315 | chr18 | 49590837 | |||||
chr18:49590868 | G | A | 2 | a0001c0001t0039a0004c0006t0075 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*346G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 346 | chr18 | 49590868 | |||||
chr18:49590883 | C | T | 2 | a0001c0001t0097a0001c0001t0098 | 2 | NA18944.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*361C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 361 | chr18 | 49590883 | |||||
chr18:49590951 | G | A | 2 | a0001c0001t0076a0001c0001t0077 | 2 | HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*429G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 429 | chr18 | 49590951 | |||||
chr18:49590970 | C | T | 7 | a0001c0001t0038a0001c0001t0039a0001c0001t0094others(4): Show | 9 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*448C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 448 | chr18 | 49590970 | |||||
chr18:49591001 | C | T | 4 | a0001c0001t0038a0001c0001t0094a0001c0001t0095others(1): Show | 5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*479C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 479 | chr18 | 49591001 | |||||
chr18:49591004 | A | G | 73 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(70): Show | 189 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 482 | chr18 | 49591004 | |||||
chr18:49591006 | C | T | 12 | a0001c0001t0002a0001c0001t0034a0001c0001t0035others(9): Show | 45 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*484C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 484 | chr18 | 49591006 | |||||
chr18:49591078 | A | G | 11 | a0001c0001t0038a0001c0001t0039a0001c0001t0094others(8): Show | 13 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*556A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 556 | chr18 | 49591078 | |||||
chr18:49591407 | C | T | 2 | a0001c0001t0039a0004c0006t0075 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*885C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 885 | chr18 | 49591407 | |||||
chr18:49591430 | G | A | 2 | a0001c0001t0039a0004c0006t0075 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 908 | chr18 | 49591430 | |||||
chr18:49591539 | A | G | 2 | a0001c0001t0097a0001c0001t0098 | 2 | NA18944.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1017 | chr18 | 49591539 | |||||
chr18:49591543 | C | CATACAGA others(7): Show |
1 | a0001c0001t0141 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1022_*1023insTACA others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1023 | INFO_REALIGN_3_PRIME | chr18 | 49591543 | ||||
chr18:49591564 | C | T | 2 | a0001c0001t0039a0004c0006t0075 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1042C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1042 | chr18 | 49591564 | |||||
chr18:49591582 | G | A | 1 | a0001c0001t0032 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1060G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1060 | chr18 | 49591582 | |||||
chr18:49591609 | T | A | 12 | a0001c0001t0002a0001c0001t0034a0001c0001t0035others(9): Show | 45 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1087T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1087 | chr18 | 49591609 | |||||
chr18:49591729 | C | T | 2 | a0001c0001t0039a0004c0006t0075 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1207C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1207 | chr18 | 49591729 | |||||
chr18:49591800 | A | G | 13 | a0001c0001t0024a0001c0001t0032a0001c0001t0033others(10): Show | 17 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1278A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1278 | chr18 | 49591800 | |||||
chr18:49591805 | A | C | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1283A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1283 | chr18 | 49591805 | |||||
chr18:49591806 | C | A | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1284 | chr18 | 49591806 | |||||
chr18:49591849 | T | C | 12 | a0001c0001t0002a0001c0001t0034a0001c0001t0035others(9): Show | 45 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1327T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1327 | chr18 | 49591849 | |||||
chr18:49591931 | T | C | 1 | a0001c0003t0099 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1409T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1409 | chr18 | 49591931 | |||||
chr18:49591948 | A | G | 1 | a0001c0001t0129 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1426 | chr18 | 49591948 | |||||
chr18:49591978 | CT | C | 4 | a0001c0001t0034a0001c0001t0035a0001c0001t0090others(1): Show | 6 | HG01257.hp1 HG01261.hp2 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1466delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1466 | INFO_REALIGN_3_PRIME | chr18 | 49591978 | ||||
chr18:49591988 | T | A | 1 | a0001c0001t0089 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1466 | chr18 | 49591988 | |||||
chr18:49592028 | T | C | 36 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(33): Show | 98 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1506T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1506 | chr18 | 49592028 | |||||
chr18:49592226 | A | G | 1 | a0001c0001t0061 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1704A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1704 | chr18 | 49592226 | |||||
chr18:49592229 | A | G | 1 | a0001c0001t0086 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1707A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1707 | chr18 | 49592229 | |||||
chr18:49592236 | C | T | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1714C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1714 | chr18 | 49592236 | |||||
chr18:49592237 | T | C | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1715 | chr18 | 49592237 | |||||
chr18:49592388 | A | G | 4 | a0001c0001t0039a0001c0001t0097a0001c0001t0098others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1866A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1866 | chr18 | 49592388 | |||||
chr18:49592485 | C | T | 1 | a0001c0001t0128 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1963C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1963 | chr18 | 49592485 | |||||
chr18:49592521 | T | C | 1 | a0001c0001t0101 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1999 | chr18 | 49592521 | |||||
chr18:49592525 | G | A | 1 | a0002c0002t0062 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2003G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2003 | chr18 | 49592525 | |||||
chr18:49592553 | T | G | 55 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(52): Show | 123 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2031T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2031 | chr18 | 49592553 | |||||
chr18:49592575 | A | AGTTTTGG others(10): Show |
1 | a0001c0001t0139 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054_*2070dupGTTT others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2071 | INFO_REALIGN_3_PRIME | chr18 | 49592575 | ||||
chr18:49592816 | TA | T | 9 | a0001c0001t0038a0001c0001t0039a0001c0001t0094others(6): Show | 11 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2301delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2301 | INFO_REALIGN_3_PRIME | chr18 | 49592816 | ||||
chr18:49592919 | A | G | 1 | a0001c0001t0032 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2397A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2397 | chr18 | 49592919 | |||||
chr18:49592924 | A | AT | 36 | a0001c0001t0002a0001c0001t0019a0001c0001t0025others(33): Show | 82 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2428dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | A | ATT | 18 | a0001c0001t0018a0001c0001t0035a0001c0001t0081others(15): Show | 39 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2427_*2428dupTT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | A | ATTT | 4 | a0001c0001t0048a0002c0002t0023a0002c0002t0066others(1): Show | 6 | HG01243.hp2 HG02074.hp2 NA18974.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2426_*2428dupTTT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0098 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2419_*2428dupTTTT others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0038a0001c0001t0094 | 3 | HG02071.hp1 HG02622.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2418_*2428dupTTTT others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0095 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2417_*2428dupTTTT others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0096 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416_*2428dupTTTT others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592924 | AT | A | 14 | a0001c0001t0017a0001c0001t0024a0001c0001t0027others(11): Show | 23 | HG00323.hp2 HG00738.hp1 HG01256.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2428delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2428 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | ||||
chr18:49592974 | C | T | 17 | a0001c0001t0001a0001c0001t0015a0001c0001t0019others(14): Show | 65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2452C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2452 | chr18 | 49592974 | |||||
chr18:49593004 | C | T | 1 | a0001c0011t0068 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2482C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2482 | chr18 | 49593004 | |||||
chr18:49593053 | T | C | 148 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(145): Show | 372 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(369): Show |
3_prime_UTR_variant | MODIFIER | c.*2531T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2531 | chr18 | 49593053 | |||||
chr18:49593058 | G | A | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2536G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2536 | chr18 | 49593058 | |||||
chr18:49593159 | C | T | 10 | a0001c0001t0024a0001c0001t0032a0001c0001t0033others(7): Show | 14 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2637C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2637 | chr18 | 49593159 | |||||
chr18:49593176 | G | A | 1 | a0001c0001t0123 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2654G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2654 | chr18 | 49593176 | |||||
chr18:49593209 | A | G | 55 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(52): Show | 123 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2687A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2687 | chr18 | 49593209 | |||||
chr18:49593241 | A | G | 2 | a0001c0001t0084a0001c0001t0085 | 2 | HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2719A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2719 | chr18 | 49593241 | |||||
chr18:49593283 | C | G | 1 | a0002c0002t0058 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2761 | chr18 | 49593283 | |||||
chr18:49593285 | G | A | 1 | a0001c0001t0085 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2763G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2763 | chr18 | 49593285 | |||||
chr18:49593344 | G | T | 3 | a0001c0001t0132a0002c0002t0060a0002c0012t0057 | 3 | HG02602.hp2 HG03704.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2822G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2822 | chr18 | 49593344 | |||||
chr18:49593373 | C | A | 2 | a0004c0006t0087a0004c0006t0088 | 2 | HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2851C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2851 | chr18 | 49593373 | |||||
chr18:49593570 | A | C | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3048A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3048 | chr18 | 49593570 | |||||
chr18:49593585 | G | C | 1 | a0001c0001t0090 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3063 | chr18 | 49593585 | |||||
chr18:49593690 | G | A | 1 | a0001c0001t0096 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3168G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3168 | chr18 | 49593690 | |||||
chr18:49593738 | G | C | 1 | a0002c0002t0072 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3216G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3216 | chr18 | 49593738 | |||||
chr18:49593787 | G | A | 1 | a0001c0001t0138 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3265G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3265 | chr18 | 49593787 | |||||
chr18:49593820 | T | C | 8 | a0001c0001t0033a0001c0001t0048a0001c0001t0081others(5): Show | 9 | HG00738.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3298T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3298 | chr18 | 49593820 | |||||
chr18:49593838 | C | T | 1 | a0001c0001t0056 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3316C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3316 | chr18 | 49593838 | |||||
chr18:49593936 | G | C | 2 | a0001c0001t0104a0001c0001t0105 | 2 | HG02647.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3414G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3414 | chr18 | 49593936 | |||||
chr18:49594121 | G | A | 1 | a0001c0001t0124 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3599G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3599 | chr18 | 49594121 | |||||
chr18:49594129 | T | G | 27 | a0001c0001t0002a0001c0001t0017a0001c0001t0034others(24): Show | 64 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3607T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3607 | chr18 | 49594129 | |||||
chr18:49594143 | G | GT | 17 | a0001c0001t0001a0001c0001t0015a0001c0001t0019others(14): Show | 65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3630dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3631 | INFO_REALIGN_3_PRIME | chr18 | 49594143 | ||||
chr18:49594193 | G | C | 6 | a0001c0001t0024a0001c0001t0032a0001c0001t0049others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3671G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3671 | chr18 | 49594193 | |||||
chr18:49594198 | G | C | 1 | a0002c0002t0058 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3676G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3676 | chr18 | 49594198 | |||||
chr18:49594230 | G | A | 49 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(46): Show | 115 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3708G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3708 | chr18 | 49594230 | |||||
chr18:49594403 | G | A | 1 | a0001c0001t0091 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3881G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3881 | chr18 | 49594403 | |||||
chr18:49594411 | C | T | 1 | a0002c0002t0074 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3889 | chr18 | 49594411 | |||||
chr18:49594425 | G | A | 2 | a0001c0001t0102a0001c0001t0106 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3903G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3903 | chr18 | 49594425 | |||||
chr18:49594441 | T | A | 1 | a0001c0001t0107 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3919 | chr18 | 49594441 | |||||
chr18:49594454 | C | T | 1 | a0001c0001t0084 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3932C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3932 | chr18 | 49594454 | |||||
chr18:49594490 | T | A | 3 | a0001c0001t0033a0001c0001t0083a0001c0001t0086 | 4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3968T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3968 | chr18 | 49594490 | |||||
chr18:49594520 | G | A | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3998G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3998 | chr18 | 49594520 | |||||
chr18:49594533 | C | T | 3 | a0001c0001t0033a0001c0001t0083a0001c0001t0086 | 4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4011C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4011 | chr18 | 49594533 | |||||
chr18:49594616 | A | T | 18 | a0001c0001t0001a0001c0001t0015a0001c0001t0019others(15): Show | 67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4094A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4094 | chr18 | 49594616 | |||||
chr18:49594623 | G | A | 6 | a0001c0001t0024a0001c0001t0032a0001c0001t0049others(3): Show | 9 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4101G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4101 | chr18 | 49594623 | |||||
chr18:49594747 | T | C | 5 | a0001c0001t0010a0001c0001t0042a0001c0001t0061others(2): Show | 12 | HG00639.hp2 HG01516.hp1 HG01943.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4225T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4225 | chr18 | 49594747 | |||||
chr18:49594946 | G | T | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(41): Show | 129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4424G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4424 | chr18 | 49594946 | |||||
chr18:49595201 | G | C | 5 | a0001c0001t0017a0001c0001t0078a0001c0001t0079others(2): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4679G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4679 | chr18 | 49595201 | |||||
chr18:49595267 | A | C | 2 | a0001c0001t0104a0001c0001t0105 | 2 | HG02647.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4745A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4745 | chr18 | 49595267 | |||||
chr18:49595306 | G | A | 1 | a0003c0004t0109 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4784G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4784 | chr18 | 49595306 | |||||
chr18:49595328 | A | G | 40 | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(37): Show | 112 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*4806A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4806 | chr18 | 49595328 | |||||
chr18:49595329 | G | T | 1 | a0001c0001t0137 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4807G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4807 | chr18 | 49595329 | |||||
chr18:49595412 | T | C | 3 | a0001c0001t0104a0001c0001t0105a0001c0001t0110 | 3 | HG02647.hp1 HG02896.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4890T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4890 | chr18 | 49595412 | |||||
chr18:49595606 | G | A | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5084G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5084 | chr18 | 49595606 | |||||
chr18:49595625 | C | T | 1 | a0001c0001t0096 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5103C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5103 | chr18 | 49595625 | |||||
chr18:49595689 | G | A | 1 | a0001c0001t0077 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5167G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5167 | chr18 | 49595689 | |||||
chr18:49595721 | C | T | 3 | a0001c0001t0048a0001c0001t0081a0001c0001t0082 | 3 | HG01243.hp2 HG03041.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5199C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5199 | chr18 | 49595721 | |||||
chr18:49595783 | A | G | 2 | a0001c0001t0084a0001c0001t0085 | 2 | HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5261A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5261 | chr18 | 49595783 | |||||
chr18:49595788 | A | C | 26 | a0001c0001t0002a0001c0001t0024a0001c0001t0032others(23): Show | 62 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*5266A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5266 | chr18 | 49595788 | |||||
chr18:49595904 | GGCCTATT others(44): Show |
G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5383_*5433delGCCT others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5383 | chr18 | 49595904 | |||||
chr18:49596272 | C | T | 2 | a0001c0001t0097a0001c0001t0098 | 2 | NA18944.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5750C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5750 | chr18 | 49596272 | |||||
chr18:49596362 | G | A | 4 | a0001c0001t0013a0001c0001t0043a0001c0001t0111others(1): Show | 10 | HG00609.hp1 HG01433.hp2 HG01978.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5840G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5840 | chr18 | 49596362 | |||||
chr18:49596484 | A | G | 26 | a0001c0001t0011a0001c0001t0038a0001c0001t0041others(23): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5962A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5962 | chr18 | 49596484 | |||||
chr18:49596551 | C | A | 36 | a0001c0001t0002a0001c0001t0008a0001c0001t0026others(33): Show | 93 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*6029C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6029 | chr18 | 49596551 | |||||
chr18:49596573 | T | G | 6 | a0001c0001t0010a0001c0001t0042a0001c0001t0061others(3): Show | 13 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6051T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6051 | chr18 | 49596573 | |||||
chr18:49596610 | G | T | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6088G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6088 | chr18 | 49596610 | |||||
chr18:49596635 | C | CA | 47 | a0001c0001t0008a0001c0001t0011a0001c0001t0026others(44): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*6136dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6137 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | ||||
chr18:49596635 | C | CAA | 10 | a0001c0001t0041a0001c0001t0049a0001c0001t0086others(7): Show | 12 | HG00423.hp1 HG00642.hp2 HG01358.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6135_*6136dupAA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6137 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | ||||
chr18:49596635 | CA | C | 8 | a0001c0001t0047a0001c0001t0078a0001c0001t0105others(5): Show | 9 | HG02155.hp1 HG02735.hp1 HG02735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6136delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6136 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | ||||
chr18:49596635 | CAAAAAA | C | 2 | a0003c0004t0016a0003c0004t0080 | 6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6131_*6136delAAAA others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6131 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | ||||
chr18:49596691 | A | G | 1 | a0001c0001t0136 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6169A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6169 | chr18 | 49596691 | |||||
chr18:49596752 | C | T | 28 | a0001c0001t0002a0001c0001t0008a0001c0001t0026others(25): Show | 76 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*6230C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6230 | chr18 | 49596752 | |||||
chr18:49596867 | T | C | 44 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(41): Show | 109 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*6345T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6345 | chr18 | 49596867 | |||||
chr18:49596928 | T | C | 2 | a0001c0001t0076a0001c0001t0077 | 2 | HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6406T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6406 | chr18 | 49596928 | |||||
chr18:49597393 | C | T | 32 | a0001c0001t0010a0001c0001t0011a0001c0001t0038others(29): Show | 71 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*6871C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6871 | chr18 | 49597393 | |||||
chr18:49597411 | C | G | 1 | a0002c0002t0064 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6889C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6889 | chr18 | 49597411 | |||||
chr18:49597489 | A | AAAGTCAA others(4): Show |
1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6968_*6969insAGTC others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6969 | INFO_REALIGN_3_PRIME | chr18 | 49597489 | ||||
chr18:49597492 | A | C | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6970A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6970 | chr18 | 49597492 | |||||
chr18:49597493 | T | A | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6971T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6971 | chr18 | 49597493 | |||||
chr18:49597496 | A | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6974A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6974 | chr18 | 49597496 | |||||
chr18:49597513 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6991T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6991 | chr18 | 49597513 | |||||
chr18:49597515 | G | GGAGGGCG others(20): Show |
1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6993_*6994insGAGG others(23): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6994 | chr18 | 49597515 | |||||
chr18:49597516 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6994T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6994 | chr18 | 49597516 | |||||
chr18:49597517 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6995T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6995 | chr18 | 49597517 | |||||
chr18:49597518 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6996T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6996 | chr18 | 49597518 | |||||
chr18:49597522 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7000T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7000 | chr18 | 49597522 | |||||
chr18:49597530 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7008T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7008 | chr18 | 49597530 | |||||
chr18:49597535 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7013T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7013 | chr18 | 49597535 | |||||
chr18:49597538 | T | C | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7016T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7016 | chr18 | 49597538 | |||||
chr18:49597539 | C | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7017C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7017 | chr18 | 49597539 | |||||
chr18:49597551 | A | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7029A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7029 | chr18 | 49597551 | |||||
chr18:49597552 | C | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7030C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7030 | chr18 | 49597552 | |||||
chr18:49597555 | T | A | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7033T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7033 | chr18 | 49597555 | |||||
chr18:49597556 | G | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7034G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7034 | chr18 | 49597556 | |||||
chr18:49597557 | A | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7035A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7035 | chr18 | 49597557 | |||||
chr18:49597562 | C | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7040C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7040 | chr18 | 49597562 | |||||
chr18:49597634 | G | T | 1 | a0001c0001t0112 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7112G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7112 | chr18 | 49597634 | |||||
chr18:49597668 | G | A | 12 | a0001c0001t0018a0001c0001t0096a0001c0001t0135others(9): Show | 31 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*7146G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7146 | chr18 | 49597668 | |||||
chr18:49598211 | T | C | 4 | a0001c0001t0026a0002c0002t0014a0003c0004t0026others(1): Show | 9 | HG01884.hp1 HG02109.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7689T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7689 | chr18 | 49598211 | |||||
chr18:49598218 | A | G | 1 | a0001c0001t0083 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7696A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7696 | chr18 | 49598218 | |||||
chr18:49598255 | C | T | 1 | a0001c0001t0095 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7733C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7733 | chr18 | 49598255 | |||||
chr18:49598271 | T | G | 2 | a0001c0001t0131a0002c0002t0021 | 4 | HG00323.hp2 HG01167.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7749T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7749 | chr18 | 49598271 | |||||
chr18:49598538 | C | T | 4 | a0001c0001t0094a0001c0001t0104a0001c0001t0105others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8016C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8016 | chr18 | 49598538 | |||||
chr18:49598612 | C | G | 15 | a0001c0001t0002a0001c0001t0034a0001c0001t0035others(12): Show | 49 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*8090C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8090 | chr18 | 49598612 | |||||
chr18:49598616 | T | G | 1 | a0001c0001t0119 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8094T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8094 | chr18 | 49598616 | |||||
chr18:49599002 | G | A | 37 | a0001c0001t0010a0001c0001t0011a0001c0001t0032others(34): Show | 77 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*8480G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8480 | chr18 | 49599002 | |||||
chr18:49599055 | T | C | 2 | a0001c0001t0102a0001c0001t0106 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8533T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8533 | chr18 | 49599055 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:49562451 | G | A | 3 | a0001c0001t0011g0005a0001c0001t0011g0006a0001c0001t0041g0004 | 3 | HG01109.hp1 HG01192.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.97+46G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562451 | ||||||
chr18:49562456 | C | T | 87 | a0001c0001t0020g0375a0001c0001t0052g0374a0001c0001t0053g0338others(84): Show | 88 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.97+51C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562456 | ||||||
chr18:49562460 | C | G | 87 | a0001c0001t0020g0375a0001c0001t0052g0374a0001c0001t0053g0338others(84): Show | 88 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.97+55C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562460 | ||||||
chr18:49562512 | C | T | 3 | a0001c0001t0008g0293a0001c0001t0119g0294a0006c0008t0008g0295 | 3 | HG00423.hp1 HG00544.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.97+107C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562512 | ||||||
chr18:49562545 | C | G | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+140C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562545 | ||||||
chr18:49562705 | G | T | 1 | a0002c0002t0062g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97+300G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562705 | ||||||
chr18:49562707 | C | T | 52 | a0001c0001t0020g0375a0001c0001t0052g0374a0001c0001t0053g0338others(49): Show | 53 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.97+302C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562707 | ||||||
chr18:49562728 | T | C | 16 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(13): Show | 16 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+323T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562728 | ||||||
chr18:49562823 | G | C | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+418G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562823 | ||||||
chr18:49562872 | G | A | 9 | a0001c0001t0015g0001a0001c0001t0015g0023a0001c0001t0015g0024others(6): Show | 10 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+467G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562872 | ||||||
chr18:49563316 | G | C | 6 | a0002c0002t0014g0332a0002c0002t0014g0333a0002c0002t0014g0334others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+911G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563316 | ||||||
chr18:49563371 | C | T | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+966C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563371 | ||||||
chr18:49563430 | A | G | 1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.97+1025A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563430 | ||||||
chr18:49563442 | G | A | 1 | a0001c0001t0077g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+1037G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563442 | ||||||
chr18:49563458 | T | C | 1 | a0001c0001t0053g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.97+1053T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563458 | ||||||
chr18:49563547 | AAGAC | A | 7 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+1149_97+1152del others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 49563547 | |||||
chr18:49563601 | A | G | 5 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0283others(2): Show | 5 | HG01069.hp1 HG01070.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+1196A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563601 | ||||||
chr18:49563616 | G | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97+1211G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563616 | ||||||
chr18:49563623 | G | A | 1 | a0001c0001t0077g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+1218G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563623 | ||||||
chr18:49563691 | G | C | 1 | a0007c0007t0026g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.97+1286G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563691 | ||||||
chr18:49563722 | A | G | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+1317A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563722 | ||||||
chr18:49563805 | T | C | 12 | a0001c0001t0003g0041a0001c0001t0006g0034a0001c0001t0006g0037others(9): Show | 12 | HG00099.hp2 HG01074.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+1400T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563805 | ||||||
chr18:49563889 | G | C | 7 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-1428G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563889 | ||||||
chr18:49563921 | A | G | 2 | a0001c0001t0001g0278a0001c0001t0131g0279 | 2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.98-1396A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563921 | ||||||
chr18:49564031 | T | C | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98-1286T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564031 | ||||||
chr18:49564131 | C | T | 1 | a0001c0001t0015g0001 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.98-1186C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564131 | ||||||
chr18:49564361 | G | A | 1 | a0002c0002t0005g0339 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.98-956G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564361 | ||||||
chr18:49564442 | T | C | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-875T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564442 | ||||||
chr18:49564551 | C | A | 1 | a0001c0001t0077g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98-766C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564551 | ||||||
chr18:49564659 | A | C | 1 | a0001c0001t0011g0277 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.98-658A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564659 | ||||||
chr18:49564858 | C | T | 1 | a0002c0002t0064g0379 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.98-459C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564858 | ||||||
chr18:49564915 | C | T | 15 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(12): Show | 15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-402C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564915 | ||||||
chr18:49564989 | C | T | 18 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(15): Show | 18 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.98-328C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564989 | ||||||
chr18:49564996 | C | T | 1 | a0001c0001t0085g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.98-321C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564996 | ||||||
chr18:49565037 | T | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.98-280T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565037 | ||||||
chr18:49565147 | A | G | 18 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(15): Show | 18 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.98-170A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565147 | ||||||
chr18:49565207 | G | A | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-110G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565207 | ||||||
chr18:49565258 | C | T | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.98-59C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565258 | ||||||
chr18:49565605 | C | G | 4 | a0002c0002t0004g0330a0002c0002t0023g0329a0002c0002t0069g0331others(1): Show | 4 | NA18962.hp1 NA19055.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+107C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49565605 | ||||||
chr18:49565820 | G | T | 1 | a0001c0001t0003g0262 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.279+322G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49565820 | ||||||
chr18:49565958 | A | G | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0036g0259 | 3 | NA18975.hp1 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.279+460A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49565958 | ||||||
chr18:49566007 | G | A | 1 | a0001c0001t0006g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.279+509G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566007 | ||||||
chr18:49566100 | T | G | 6 | a0002c0002t0014g0332a0002c0002t0014g0333a0002c0002t0014g0334others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+602T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566100 | ||||||
chr18:49566109 | A | G | 2 | a0001c0001t0084g0258a0001c0001t0085g0263 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+611A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566109 | ||||||
chr18:49566138 | C | G | 2 | a0001c0001t0094g0030a0001c0001t0096g0029 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.279+640C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566138 | ||||||
chr18:49566157 | A | AC | 3 | a0002c0002t0021g0376a0002c0002t0021g0377a0002c0002t0021g0378 | 3 | HG01167.hp1 HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.279+660dupC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 49566157 | |||||
chr18:49566256 | G | A | 1 | a0001c0001t0044g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.279+758G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566256 | ||||||
chr18:49566450 | C | T | 2 | a0001c0001t0002g0256a0001c0001t0092g0257 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.279+952C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566450 | ||||||
chr18:49566493 | T | C | 3 | a0001c0001t0049g0292a0001c0001t0097g0267a0001c0001t0098g0268 | 3 | NA18944.hp2 NA19030.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.280-949T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566493 | ||||||
chr18:49566500 | C | G | 1 | a0005c0010t0010g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.280-942C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566500 | ||||||
chr18:49566556 | G | T | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-886G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566556 | ||||||
chr18:49566761 | A | G | 3 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274 | 3 | HG00738.hp1 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.280-681A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566761 | ||||||
chr18:49566811 | A | G | 1 | a0001c0001t0025g0254 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280-631A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566811 | ||||||
chr18:49566942 | G | A | 18 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(15): Show | 18 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.280-500G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566942 | ||||||
chr18:49566967 | G | A | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-475G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566967 | ||||||
chr18:49566992 | T | G | 1 | a0002c0002t0005g0340 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280-450T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566992 | ||||||
chr18:49567012 | G | T | 1 | a0001c0001t0089g0253 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.280-430G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567012 | ||||||
chr18:49567074 | C | T | 12 | a0001c0001t0003g0041a0001c0001t0006g0034a0001c0001t0006g0037others(9): Show | 12 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-368C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567074 | ||||||
chr18:49567107 | T | C | 2 | a0001c0001t0006g0037a0001c0001t0006g0038 | 2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.280-335T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567107 | ||||||
chr18:49567309 | C | T | 1 | a0001c0001t0011g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280-133C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567309 | ||||||
chr18:49567420 | C | T | 273 | a0001c0001t0001g0175a0001c0001t0001g0206a0001c0001t0001g0208others(270): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.280-22C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567420 | ||||||
chr18:49567866 | T | C | 2 | a0001c0001t0012g0051a0001c0001t0127g0050 | 2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.459+245T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49567866 | ||||||
chr18:49567979 | TGAAGCAT others(18): Show |
T | 3 | a0001c0001t0015g0001a0001c0001t0015g0027a0001c0001t0015g0028 | 4 | HG00642.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+361_459+385del others(25): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 49567979 | |||||
chr18:49568052 | T | C | 273 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(270): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.459+431T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568052 | ||||||
chr18:49568072 | C | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(30): Show | 33 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+451C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568072 | ||||||
chr18:49568157 | G | A | 2 | a0002c0002t0005g0341a0002c0002t0051g0342 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.459+536G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568157 | ||||||
chr18:49568175 | C | G | 19 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(16): Show | 19 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.459+554C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568175 | ||||||
chr18:49568413 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.459+792C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568413 | ||||||
chr18:49568434 | G | A | 9 | a0001c0001t0002g0054a0001c0001t0003g0056a0001c0001t0003g0058others(6): Show | 9 | HG02040.hp1 HG02080.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+813G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568434 | ||||||
chr18:49568479 | C | T | 1 | a0001c0001t0017g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459+858C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568479 | ||||||
chr18:49568512 | C | A | 1 | a0001c0001t0006g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+891C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568512 | ||||||
chr18:49568543 | A | G | 1 | a0002c0002t0074g0373 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.460-894A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568543 | ||||||
chr18:49568872 | CCTAAGCT others(3): Show |
C | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.460-561_460-552del others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 49568872 | |||||
chr18:49568883 | C | G | 1 | a0001c0001t0077g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460-554C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568883 | ||||||
chr18:49568928 | C | CA | 4 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-508dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 49568928 | |||||
chr18:49568956 | C | A | 13 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(10): Show | 13 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.460-481C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568956 | ||||||
chr18:49569050 | A | G | 274 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(271): Show | 277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.460-387A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569050 | ||||||
chr18:49569117 | T | C | 183 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.460-320T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569117 | ||||||
chr18:49569204 | C | G | 13 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(10): Show | 13 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.460-233C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569204 | ||||||
chr18:49569210 | C | T | 1 | a0002c0002t0073g0372 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.460-227C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569210 | ||||||
chr18:49569225 | T | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.460-212T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569225 | ||||||
chr18:49569305 | G | T | 1 | a0001c0001t0019g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.460-132G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569305 | ||||||
chr18:49569606 | C | T | 13 | a0001c0001t0026g0270a0001c0001t0033g0275a0001c0001t0033g0276others(10): Show | 13 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+58C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569606 | ||||||
chr18:49569646 | G | A | 45 | a0001c0001t0102g0143a0001c0001t0106g0144a0002c0002t0005g0003others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.571+98G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569646 | ||||||
chr18:49569705 | C | CT | 91 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0018g0141others(88): Show | 92 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.571+171dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49569705 | |||||
chr18:49569733 | G | A | 1 | a0002c0002t0028g0343 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.571+185G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569733 | ||||||
chr18:49569829 | G | A | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.571+281G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569829 | ||||||
chr18:49569868 | C | G | 1 | a0001c0001t0079g0289 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571+320C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569868 | ||||||
chr18:49569924 | G | A | 29 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(26): Show | 29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+376G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569924 | ||||||
chr18:49569948 | G | A | 4 | a0003c0004t0016g0145a0003c0004t0016g0146a0003c0004t0016g0148others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+400G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569948 | ||||||
chr18:49570131 | G | C | 25 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(22): Show | 25 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.571+583G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570131 | ||||||
chr18:49570145 | G | A | 1 | a0001c0001t0086g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.571+597G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570145 | ||||||
chr18:49570169 | G | A | 1 | a0001c0001t0120g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.571+621G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570169 | ||||||
chr18:49570215 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.571+667G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570215 | ||||||
chr18:49570221 | A | G | 25 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(22): Show | 25 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.571+673A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570221 | ||||||
chr18:49570381 | T | TTAATGGT others(21): Show |
1 | a0002c0013t0004g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.571+836_571+863dup others(28): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49570381 | |||||
chr18:49570612 | C | T | 65 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(62): Show | 66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.571+1064C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570612 | ||||||
chr18:49570698 | G | A | 1 | a0002c0002t0130g0171 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.571+1150G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570698 | ||||||
chr18:49570826 | C | CTCAAAAA others(16): Show |
1 | a0002c0012t0057g0368 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571+1279_571+1301d others(25): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49570826 | |||||
chr18:49570876 | C | T | 1 | a0001c0001t0129g0138 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.571+1328C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570876 | ||||||
chr18:49570921 | T | C | 9 | a0001c0001t0011g0005a0001c0001t0011g0006a0001c0001t0011g0062others(6): Show | 9 | HG01109.hp1 HG01192.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+1373T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570921 | ||||||
chr18:49571002 | G | A | 10 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0209others(7): Show | 10 | HG00280.hp1 HG00323.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.571+1454G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571002 | ||||||
chr18:49571028 | A | G | 29 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(26): Show | 29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+1480A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571028 | ||||||
chr18:49571051 | C | G | 1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1503C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571051 | ||||||
chr18:49571119 | C | T | 166 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.571+1571C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571119 | ||||||
chr18:49571193 | A | T | 4 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+1645A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571193 | ||||||
chr18:49571205 | T | C | 29 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(26): Show | 29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+1657T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571205 | ||||||
chr18:49571212 | A | G | 1 | a0002c0002t0005g0371 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.571+1664A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571212 | ||||||
chr18:49571241 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.571+1693G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571241 | ||||||
chr18:49571254 | G | T | 1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1706G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571254 | ||||||
chr18:49571313 | T | C | 29 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(26): Show | 29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+1765T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571313 | ||||||
chr18:49571456 | A | G | 1 | a0001c0001t0003g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.571+1908A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571456 | ||||||
chr18:49571463 | C | G | 1 | a0001c0001t0003g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.571+1915C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571463 | ||||||
chr18:49571476 | T | A | 1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1928T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571476 | ||||||
chr18:49571483 | T | C | 13 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.571+1935T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571483 | ||||||
chr18:49571558 | A | G | 1 | a0001c0001t0061g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571+2010A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571558 | ||||||
chr18:49571693 | G | A | 8 | a0001c0001t0006g0008a0001c0001t0038g0025a0001c0001t0038g0172others(5): Show | 8 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+2145G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571693 | ||||||
chr18:49571702 | A | C | 4 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274others(1): Show | 4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+2154A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571702 | ||||||
chr18:49571866 | G | C | 1 | a0001c0001t0052g0374 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.571+2318G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571866 | ||||||
chr18:49571873 | GAGAGAAG others(11): Show |
G | 1 | a0002c0012t0057g0368 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571+2328_571+2345d others(20): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49571873 | |||||
chr18:49571899 | A | G | 1 | a0001c0001t0010g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571+2351A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571899 | ||||||
chr18:49571918 | G | C | 2 | a0002c0002t0004g0298a0002c0002t0004g0299 | 2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571+2370G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571918 | ||||||
chr18:49571986 | T | C | 4 | a0002c0002t0021g0376a0002c0002t0021g0377a0002c0002t0021g0378others(1): Show | 4 | HG01167.hp1 HG01346.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+2438T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571986 | ||||||
chr18:49572031 | C | T | 18 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(15): Show | 18 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.571+2483C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572031 | ||||||
chr18:49572112 | G | A | 1 | a0001c0001t0011g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.571+2564G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572112 | ||||||
chr18:49572158 | A | G | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.571+2610A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572158 | ||||||
chr18:49572248 | A | G | 1 | a0001c0001t0003g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.571+2700A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572248 | ||||||
chr18:49572256 | GT | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | NA18960.hp2 NA18964.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+2710delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572256 | |||||
chr18:49572276 | C | T | 9 | a0001c0001t0032g0021a0001c0001t0032g0022a0003c0004t0016g0145others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+2728C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572276 | ||||||
chr18:49572320 | CAAAAATA | C | 66 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(63): Show | 67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.571+2792_571+2798d others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572320 | |||||
chr18:49572333 | T | A | 1 | a0001c0001t0003g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.571+2785T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572333 | ||||||
chr18:49572333 | TAAAA | T | 27 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.571+2788_571+2791d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572333 | |||||
chr18:49572361 | A | G | 2 | a0001c0001t0084g0258a0001c0001t0085g0263 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.571+2813A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572361 | ||||||
chr18:49572370 | A | G | 1 | a0001c0001t0017g0288 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.571+2822A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572370 | ||||||
chr18:49572386 | A | G | 2 | a0001c0001t0001g0175a0001c0001t0019g0248 | 2 | NA18968.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.571+2838A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572386 | ||||||
chr18:49572422 | C | A | 1 | a0001c0001t0012g0069 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.571+2874C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572422 | ||||||
chr18:49572490 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.572-2879A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572490 | ||||||
chr18:49572714 | G | C | 46 | a0001c0001t0102g0143a0001c0001t0106g0144a0002c0002t0005g0003others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.572-2655G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572714 | ||||||
chr18:49572730 | T | TA | 7 | a0001c0001t0003g0061a0001c0001t0003g0070a0001c0001t0003g0139others(4): Show | 7 | HG00140.hp2 HG03654.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.572-2617dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | |||||
chr18:49572730 | TA | T | 22 | a0001c0001t0001g0218a0001c0001t0002g0134a0001c0001t0002g0135others(19): Show | 22 | HG00609.hp1 HG01975.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.572-2617delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | |||||
chr18:49572730 | TAA | T | 201 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(198): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.572-2618_572-2617d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | |||||
chr18:49572730 | TAAA | T | 43 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(40): Show | 43 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.572-2619_572-2617d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | |||||
chr18:49572730 | TAAAA | T | 16 | a0001c0001t0010g0151a0001c0001t0010g0152a0001c0001t0010g0155others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.572-2620_572-2617d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | |||||
chr18:49572814 | T | TTACATGT others(16): Show |
1 | a0001c0001t0011g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.572-2553_572-2531d others(25): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572814 | |||||
chr18:49572816 | A | G | 38 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(35): Show | 38 | HG00639.hp2 HG00735.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.572-2553A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572816 | ||||||
chr18:49572831 | T | C | 1 | a0001c0001t0135g0220 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.572-2538T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572831 | ||||||
chr18:49573024 | G | T | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.572-2345G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573024 | ||||||
chr18:49573073 | C | G | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.572-2296C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573073 | ||||||
chr18:49573184 | T | G | 1 | a0001c0001t0084g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.572-2185T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573184 | ||||||
chr18:49573287 | G | T | 1 | a0001c0001t0006g0008 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.572-2082G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573287 | ||||||
chr18:49573294 | C | G | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129 | 3 | NA18990.hp1 NA19004.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.572-2075C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573294 | ||||||
chr18:49573302 | G | GGTTGTCG others(6): Show |
1 | a0001c0001t0001g0052 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.572-2063_572-2051d others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49573302 | |||||
chr18:49573304 | T | C | 11 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.572-2065T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573304 | ||||||
chr18:49573309 | G | A | 3 | a0001c0001t0027g0240a0001c0001t0138g0221a0002c0002t0067g0327 | 3 | NA18947.hp2 NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.572-2060G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573309 | ||||||
chr18:49573326 | C | G | 1 | a0001c0001t0082g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.572-2043C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573326 | ||||||
chr18:49573329 | A | G | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.572-2040A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573329 | ||||||
chr18:49573355 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.572-2014G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573355 | ||||||
chr18:49573491 | A | C | 17 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(14): Show | 17 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.572-1878A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573491 | ||||||
chr18:49573512 | G | A | 1 | a0001c0001t0095g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.572-1857G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573512 | ||||||
chr18:49573572 | T | A | 1 | a0002c0002t0004g0300 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.572-1797T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573572 | ||||||
chr18:49573576 | A | T | 27 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.572-1793A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573576 | ||||||
chr18:49573579 | C | CA | 6 | a0001c0001t0001g0052a0001c0001t0011g0277a0001c0001t0015g0027others(3): Show | 6 | HG01981.hp1 NA18944.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.572-1777dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49573579 | |||||
chr18:49573579 | CA | C | 9 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.572-1777delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49573579 | |||||
chr18:49573644 | C | T | 1 | a0001c0001t0015g0001 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.572-1725C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573644 | ||||||
chr18:49573793 | A | C | 25 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(22): Show | 25 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.572-1576A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573793 | ||||||
chr18:49573915 | G | T | 84 | a0001c0001t0018g0141a0001c0001t0077g0031a0001c0001t0102g0143others(81): Show | 85 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.572-1454G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573915 | ||||||
chr18:49573928 | G | A | 3 | a0001c0001t0013g0131a0001c0001t0018g0071a0001c0001t0018g0130 | 3 | HG00609.hp1 NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.572-1441G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573928 | ||||||
chr18:49574093 | C | T | 6 | a0001c0001t0003g0061a0001c0001t0003g0068a0001c0001t0003g0070others(3): Show | 6 | NA18941.hp2 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.572-1276C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574093 | ||||||
chr18:49574235 | GGCACTCA others(4): Show |
G | 1 | a0001c0001t0010g0149 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.572-1133_572-1123d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574235 | ||||||
chr18:49574293 | C | T | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.572-1076C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574293 | ||||||
chr18:49574429 | C | T | 7 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572-940C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574429 | ||||||
chr18:49574456 | G | A | 2 | a0001c0001t0015g0023a0001c0001t0015g0024 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.572-913G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574456 | ||||||
chr18:49574670 | A | T | 83 | a0001c0001t0018g0141a0001c0001t0077g0031a0001c0001t0102g0143others(80): Show | 84 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.572-699A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574670 | ||||||
chr18:49574880 | G | A | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-489G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574880 | ||||||
chr18:49574977 | G | T | 1 | a0002c0013t0004g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.572-392G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574977 | ||||||
chr18:49575061 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.572-308T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575061 | ||||||
chr18:49575219 | T | C | 14 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.572-150T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575219 | ||||||
chr18:49575235 | T | G | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-134T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575235 | ||||||
chr18:49575284 | C | T | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.572-85C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575284 | ||||||
chr18:49575326 | G | A | 1 | a0001c0001t0017g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.572-43G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575326 | ||||||
chr18:49575598 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | splice_region_variant&intron_variant | LOW | c.793+8C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575598 | ||||||
chr18:49575632 | T | C | 202 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(199): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.793+42T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575632 | ||||||
chr18:49575673 | G | A | 2 | a0002c0002t0005g0346a0002c0002t0005g0365 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793+83G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575673 | ||||||
chr18:49575732 | A | G | 276 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(273): Show | 279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.793+142A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575732 | ||||||
chr18:49575747 | C | T | 6 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+157C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575747 | ||||||
chr18:49575817 | ATTTCT | A | 76 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(73): Show | 77 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.793+241_793+245del others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49575817 | |||||
chr18:49575833 | T | C | 1 | a0001c0001t0128g0040 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.793+243T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575833 | ||||||
chr18:49575841 | C | CT | 13 | a0001c0001t0001g0052a0001c0001t0006g0122a0001c0001t0012g0069others(10): Show | 13 | HG00140.hp2 HG01168.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.793+265dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49575841 | |||||
chr18:49575853 | T | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+263T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575853 | ||||||
chr18:49575945 | T | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+355T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575945 | ||||||
chr18:49575986 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+396G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575986 | ||||||
chr18:49576037 | C | T | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+447C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576037 | ||||||
chr18:49576127 | C | T | 1 | a0001c0001t0048g0271 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793+537C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576127 | ||||||
chr18:49576128 | G | A | 2 | a0001c0001t0012g0051a0001c0001t0127g0050 | 2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.793+538G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576128 | ||||||
chr18:49576133 | C | T | 86 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(83): Show | 87 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.793+543C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576133 | ||||||
chr18:49576223 | C | T | 1 | a0001c0001t0037g0136 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.793+633C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576223 | ||||||
chr18:49576272 | A | G | 4 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+682A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576272 | ||||||
chr18:49576332 | T | C | 3 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0049g0292 | 3 | HG01891.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.793+742T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576332 | ||||||
chr18:49576338 | A | C | 1 | a0002c0012t0057g0368 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.793+748A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576338 | ||||||
chr18:49576339 | A | G | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+749A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576339 | ||||||
chr18:49576428 | CTTTTCTT others(4): Show |
C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+840_793+850del others(11): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576428 | |||||
chr18:49576433 | CT | C | 5 | a0001c0001t0003g0061a0001c0001t0102g0143a0002c0002t0067g0327others(2): Show | 5 | HG01257.hp2 HG02602.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+850delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576433 | |||||
chr18:49576457 | C | CT | 54 | a0001c0001t0001g0223a0001c0001t0002g0033a0001c0001t0002g0103others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.793+894dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTT | 48 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.793+893_793+894dup others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTT | 26 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0214others(23): Show | 26 | HG00438.hp1 HG00642.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.793+892_793+894dup others(3): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTT | 13 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(10): Show | 13 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.793+891_793+894dup others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTT | 21 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(18): Show | 21 | HG00735.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.793+890_793+894dup others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTT | 14 | a0001c0001t0003g0018a0001c0001t0006g0008a0001c0001t0008g0002others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.793+889_793+894dup others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTTT | 8 | a0001c0001t0006g0037a0001c0001t0008g0192a0001c0001t0008g0193others(5): Show | 8 | HG00544.hp2 HG01261.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+888_793+894dup others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTTT others(1): Show |
13 | a0001c0001t0003g0041a0001c0001t0006g0042a0001c0001t0006g0043others(10): Show | 13 | HG00099.hp2 HG00423.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.793+887_793+894dup others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0044others(6): Show | 9 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.793+886_793+894dup others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0020g0375a0001c0001t0044g0035a0001c0001t0115g0045others(2): Show | 5 | HG00733.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+885_793+894dup others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTTT others(5): Show |
1 | a0006c0008t0008g0295 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.793+883_793+894dup others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0006g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.793+882_793+894dup others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | CTTTTTT | C | 7 | a0001c0001t0041g0160a0001c0001t0097g0267a0001c0001t0098g0268others(4): Show | 7 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+889_793+894del others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0018g0141a0002c0002t0005g0346a0002c0002t0009g0360others(6): Show | 9 | HG00140.hp1 HG01071.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+885_793+894del others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | CTTTTTTT others(4): Show |
C | 76 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0077g0031others(73): Show | 77 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.793+884_793+894del others(11): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0014g0332 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793+883_793+894del others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576457 | CTTTTTTT others(8): Show |
C | 11 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+880_793+894del others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | |||||
chr18:49576531 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+941G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576531 | ||||||
chr18:49576532 | A | C | 4 | a0002c0002t0005g0340a0002c0002t0005g0346a0002c0002t0005g0365others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+942A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576532 | ||||||
chr18:49576627 | C | A | 85 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(82): Show | 86 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.793+1037C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576627 | ||||||
chr18:49576628 | C | A | 1 | a0002c0013t0004g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+1038C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576628 | ||||||
chr18:49576783 | T | C | 2 | a0002c0002t0004g0370a0002c0002t0065g0369 | 2 | HG02155.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.793+1193T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576783 | ||||||
chr18:49576836 | T | TCCTGGGC others(12): Show |
1 | a0002c0012t0057g0368 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.793+1251_793+1269d others(21): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576836 | |||||
chr18:49576846 | A | C | 2 | a0001c0001t0094g0030a0001c0001t0096g0029 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.793+1256A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576846 | ||||||
chr18:49576908 | T | G | 7 | a0001c0001t0010g0151a0001c0001t0010g0155a0001c0001t0010g0158others(4): Show | 7 | HG03017.hp2 HG03654.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+1318T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576908 | ||||||
chr18:49577012 | T | TTTTATTT others(2): Show |
3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1425_793+1426i others(11): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577012 | |||||
chr18:49577022 | A | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1432A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577022 | ||||||
chr18:49577024 | T | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1434T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577024 | ||||||
chr18:49577025 | T | A | 16 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(13): Show | 16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+1435T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577025 | ||||||
chr18:49577026 | A | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1436A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577026 | ||||||
chr18:49577030 | T | A | 23 | a0001c0001t0001g0206a0001c0001t0003g0041a0001c0001t0006g0034others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.793+1440T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577030 | ||||||
chr18:49577030 | T | TTTTTTTA others(17): Show |
1 | a0001c0001t0010g0149 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.793+1444_793+1467d others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577030 | |||||
chr18:49577099 | A | T | 38 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(35): Show | 38 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.793+1509A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577099 | ||||||
chr18:49577162 | T | C | 275 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(272): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.793+1572T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577162 | ||||||
chr18:49577189 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.793+1599A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577189 | ||||||
chr18:49577190 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.793+1600T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577190 | ||||||
chr18:49577239 | C | T | 1 | a0001c0001t0010g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.793+1649C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577239 | ||||||
chr18:49577259 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.793+1669C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577259 | ||||||
chr18:49577324 | A | G | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.793+1734A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577324 | ||||||
chr18:49577455 | C | CT | 3 | a0001c0001t0025g0254a0001c0001t0026g0270a0001c0001t0048g0271 | 3 | HG01243.hp2 HG01884.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.793+1869dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577455 | |||||
chr18:49577479 | C | T | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+1889C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577479 | ||||||
chr18:49577491 | G | A | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+1901G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577491 | ||||||
chr18:49577501 | T | C | 2 | a0004c0006t0029g0265a0004c0006t0029g0266 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1911T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577501 | ||||||
chr18:49577507 | T | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+1917T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577507 | ||||||
chr18:49577513 | G | T | 6 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0006g0008others(3): Show | 6 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+1923G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577513 | ||||||
chr18:49577528 | C | T | 1 | a0001c0001t0044g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793+1938C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577528 | ||||||
chr18:49577546 | C | CG | 17 | a0001c0001t0001g0052a0001c0001t0001g0284a0001c0001t0002g0103others(14): Show | 17 | HG01346.hp1 HG01361.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.793+1960dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577546 | |||||
chr18:49577546 | C | T | 2 | a0001c0001t0038g0025a0001c0001t0038g0172 | 2 | HG02071.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.793+1956C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577546 | ||||||
chr18:49577592 | G | A | 2 | a0001c0001t0084g0258a0001c0001t0085g0263 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.793+2002G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577592 | ||||||
chr18:49577595 | C | CG | 5 | a0001c0001t0001g0052a0001c0001t0011g0062a0001c0001t0012g0069others(2): Show | 5 | HG00140.hp2 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+2008dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577595 | |||||
chr18:49577606 | A | G | 13 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0041g0160others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.793+2016A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577606 | ||||||
chr18:49577616 | T | TCCC | 40 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(37): Show | 40 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.793+2027_793+2029d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577616 | |||||
chr18:49577619 | C | CGGATGGG others(575): Show |
3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2032_793+2033i others(584): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577619 | |||||
chr18:49577619 | C | T | 1 | a0001c0001t0056g0296 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.793+2029C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577619 | ||||||
chr18:49577619 | CGGACGGG others(318): Show |
C | 62 | a0001c0001t0003g0041a0001c0001t0006g0034a0001c0001t0006g0037others(59): Show | 63 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.793+2116_793+2440d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577619 | |||||
chr18:49577624 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2034G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577624 | ||||||
chr18:49577624 | G | C | 18 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(15): Show | 18 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.793+2034G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577624 | ||||||
chr18:49577625 | GGGCGGCT others(4): Show |
G | 1 | a0001c0001t0002g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.793+2038_793+2048d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577625 | |||||
chr18:49577657 | CACCTCCC others(42): Show |
C | 20 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0052g0374others(17): Show | 20 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.793+2082_793+2130d others(51): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577657 | |||||
chr18:49577661 | T | C | 1 | a0001c0001t0048g0271 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793+2071T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577661 | ||||||
chr18:49577662 | C | A | 1 | a0001c0001t0048g0271 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793+2072C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577662 | ||||||
chr18:49577667 | C | T | 6 | a0003c0004t0016g0145a0003c0004t0016g0146a0003c0004t0016g0148others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+2077C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577667 | ||||||
chr18:49577669 | G | C | 16 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(13): Show | 16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+2079G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577669 | ||||||
chr18:49577673 | G | A | 1 | a0001c0001t0012g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.793+2083G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577673 | ||||||
chr18:49577676 | ACGGCTGG others(141): Show |
A | 12 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.793+2096_793+2243d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577676 | |||||
chr18:49577677 | C | T | 1 | a0002c0002t0004g0318 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.793+2087C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577677 | ||||||
chr18:49577683 | G | T | 9 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+2093G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577683 | ||||||
chr18:49577686 | A | G | 1 | a0002c0002t0021g0378 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.793+2096A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577686 | ||||||
chr18:49577689 | CGGGGGGC others(43): Show |
C | 4 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0094g0030others(1): Show | 4 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+2116_793+2165d others(52): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577689 | |||||
chr18:49577700 | CCCCCCAA others(317): Show |
C | 1 | a0001c0005t0007g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793+2116_793+2439d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577700 | |||||
chr18:49577706 | A | C | 110 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(107): Show | 111 | HG00558.hp2 HG00609.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.793+2116A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577706 | ||||||
chr18:49577724 | C | G | 1 | a0002c0002t0021g0378 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.793+2134C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577724 | ||||||
chr18:49577725 | A | G | 4 | a0002c0002t0004g0302a0002c0002t0018g0173a0002c0002t0021g0378others(1): Show | 4 | HG01167.hp1 HG02015.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+2135A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577725 | ||||||
chr18:49577735 | G | A | 3 | a0001c0001t0097g0267a0001c0001t0098g0268a0002c0002t0021g0378 | 3 | HG01167.hp1 NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+2145G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577735 | ||||||
chr18:49577738 | C | CG | 11 | a0001c0001t0002g0260a0001c0001t0011g0005a0001c0001t0012g0069others(8): Show | 11 | HG00140.hp2 HG01175.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+2155dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577738 | |||||
chr18:49577738 | C | T | 1 | a0001c0001t0137g0100 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.793+2148C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577738 | ||||||
chr18:49577739 | GGGGGGGC others(317): Show |
G | 1 | a0001c0001t0101g0191 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.793+2156_793+2479d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577739 | |||||
chr18:49577749 | AC | A | 104 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(101): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.793+2166delC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577749 | |||||
chr18:49577768 | G | GGACACGG others(120): Show |
3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2180_793+2181i others(129): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577768 | |||||
chr18:49577771 | T | C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2181T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577771 | ||||||
chr18:49577785 | A | G | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2195A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577785 | ||||||
chr18:49577788 | C | CG | 8 | a0001c0001t0001g0246a0001c0001t0003g0016a0001c0001t0003g0139others(5): Show | 8 | HG01516.hp2 HG02602.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.793+2204dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577788 | |||||
chr18:49577791 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2201G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577791 | ||||||
chr18:49577798 | A | AC | 10 | a0001c0001t0001g0229a0001c0001t0002g0103a0001c0001t0003g0121others(7): Show | 10 | HG00140.hp2 HG01243.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+2215dupC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577798 | |||||
chr18:49577803 | C | G | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.793+2213C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577803 | ||||||
chr18:49577805 | C | A | 1 | a0002c0013t0004g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+2215C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577805 | ||||||
chr18:49577810 | CCCTCCCG others(121): Show |
C | 2 | a0001c0001t0084g0258a0001c0001t0085g0263 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.793+2226_793+2353d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577810 | |||||
chr18:49577837 | T | C | 1 | a0001c0001t0076g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.793+2247T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577837 | ||||||
chr18:49577837 | T | TG | 16 | a0001c0001t0002g0097a0001c0001t0002g0117a0001c0001t0002g0260others(13): Show | 16 | HG00140.hp2 HG00544.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.793+2254dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577837 | |||||
chr18:49577838 | G | A | 1 | a0001c0001t0076g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.793+2248G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577838 | ||||||
chr18:49577838 | G | C | 1 | a0002c0002t0005g0348 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793+2248G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577838 | ||||||
chr18:49577848 | A | AC | 12 | a0001c0001t0001g0246a0001c0001t0002g0032a0001c0001t0002g0260others(9): Show | 12 | HG01099.hp2 HG01175.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.793+2265dupC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577848 | |||||
chr18:49577906 | C | T | 2 | a0002c0002t0005g0346a0002c0002t0005g0365 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793+2316C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577906 | ||||||
chr18:49577908 | AGTAGGGG others(228): Show |
A | 2 | a0002c0002t0005g0346a0002c0002t0005g0365 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793+2320_793+2554d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577908 | |||||
chr18:49577916 | T | C | 137 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.793+2326T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577916 | ||||||
chr18:49577949 | G | C | 59 | a0001c0001t0003g0041a0001c0001t0006g0034a0001c0001t0006g0037others(56): Show | 60 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.793+2359G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577949 | ||||||
chr18:49577954 | G | A | 64 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(61): Show | 65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.793+2364G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577954 | ||||||
chr18:49577961 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2371C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577961 | ||||||
chr18:49577975 | AC | A | 12 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.793+2392delC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577975 | |||||
chr18:49577976 | C | T | 16 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(13): Show | 16 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+2386C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577976 | ||||||
chr18:49577982 | C | A | 3 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0049g0292 | 3 | HG01891.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.793+2392C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577982 | ||||||
chr18:49577991 | C | T | 16 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(13): Show | 16 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+2401C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577991 | ||||||
chr18:49578003 | G | T | 1 | a0001c0001t0044g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793+2413G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578003 | ||||||
chr18:49578051 | C | T | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+2461C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578051 | ||||||
chr18:49578063 | C | CG | 11 | a0001c0001t0001g0246a0001c0001t0002g0115a0001c0001t0003g0121others(8): Show | 11 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+2480dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578063 | |||||
chr18:49578063 | C | T | 1 | a0001c0001t0056g0296 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.793+2473C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578063 | ||||||
chr18:49578069 | G | T | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+2479G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578069 | ||||||
chr18:49578074 | G | A | 6 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0049g0292others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+2484G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578074 | ||||||
chr18:49578109 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2519G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578109 | ||||||
chr18:49578112 | C | CG | 10 | a0001c0001t0001g0212a0001c0001t0001g0246a0001c0001t0001g0284others(7): Show | 10 | HG00140.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+2528dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578112 | |||||
chr18:49578122 | AC | A | 265 | a0001c0001t0001g0052a0001c0001t0001g0206a0001c0001t0001g0208others(262): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.793+2541delC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578122 | |||||
chr18:49578146 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.793+2556C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578146 | ||||||
chr18:49578163 | G | A | 1 | a0002c0002t0054g0344 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793+2573G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578163 | ||||||
chr18:49578168 | C | T | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+2578C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578168 | ||||||
chr18:49578174 | T | G | 1 | a0001c0003t0045g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.793+2584T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578174 | ||||||
chr18:49578178 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2588C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578178 | ||||||
chr18:49578245 | A | G | 1 | a0001c0003t0045g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.793+2655A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578245 | ||||||
chr18:49578249 | G | A | 1 | a0001c0001t0126g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.793+2659G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578249 | ||||||
chr18:49578252 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.793+2662C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578252 | ||||||
chr18:49578306 | C | G | 1 | a0001c0001t0044g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.793+2716C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578306 | ||||||
chr18:49578312 | A | G | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2722A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578312 | ||||||
chr18:49578315 | C | CG | 7 | a0001c0001t0001g0052a0001c0001t0002g0119a0001c0001t0002g0261others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.793+2728dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578315 | |||||
chr18:49578325 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2735C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578325 | ||||||
chr18:49578335 | C | G | 1 | a0002c0002t0022g0317 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.793+2745C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578335 | ||||||
chr18:49578343 | C | CG | 5 | a0001c0001t0008g0193a0001c0001t0013g0099a0001c0001t0046g0096others(2): Show | 5 | HG01175.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+2757dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578343 | |||||
chr18:49578343 | C | G | 46 | a0001c0001t0102g0143a0001c0001t0106g0144a0002c0002t0005g0003others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.793+2753C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578343 | ||||||
chr18:49578351 | C | G | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2761C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578351 | ||||||
chr18:49578352 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.793+2762G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578352 | ||||||
chr18:49578366 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2776G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578366 | ||||||
chr18:49578391 | C | CG | 7 | a0001c0001t0001g0246a0001c0001t0003g0126a0001c0001t0003g0139others(4): Show | 7 | HG01516.hp2 HG01978.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.793+2805dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578391 | |||||
chr18:49578403 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2813G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578403 | ||||||
chr18:49578440 | A | G | 1 | a0001c0001t0011g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.793+2850A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578440 | ||||||
chr18:49578481 | C | T | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+2891C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578481 | ||||||
chr18:49578507 | C | T | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2908C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578507 | ||||||
chr18:49578508 | G | C | 1 | a0001c0001t0095g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.794-2907G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578508 | ||||||
chr18:49578511 | C | T | 1 | a0001c0003t0121g0181 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.794-2904C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578511 | ||||||
chr18:49578512 | G | A | 2 | a0001c0001t0081g0269a0001c0001t0082g0272 | 2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.794-2903G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578512 | ||||||
chr18:49578521 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2894C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578521 | ||||||
chr18:49578592 | G | A | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2823G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578592 | ||||||
chr18:49578615 | T | C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2800T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578615 | ||||||
chr18:49578615 | T | TG | 15 | a0001c0001t0001g0052a0001c0001t0001g0225a0001c0001t0001g0232others(12): Show | 15 | HG01109.hp2 HG01978.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.794-2796dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578615 | |||||
chr18:49578621 | G | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2794G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578621 | ||||||
chr18:49578646 | C | G | 1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794-2769C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578646 | ||||||
chr18:49578684 | T | G | 12 | a0001c0001t0003g0041a0001c0001t0003g0139a0001c0001t0006g0034others(9): Show | 12 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-2731T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578684 | ||||||
chr18:49578698 | C | T | 1 | a0001c0001t0131g0279 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.794-2717C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578698 | ||||||
chr18:49578736 | G | T | 1 | a0003c0004t0016g0167 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.794-2679G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578736 | ||||||
chr18:49578750 | G | C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2665G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578750 | ||||||
chr18:49578825 | G | A | 16 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(13): Show | 16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-2590G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578825 | ||||||
chr18:49578827 | C | T | 1 | a0002c0002t0005g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.794-2588C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578827 | ||||||
chr18:49578828 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.794-2587C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578828 | ||||||
chr18:49578835 | A | T | 1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794-2580A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578835 | ||||||
chr18:49578854 | C | G | 3 | a0002c0002t0004g0302a0002c0002t0018g0173a0002c0002t0130g0171 | 3 | HG02015.hp1 NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.794-2561C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578854 | ||||||
chr18:49578881 | GCGTGCCT others(5): Show |
G | 77 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(74): Show | 78 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.794-2531_794-2520d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578881 | |||||
chr18:49578886 | C | A | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2529C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578886 | ||||||
chr18:49578894 | C | T | 3 | a0001c0001t0049g0292a0001c0001t0097g0267a0001c0001t0098g0268 | 3 | NA18944.hp2 NA19030.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2521C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578894 | ||||||
chr18:49578905 | G | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2510G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578905 | ||||||
chr18:49578974 | T | C | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794-2441T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578974 | ||||||
chr18:49578983 | A | G | 1 | a0001c0001t0135g0220 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.794-2432A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578983 | ||||||
chr18:49579001 | G | GGGGAGA | 4 | a0001c0001t0001g0283a0001c0001t0012g0142a0001c0003t0007g0194others(1): Show | 4 | HG01106.hp1 HG01106.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2182_794-2177d others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(33): Show |
1 | a0001c0001t0003g0041 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(41): Show |
1 | a0001c0001t0115g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(17): Show |
1 | a0001c0001t0006g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(41): Show |
1 | a0001c0001t0044g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(143): Show |
1 | a0001c0001t0006g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(152): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(17): Show |
1 | a0001c0001t0006g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(41): Show |
2 | a0001c0001t0006g0034a0001c0001t0006g0042 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.794-2408_794-2407i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(59): Show |
1 | a0001c0001t0129g0138 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(68): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAC others(54): Show |
1 | a0001c0001t0032g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(63): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(51): Show |
1 | a0001c0001t0001g0175 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.794-2407_794-2406i others(60): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(124): Show |
1 | a0002c0002t0064g0379 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.794-2406_794-2405i others(133): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(5): Show |
7 | a0001c0001t0001g0215a0001c0001t0002g0108a0001c0001t0002g0117others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2188_794-2177d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(35): Show |
1 | a0002c0002t0004g0300 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.794-2402_794-2401i others(44): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(53): Show |
1 | a0002c0002t0009g0360 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.794-2400_794-2399i others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(11): Show |
5 | a0001c0001t0001g0282a0001c0001t0010g0151a0001c0001t0012g0088others(2): Show | 5 | HG01070.hp1 HG02602.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2194_794-2177d others(20): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(17): Show |
8 | a0001c0001t0002g0097a0001c0001t0002g0107a0001c0001t0003g0016others(5): Show | 8 | HG00544.hp1 HG00609.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2200_794-2177d others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(41): Show |
1 | a0001c0001t0019g0231 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.794-2386_794-2385i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(23): Show |
5 | a0001c0001t0003g0125a0001c0001t0039g0178a0001c0001t0047g0207others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2206_794-2177d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(29): Show |
13 | a0001c0001t0001g0245a0001c0001t0002g0032a0001c0001t0002g0119others(10): Show | 13 | HG01099.hp2 HG01358.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.794-2212_794-2177d others(38): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(35): Show |
18 | a0001c0001t0001g0211a0001c0001t0001g0227a0001c0001t0001g0236others(15): Show | 18 | HG01168.hp2 HG01258.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-2218_794-2177d others(44): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(41): Show |
16 | a0001c0001t0002g0134a0001c0001t0003g0010a0001c0001t0003g0011others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-2224_794-2177d others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(46): Show |
1 | a0001c0001t0013g0057 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.794-2364_794-2363i others(55): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(82): Show |
1 | a0002c0002t0014g0332 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.794-2364_794-2363i others(91): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(47): Show |
13 | a0001c0001t0001g0223a0001c0001t0001g0243a0001c0001t0001g0244others(10): Show | 13 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-2230_794-2177d others(56): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(53): Show |
12 | a0001c0001t0001g0224a0001c0001t0002g0129a0001c0001t0008g0197others(9): Show | 13 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-2236_794-2177d others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(59): Show |
17 | a0001c0001t0001g0218a0001c0001t0001g0235a0001c0001t0001g0284others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.794-2242_794-2177d others(68): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(65): Show |
21 | a0001c0001t0001g0213a0001c0001t0001g0222a0001c0001t0001g0232others(18): Show | 21 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.794-2248_794-2177d others(74): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(71): Show |
13 | a0001c0001t0002g0094a0001c0001t0002g0115a0001c0001t0002g0128others(10): Show | 13 | HG00423.hp2 HG02056.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-2254_794-2177d others(80): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(77): Show |
17 | a0001c0001t0002g0054a0001c0001t0002g0080a0001c0001t0002g0118others(14): Show | 17 | HG00741.hp2 HG01069.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.794-2260_794-2177d others(86): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(82): Show |
1 | a0002c0002t0005g0340 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.794-2328_794-2327i others(91): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(83): Show |
9 | a0001c0001t0001g0233a0001c0001t0003g0262a0001c0001t0012g0069others(6): Show | 9 | HG00140.hp2 HG02165.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-2266_794-2177d others(92): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(89): Show |
10 | a0001c0001t0001g0214a0001c0001t0001g0241a0001c0001t0002g0033others(7): Show | 11 | HG01496.hp2 HG01943.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-2272_794-2177d others(98): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(95): Show |
8 | a0001c0001t0006g0078a0001c0001t0006g0079a0001c0001t0011g0062others(5): Show | 8 | HG00558.hp1 HG01496.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-2278_794-2177d others(104): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(101): Show |
5 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0037g0077others(2): Show | 6 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2284_794-2177d others(110): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(107): Show |
6 | a0001c0001t0010g0149a0001c0001t0011g0065a0001c0001t0015g0028others(3): Show | 6 | HG00642.hp1 HG01433.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-2290_794-2177d others(116): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(113): Show |
9 | a0001c0001t0001g0206a0001c0001t0003g0018a0001c0001t0010g0158others(6): Show | 9 | HG00280.hp1 HG01358.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.794-2296_794-2177d others(122): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(119): Show |
3 | a0001c0001t0002g0105a0001c0001t0019g0248a0001c0001t0140g0104 | 3 | HG00438.hp2 HG00738.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.794-2302_794-2177d others(128): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(125): Show |
4 | a0001c0001t0003g0093a0001c0001t0019g0219a0001c0001t0137g0100others(1): Show | 4 | HG02300.hp1 NA18612.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2308_794-2177d others(134): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(131): Show |
3 | a0002c0002t0004g0319a0002c0002t0022g0305a0002c0002t0069g0331 | 3 | HG02155.hp2 NA18939.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.794-2314_794-2177d others(140): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(137): Show |
2 | a0001c0001t0002g0074a0002c0002t0021g0378 | 2 | HG01167.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.794-2320_794-2177d others(146): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(149): Show |
2 | a0001c0001t0011g0066a0002c0002t0059g0352 | 2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.794-2332_794-2177d others(158): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(155): Show |
1 | a0002c0002t0005g0353 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.794-2338_794-2177d others(164): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(167): Show |
1 | a0002c0002t0004g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.794-2350_794-2177d others(176): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(24): Show |
1 | a0001c0001t0002g0095 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794-2393_794-2392i others(33): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGAGAG others(78): Show |
1 | a0001c0001t0107g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.794-2393_794-2392i others(87): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | G | GGGGGGAG others(35): Show |
1 | a0002c0002t0030g0322 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.794-2411_794-2410i others(44): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(5): Show |
G | 4 | a0001c0001t0003g0015a0001c0001t0039g0189a0002c0002t0005g0346others(1): Show | 4 | HG01071.hp1 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2188_794-2177d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(11): Show |
G | 2 | a0001c0001t0061g0036a0002c0002t0005g0365 | 2 | HG01070.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.794-2194_794-2177d others(20): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(17): Show |
G | 1 | a0002c0002t0014g0336 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.794-2200_794-2177d others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(23): Show |
G | 2 | a0001c0001t0055g0326a0001c0003t0007g0199 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.794-2206_794-2177d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(29): Show |
G | 1 | a0001c0005t0007g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.794-2212_794-2177d others(38): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(41): Show |
G | 1 | a0001c0001t0011g0064 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.794-2224_794-2177d others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(53): Show |
G | 1 | a0001c0003t0007g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.794-2236_794-2177d others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(59): Show |
G | 1 | a0002c0002t0063g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2242_794-2177d others(68): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(65): Show |
G | 2 | a0001c0001t0001g0225a0001c0001t0015g0027 | 2 | HG01981.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.794-2248_794-2177d others(74): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(71): Show |
G | 2 | a0001c0001t0001g0237a0001c0001t0020g0375 | 2 | HG00733.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2254_794-2177d others(80): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(77): Show |
G | 1 | a0001c0001t0084g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2260_794-2177d others(86): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(95): Show |
G | 2 | a0001c0001t0003g0017a0001c0003t0121g0181 | 2 | HG03017.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.794-2278_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(113): Show |
G | 1 | a0001c0001t0052g0374 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.794-2296_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(137): Show |
G | 2 | a0001c0001t0002g0256a0001c0001t0112g0020 | 2 | HG01081.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.794-2320_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(143): Show |
G | 1 | a0001c0001t0027g0205 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.794-2326_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(155): Show |
G | 1 | a0001c0001t0001g0208 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.794-2338_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(161): Show |
G | 2 | a0001c0001t0001g0209a0001c0001t0001g0212 | 2 | HG02004.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.794-2344_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(167): Show |
G | 1 | a0002c0002t0062g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.794-2350_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(173): Show |
G | 2 | a0001c0001t0077g0031a0001c0001t0095g0026 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.794-2356_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(179): Show |
G | 3 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0096g0029 | 3 | HG02071.hp1 HG02965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.794-2362_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579001 | GGGGAGAG others(185): Show |
G | 4 | a0001c0001t0001g0210a0001c0001t0094g0030a0001c0001t0097g0267others(1): Show | 4 | HG02622.hp2 NA18944.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2368_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | |||||
chr18:49579002 | G | GGGAGACG others(5): Show |
1 | a0001c0001t0128g0040 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579002 | |||||
chr18:49579003 | G | GGAGAGGG others(3): Show |
1 | a0002c0002t0009g0361 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.794-2410_794-2401d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579003 | |||||
chr18:49579004 | G | GAGAGGTA others(221): Show |
2 | a0001c0001t0001g0092a0002c0002t0050g0323 | 2 | NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.794-2406_794-2405i others(230): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579004 | |||||
chr18:49579004 | G | GGGAGAGG others(187): Show |
1 | a0001c0001t0037g0136 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.794-2411_794-2410i others(196): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579004 | ||||||
chr18:49579007 | A | G | 1 | a0001c0003t0045g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.794-2408A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579007 | ||||||
chr18:49579007 | AGGGAGAG others(34): Show |
A | 1 | a0001c0001t0032g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.794-2407_794-2367d others(43): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579007 | ||||||
chr18:49579008 | G | C | 1 | a0001c0001t0128g0040 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.794-2407G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579008 | ||||||
chr18:49579008 | GGGAGAGG others(106): Show |
G | 1 | a0001c0001t0034g0101 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.794-2404_794-2292d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579008 | |||||
chr18:49579008 | GGGAGAGG others(190): Show |
G | 2 | a0001c0001t0104g0163a0001c0001t0105g0162 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.794-2404_794-2208d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579008 | |||||
chr18:49579008 | GGGAGAGG others(196): Show |
G | 3 | a0001c0001t0041g0160a0001c0001t0110g0164a0001c0001t0117g0161 | 3 | HG02970.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794-2404_794-2202d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579008 | |||||
chr18:49579009 | G | GAGAGGGA others(30): Show |
1 | a0001c0001t0001g0052 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.794-2406_794-2405i others(39): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579009 | ||||||
chr18:49579009 | G | GGAGAGGG others(19): Show |
1 | a0001c0001t0018g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.794-2402_794-2377d others(28): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579009 | |||||
chr18:49579010 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2405G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579010 | ||||||
chr18:49579011 | A | C | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.794-2404A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579011 | ||||||
chr18:49579011 | A | G | 2 | a0002c0002t0022g0321a0002c0002t0030g0315 | 2 | NA18998.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.794-2404A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579011 | ||||||
chr18:49579013 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2399dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579013 | |||||
chr18:49579014 | G | C | 3 | a0001c0001t0128g0040a0004c0006t0087g0170a0004c0006t0088g0169 | 3 | HG01346.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-2401G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579014 | ||||||
chr18:49579015 | G | C | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-2400G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579015 | ||||||
chr18:49579015 | G | T | 1 | a0001c0001t0002g0111 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.794-2400G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579015 | ||||||
chr18:49579016 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2399G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579016 | ||||||
chr18:49579017 | A | AGAGGGAG others(31): Show |
1 | a0001c0001t0048g0271 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.794-2391_794-2390i others(40): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579017 | |||||
chr18:49579017 | A | G | 16 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(13): Show | 16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-2398A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579017 | ||||||
chr18:49579017 | A | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-2398A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579017 | ||||||
chr18:49579018 | GAGGGAGA others(30): Show |
G | 1 | a0004c0006t0088g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.794-2396_794-2360d others(39): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579018 | ||||||
chr18:49579018 | GAGGGAGA others(36): Show |
G | 1 | a0004c0006t0087g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.794-2396_794-2354d others(45): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579018 | ||||||
chr18:49579019 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(1): Show | 4 | HG01257.hp1 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2393dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579019 | |||||
chr18:49579019 | A | G | 1 | a0001c0001t0053g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2396A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579019 | ||||||
chr18:49579020 | G | C | 1 | a0001c0001t0128g0040 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.794-2395G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579020 | ||||||
chr18:49579020 | G | GGGAGAGG others(46): Show |
1 | a0001c0001t0003g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.794-2392_794-2340d others(55): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579020 | |||||
chr18:49579020 | G | GGGAGAGG others(118): Show |
1 | a0001c0001t0003g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.794-2392_794-2268d others(127): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579020 | |||||
chr18:49579021 | GGAGAGGG others(93): Show |
G | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.794-2392_794-2293d others(102): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579021 | |||||
chr18:49579021 | GGAGAGGG others(163): Show |
G | 1 | a0001c0001t0024g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.794-2390_794-2221d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579021 | |||||
chr18:49579021 | GGAGAGGG others(169): Show |
G | 1 | a0001c0001t0076g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.794-2390_794-2215d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579021 | |||||
chr18:49579022 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2393G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579022 | ||||||
chr18:49579023 | A | G | 14 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.794-2392A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579023 | ||||||
chr18:49579025 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(1): Show | 4 | HG01257.hp1 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2387dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579025 | |||||
chr18:49579025 | A | G | 2 | a0001c0001t0003g0013a0001c0001t0053g0338 | 2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.794-2390A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579025 | ||||||
chr18:49579027 | G | A | 1 | a0001c0001t0035g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2388G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579027 | ||||||
chr18:49579027 | GGAGAGGG others(147): Show |
G | 2 | a0001c0001t0033g0276a0001c0001t0083g0274 | 2 | HG00738.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.794-2386_794-2233d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | |||||
chr18:49579027 | GGAGAGGG others(151): Show |
G | 1 | a0001c0001t0024g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.794-2384_794-2227d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | |||||
chr18:49579027 | GGAGAGGG others(153): Show |
G | 2 | a0001c0001t0033g0275a0001c0001t0086g0273 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.794-2386_794-2227d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | |||||
chr18:49579027 | GGAGAGGG others(163): Show |
G | 1 | a0001c0001t0024g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.794-2384_794-2215d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | |||||
chr18:49579028 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2387G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579028 | ||||||
chr18:49579029 | A | G | 14 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.794-2386A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579029 | ||||||
chr18:49579031 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2381dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579031 | |||||
chr18:49579031 | A | G | 2 | a0001c0001t0003g0013a0001c0001t0053g0338 | 2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.794-2384A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579031 | ||||||
chr18:49579033 | GGAGAGGG others(9): Show |
G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2380_794-2365d others(18): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579033 | |||||
chr18:49579034 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2381G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579034 | ||||||
chr18:49579034 | GAGAGGGA others(170): Show |
G | 1 | a0004c0006t0029g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.794-2380_794-2204d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579034 | ||||||
chr18:49579035 | A | G | 14 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.794-2380A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579035 | ||||||
chr18:49579037 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2375dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579037 | |||||
chr18:49579037 | A | G | 1 | a0001c0001t0053g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2378A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579037 | ||||||
chr18:49579038 | GGGAGAGG others(154): Show |
G | 5 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2374_794-2214d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579038 | |||||
chr18:49579040 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2375G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579040 | ||||||
chr18:49579040 | GAGAGGGA others(152): Show |
G | 1 | a0004c0006t0029g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.794-2374_794-2216d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579040 | ||||||
chr18:49579041 | A | G | 9 | a0001c0001t0003g0013a0001c0001t0017g0290a0003c0004t0016g0145others(6): Show | 9 | HG00733.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.794-2374A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579041 | ||||||
chr18:49579043 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2369dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579043 | |||||
chr18:49579043 | A | G | 1 | a0001c0001t0053g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2372A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579043 | ||||||
chr18:49579044 | G | GGGAGAGG others(22): Show |
1 | a0001c0001t0012g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.794-2368_794-2340d others(31): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579044 | |||||
chr18:49579044 | GGGAGAGG others(148): Show |
G | 1 | a0001c0001t0017g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.794-2368_794-2214d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579044 | |||||
chr18:49579045 | G | A | 1 | a0001c0001t0035g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2370G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579045 | ||||||
chr18:49579045 | G | GAGAGGGA others(105): Show |
1 | a0008c0009t0013g0120 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.794-2370_794-2369i others(114): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579045 | ||||||
chr18:49579046 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2369G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579046 | ||||||
chr18:49579046 | GAGAGGGA others(170): Show |
G | 1 | a0004c0006t0075g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.794-2368_794-2192d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579046 | ||||||
chr18:49579047 | A | G | 8 | a0001c0001t0003g0013a0003c0004t0016g0145a0003c0004t0016g0146others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2368A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579047 | ||||||
chr18:49579049 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2363dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579049 | |||||
chr18:49579049 | A | AGGGAGAG others(48): Show |
1 | a0002c0002t0073g0372 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.794-2363_794-2309d others(57): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579049 | |||||
chr18:49579049 | A | C | 1 | a0001c0001t0032g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.794-2366A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579049 | ||||||
chr18:49579050 | G | GGGAGAGG others(10): Show |
1 | a0001c0001t0019g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.794-2362_794-2346d others(19): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579050 | |||||
chr18:49579050 | GGGAGAGG others(142): Show |
G | 6 | a0003c0004t0016g0145a0003c0004t0016g0146a0003c0004t0016g0148others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2362_794-2214d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579050 | |||||
chr18:49579052 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2363G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579052 | ||||||
chr18:49579052 | GAGAGGGA others(128): Show |
G | 1 | a0001c0001t0003g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.794-2362_794-2228d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579052 | ||||||
chr18:49579053 | A | G | 1 | a0001c0001t0053g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2362A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579053 | ||||||
chr18:49579055 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2357dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579055 | |||||
chr18:49579055 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2360A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579055 | ||||||
chr18:49579058 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2357G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579058 | ||||||
chr18:49579058 | GAGAGGGA others(134): Show |
G | 1 | a0001c0001t0053g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2356_794-2216d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579058 | ||||||
chr18:49579061 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2351dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579061 | |||||
chr18:49579061 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2354A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579061 | ||||||
chr18:49579063 | G | A | 1 | a0001c0001t0035g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2352G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579063 | ||||||
chr18:49579064 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2351G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579064 | ||||||
chr18:49579067 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2345dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579067 | |||||
chr18:49579067 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2348A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579067 | ||||||
chr18:49579070 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2345G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579070 | ||||||
chr18:49579073 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2339dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579073 | |||||
chr18:49579073 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2342A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579073 | ||||||
chr18:49579076 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2339G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579076 | ||||||
chr18:49579079 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2333dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579079 | |||||
chr18:49579079 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2336A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579079 | ||||||
chr18:49579080 | G | C | 1 | a0002c0002t0063g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2335G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579080 | ||||||
chr18:49579080 | G | GGAGAGGA others(31): Show |
1 | a0002c0013t0004g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.794-2334_794-2333i others(40): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579080 | |||||
chr18:49579081 | G | A | 1 | a0001c0001t0035g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2334G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579081 | ||||||
chr18:49579082 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2333G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579082 | ||||||
chr18:49579083 | A | C | 1 | a0001c0001t0015g0027 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.794-2332A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579083 | ||||||
chr18:49579085 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2327dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579085 | |||||
chr18:49579085 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2330A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579085 | ||||||
chr18:49579086 | G | C | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2329G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579086 | ||||||
chr18:49579088 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2327G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579088 | ||||||
chr18:49579089 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2326A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579089 | ||||||
chr18:49579091 | A | AG | 6 | a0001c0001t0001g0052a0001c0001t0002g0091a0001c0001t0002g0110others(3): Show | 6 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2321dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579091 | |||||
chr18:49579091 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2324A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579091 | ||||||
chr18:49579092 | G | C | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2323G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579092 | ||||||
chr18:49579094 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2321G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579094 | ||||||
chr18:49579095 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2320A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579095 | ||||||
chr18:49579097 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2315dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579097 | |||||
chr18:49579097 | A | AGGGAGAG others(33): Show |
1 | a0001c0001t0043g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.794-2310_794-2309i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579097 | |||||
chr18:49579097 | A | G | 2 | a0001c0001t0001g0225a0001c0001t0012g0123 | 2 | HG01168.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.794-2318A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579097 | ||||||
chr18:49579098 | G | C | 2 | a0001c0001t0011g0064a0001c0001t0020g0375 | 2 | HG00733.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.794-2317G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579098 | ||||||
chr18:49579099 | G | A | 1 | a0001c0001t0035g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2316G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579099 | ||||||
chr18:49579100 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2315G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579100 | ||||||
chr18:49579101 | A | AGAGGGAG others(96): Show |
1 | a0002c0002t0071g0362 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.794-2286_794-2285i others(105): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579101 | |||||
chr18:49579101 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2314A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579101 | ||||||
chr18:49579101 | A | G | 1 | a0002c0013t0004g0328 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.794-2314A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579101 | ||||||
chr18:49579103 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2309dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579103 | |||||
chr18:49579103 | A | G | 2 | a0001c0001t0001g0237a0001c0001t0012g0123 | 2 | HG01168.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2312A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579103 | ||||||
chr18:49579104 | G | C | 2 | a0001c0001t0011g0064a0001c0001t0020g0375 | 2 | HG00733.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.794-2311G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579104 | ||||||
chr18:49579106 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2309G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579106 | ||||||
chr18:49579107 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2308A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579107 | ||||||
chr18:49579109 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(1): Show | 4 | HG01981.hp2 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2303dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579109 | |||||
chr18:49579109 | A | G | 2 | a0001c0001t0001g0225a0001c0001t0012g0123 | 2 | HG01168.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.794-2306A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579109 | ||||||
chr18:49579110 | G | C | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2305G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579110 | ||||||
chr18:49579112 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2303G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579112 | ||||||
chr18:49579112 | GAGA | G | 3 | a0001c0001t0035g0116a0001c0001t0090g0109a0003c0004t0109g0204 | 3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2302_794-2300d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579112 | ||||||
chr18:49579113 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2302A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579113 | ||||||
chr18:49579115 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(1): Show | 4 | HG01981.hp2 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2297dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579115 | |||||
chr18:49579115 | A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0012g0123 | 3 | HG01168.hp1 NA19067.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2300A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579115 | ||||||
chr18:49579116 | G | GGGAGAGG others(63): Show |
1 | a0001c0001t0001g0280 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.794-2232_794-2231i others(72): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579116 | |||||
chr18:49579117 | G | A | 3 | a0001c0001t0035g0116a0001c0001t0090g0109a0003c0004t0109g0204 | 3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2298G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579117 | ||||||
chr18:49579118 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2297G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579118 | ||||||
chr18:49579119 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2296A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579119 | ||||||
chr18:49579119 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2296A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579119 | ||||||
chr18:49579119 | A | T | 1 | a0001c0001t0084g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2296A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579119 | ||||||
chr18:49579120 | GA | G | 3 | a0001c0001t0035g0116a0001c0001t0090g0109a0003c0004t0109g0204 | 3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2294delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579120 | ||||||
chr18:49579121 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(1): Show | 4 | HG01981.hp2 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2291dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579121 | |||||
chr18:49579121 | A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0012g0123 | 3 | HG01168.hp1 NA19067.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2294A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579121 | ||||||
chr18:49579122 | G | GGGAGAGG others(4): Show |
1 | a0001c0001t0002g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.794-2290_794-2280d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579122 | |||||
chr18:49579124 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2291G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579124 | ||||||
chr18:49579125 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2290A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579125 | ||||||
chr18:49579125 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2290A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579125 | ||||||
chr18:49579125 | A | T | 1 | a0001c0001t0084g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2290A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579125 | ||||||
chr18:49579127 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2285dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579127 | |||||
chr18:49579127 | A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0001g0246others(2): Show | 5 | HG01168.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2288A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579127 | ||||||
chr18:49579130 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2285G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579130 | ||||||
chr18:49579130 | GAGA | G | 3 | a0001c0001t0035g0116a0001c0001t0090g0109a0003c0004t0109g0204 | 3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2284_794-2282d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579130 | ||||||
chr18:49579131 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2284A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579131 | ||||||
chr18:49579131 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2284A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579131 | ||||||
chr18:49579133 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(2): Show | 5 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2279dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579133 | |||||
chr18:49579133 | A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0001g0246others(2): Show | 5 | HG01168.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2282A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579133 | ||||||
chr18:49579135 | G | A | 3 | a0001c0001t0035g0116a0001c0001t0090g0109a0003c0004t0109g0204 | 3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2280G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579135 | ||||||
chr18:49579136 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2279G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579136 | ||||||
chr18:49579137 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2278A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579137 | ||||||
chr18:49579137 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2278A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579137 | ||||||
chr18:49579138 | GA | G | 3 | a0001c0001t0035g0116a0001c0001t0090g0109a0003c0004t0109g0204 | 3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2276delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579138 | ||||||
chr18:49579139 | A | AG | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2273dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579139 | |||||
chr18:49579139 | A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0001g0246others(2): Show | 5 | HG01168.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2276A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579139 | ||||||
chr18:49579142 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2273G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579142 | ||||||
chr18:49579143 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2272A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579143 | ||||||
chr18:49579143 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2272A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579143 | ||||||
chr18:49579145 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2267dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579145 | |||||
chr18:49579145 | A | G | 4 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2270A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579145 | ||||||
chr18:49579146 | G | GGGAGAGG others(111): Show |
1 | a0001c0001t0001g0251 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.794-2250_794-2249i others(120): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579146 | |||||
chr18:49579148 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2267G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579148 | ||||||
chr18:49579148 | GAGA | G | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2266_794-2264d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579148 | ||||||
chr18:49579149 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2266A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579149 | ||||||
chr18:49579149 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2266A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579149 | ||||||
chr18:49579151 | A | AG | 5 | a0001c0001t0001g0052a0001c0001t0002g0091a0001c0001t0002g0110others(2): Show | 5 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2261dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579151 | |||||
chr18:49579151 | A | G | 4 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2264A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579151 | ||||||
chr18:49579153 | G | A | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2262G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579153 | ||||||
chr18:49579154 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2261G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579154 | ||||||
chr18:49579155 | A | AGAGGGAG others(99): Show |
1 | a0002c0002t0067g0327 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(108): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579155 | |||||
chr18:49579155 | A | C | 2 | a0001c0001t0015g0027a0002c0002t0063g0304 | 2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2260A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579155 | ||||||
chr18:49579155 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2260A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579155 | ||||||
chr18:49579156 | GA | G | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2258delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579156 | ||||||
chr18:49579157 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2255dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579157 | |||||
chr18:49579157 | A | G | 4 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2258A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579157 | ||||||
chr18:49579160 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2255G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579160 | ||||||
chr18:49579161 | A | C | 1 | a0002c0002t0063g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2254A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579161 | ||||||
chr18:49579161 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2254A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579161 | ||||||
chr18:49579163 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2249dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579163 | |||||
chr18:49579163 | A | G | 4 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2252A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579163 | ||||||
chr18:49579166 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2249G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579166 | ||||||
chr18:49579166 | GAGA | G | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2248_794-2246d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579166 | ||||||
chr18:49579167 | A | C | 1 | a0002c0002t0063g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2248A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579167 | ||||||
chr18:49579167 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2248A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579167 | ||||||
chr18:49579169 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2243dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579169 | |||||
chr18:49579169 | A | G | 5 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(2): Show | 5 | HG00741.hp1 HG01081.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2246A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579169 | ||||||
chr18:49579171 | G | A | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2244G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579171 | ||||||
chr18:49579172 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2243G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579172 | ||||||
chr18:49579173 | A | C | 1 | a0002c0002t0063g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2242A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579173 | ||||||
chr18:49579173 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2242A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579173 | ||||||
chr18:49579174 | GA | G | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2240delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579174 | ||||||
chr18:49579175 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2237dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579175 | |||||
chr18:49579175 | A | G | 4 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0052g0374others(1): Show | 4 | HG00741.hp1 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2240A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579175 | ||||||
chr18:49579178 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2237G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579178 | ||||||
chr18:49579179 | A | C | 1 | a0002c0002t0063g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2236A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579179 | ||||||
chr18:49579179 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2236A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579179 | ||||||
chr18:49579181 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2231dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579181 | |||||
chr18:49579181 | A | G | 5 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(2): Show | 5 | HG00741.hp1 HG01081.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2234A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579181 | ||||||
chr18:49579184 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2231G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579184 | ||||||
chr18:49579184 | GAGA | G | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2230_794-2228d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579184 | ||||||
chr18:49579185 | A | G | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2230A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579185 | ||||||
chr18:49579187 | A | AG | 4 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(1): Show | 4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2225dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579187 | |||||
chr18:49579187 | A | G | 7 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0012g0123others(4): Show | 7 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-2228A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579187 | ||||||
chr18:49579188 | G | GGGAGAGG others(34): Show |
1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.794-2224_794-2184d others(43): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579188 | |||||
chr18:49579189 | G | A | 4 | a0001c0001t0034g0090a0001c0001t0035g0116a0001c0001t0090g0109others(1): Show | 4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2226G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579189 | ||||||
chr18:49579190 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2225G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579190 | ||||||
chr18:49579191 | A | G | 2 | a0001c0001t0020g0375a0001c0001t0024g0047 | 2 | HG00733.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.794-2224A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579191 | ||||||
chr18:49579192 | GA | G | 5 | a0001c0001t0003g0013a0001c0001t0034g0090a0001c0001t0035g0116others(2): Show | 5 | HG00733.hp2 HG01257.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2222delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579192 | ||||||
chr18:49579193 | A | AG | 5 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0101others(2): Show | 5 | HG01243.hp2 HG01261.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2219dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579193 | |||||
chr18:49579193 | A | G | 8 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0033g0275others(5): Show | 8 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-2222A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579193 | ||||||
chr18:49579196 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2219G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579196 | ||||||
chr18:49579197 | A | G | 5 | a0001c0001t0003g0013a0001c0001t0020g0375a0001c0001t0024g0047others(2): Show | 5 | HG00733.hp1 HG00733.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2218A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579197 | ||||||
chr18:49579199 | A | G | 8 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0033g0275others(5): Show | 8 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-2216A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579199 | ||||||
chr18:49579200 | G | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2215G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579200 | ||||||
chr18:49579200 | G | GGGAGAGG others(45): Show |
1 | a0001c0001t0025g0254 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.794-2202_794-2201i others(54): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579200 | |||||
chr18:49579202 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2213G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579202 | ||||||
chr18:49579202 | GAGA | G | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2212_794-2210d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579202 | ||||||
chr18:49579203 | A | G | 10 | a0001c0001t0003g0013a0001c0001t0020g0375a0001c0001t0024g0046others(7): Show | 10 | HG00733.hp1 HG00733.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-2212A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579203 | ||||||
chr18:49579205 | A | AGGGAGAG others(66): Show |
1 | a0001c0001t0002g0260 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(75): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579205 | |||||
chr18:49579205 | A | G | 22 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0017g0285others(19): Show | 22 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.794-2210A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579205 | ||||||
chr18:49579206 | G | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2209G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579206 | ||||||
chr18:49579207 | G | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2208G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579207 | ||||||
chr18:49579207 | G | GGAGGAGG others(28): Show |
1 | a0002c0002t0004g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.794-2205_794-2204i others(37): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579207 | |||||
chr18:49579207 | G | GGGAGAGG others(80): Show |
1 | a0001c0001t0035g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.794-2207_794-2206i others(89): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579207 | |||||
chr18:49579208 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2207G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579208 | ||||||
chr18:49579209 | A | G | 11 | a0001c0001t0003g0013a0001c0001t0020g0375a0001c0001t0024g0046others(8): Show | 11 | HG00733.hp1 HG00733.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-2206A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579209 | ||||||
chr18:49579210 | GA | G | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2204delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579210 | ||||||
chr18:49579211 | A | G | 11 | a0001c0001t0001g0246a0001c0001t0003g0017a0001c0001t0033g0275others(8): Show | 11 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.794-2204A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579211 | ||||||
chr18:49579214 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2201G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579214 | ||||||
chr18:49579215 | A | G | 10 | a0001c0001t0020g0375a0001c0001t0024g0046a0001c0001t0024g0047others(7): Show | 10 | HG00733.hp1 HG02071.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.794-2200A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579215 | ||||||
chr18:49579217 | A | AG | 7 | a0001c0001t0034g0101a0001c0001t0035g0113a0001c0001t0041g0160others(4): Show | 7 | HG01261.hp2 HG01981.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2195dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579217 | |||||
chr18:49579217 | A | G | 6 | a0001c0001t0003g0017a0001c0001t0052g0374a0001c0001t0053g0338others(3): Show | 6 | HG00741.hp1 HG01081.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-2198A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579217 | ||||||
chr18:49579218 | G | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2197G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579218 | ||||||
chr18:49579218 | G | GGGAGAGG others(34): Show |
1 | a0001c0001t0102g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(43): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579218 | |||||
chr18:49579220 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2195G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579220 | ||||||
chr18:49579220 | GAGA | G | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2194_794-2192d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579220 | ||||||
chr18:49579221 | A | G | 10 | a0001c0001t0020g0375a0001c0001t0024g0046a0001c0001t0024g0047others(7): Show | 10 | HG00733.hp1 HG02071.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.794-2194A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579221 | ||||||
chr18:49579223 | A | AG | 8 | a0001c0001t0034g0101a0001c0001t0035g0113a0001c0001t0041g0160others(5): Show | 8 | HG01261.hp2 HG01981.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2189dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579223 | |||||
chr18:49579223 | A | G | 7 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0052g0374others(4): Show | 7 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-2192A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579223 | ||||||
chr18:49579224 | G | C | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2191G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579224 | ||||||
chr18:49579224 | G | GGGAGAGG others(86): Show |
1 | a0001c0001t0002g0081 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(95): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579224 | |||||
chr18:49579225 | G | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2190G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579225 | ||||||
chr18:49579226 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2189G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579226 | ||||||
chr18:49579227 | A | G | 9 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(6): Show | 9 | HG02071.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-2188A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579227 | ||||||
chr18:49579228 | G | C | 1 | a0001c0001t0002g0111 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.794-2187G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579228 | ||||||
chr18:49579228 | GA | G | 6 | a0001c0001t0002g0091a0001c0001t0002g0110a0001c0001t0034g0090others(3): Show | 6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2186delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579228 | ||||||
chr18:49579229 | A | AG | 8 | a0001c0001t0034g0101a0001c0001t0035g0113a0001c0001t0041g0160others(5): Show | 8 | HG01261.hp2 HG01981.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2183dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579229 | |||||
chr18:49579229 | A | G | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2186A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579229 | ||||||
chr18:49579232 | G | T | 3 | a0001c0001t0001g0092a0001c0001t0037g0136a0002c0002t0050g0323 | 3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2183G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579232 | ||||||
chr18:49579233 | A | AGAGGGAG others(54): Show |
1 | a0001c0001t0002g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(63): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579233 | |||||
chr18:49579233 | A | G | 4 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2182A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579233 | ||||||
chr18:49579233 | A | T | 1 | a0001c0001t0084g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2182A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579233 | ||||||
chr18:49579234 | G | C | 3 | a0001c0001t0015g0024a0001c0001t0044g0035a0001c0001t0124g0154 | 3 | HG01192.hp2 HG01891.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.794-2181G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579234 | ||||||
chr18:49579234 | G | GAGGGAGA others(47): Show |
1 | a0001c0001t0015g0023 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(56): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579234 | |||||
chr18:49579234 | G | GAGGGAGA others(119): Show |
1 | a0001c0001t0010g0155 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(128): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579234 | |||||
chr18:49579235 | A | AGGGAGAG others(47): Show |
1 | a0001c0011t0068g0380 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(56): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579235 | |||||
chr18:49579236 | G | GGGAGAGG others(76): Show |
1 | a0001c0001t0001g0229 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(85): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579236 | |||||
chr18:49579239 | C | T | 2 | a0001c0001t0084g0258a0001c0001t0085g0263 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.794-2176C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579239 | ||||||
chr18:49579244 | C | T | 2 | a0001c0001t0001g0211a0001c0001t0047g0207 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.794-2171C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579244 | ||||||
chr18:49579252 | C | T | 1 | a0001c0001t0124g0154 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.794-2163C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579252 | ||||||
chr18:49579358 | T | C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2057T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579358 | ||||||
chr18:49579425 | T | C | 5 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0094g0030others(2): Show | 5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1990T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579425 | ||||||
chr18:49579711 | A | G | 5 | a0001c0001t0008g0184a0001c0001t0008g0192a0001c0001t0008g0196others(2): Show | 5 | HG01928.hp1 HG01975.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1704A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579711 | ||||||
chr18:49579743 | T | C | 4 | a0001c0001t0110g0164a0004c0006t0029g0265a0004c0006t0029g0266others(1): Show | 4 | HG02647.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1672T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579743 | ||||||
chr18:49579743 | T | G | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1672T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579743 | ||||||
chr18:49579743 | T | TCTTTC | 3 | a0001c0001t0003g0061a0001c0001t0010g0158a0005c0010t0010g0255 | 3 | HG03654.hp1 NA19076.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.794-1651_794-1647d others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | |||||
chr18:49579743 | T | TCTTTCCT others(3): Show |
8 | a0001c0001t0006g0008a0001c0001t0006g0039a0001c0001t0006g0043others(5): Show | 8 | HG00639.hp2 HG01243.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-1656_794-1647d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | |||||
chr18:49579743 | T | TCTTTCCT others(8): Show |
6 | a0001c0001t0008g0184a0001c0001t0008g0192a0001c0003t0007g0194others(3): Show | 6 | HG01109.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-1661_794-1647d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | |||||
chr18:49579743 | T | TCTTTCCT others(13): Show |
8 | a0001c0001t0006g0042a0001c0001t0008g0002a0001c0001t0008g0193others(5): Show | 9 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-1666_794-1647d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | |||||
chr18:49579744 | C | CCTTTCCT others(6): Show |
3 | a0001c0001t0104g0163a0001c0001t0105g0162a0001c0001t0117g0161 | 3 | HG02647.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.794-1671_794-1670i others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579744 | ||||||
chr18:49579744 | C | CCTTTCCT others(12): Show |
1 | a0001c0001t0041g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.794-1671_794-1670i others(21): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579744 | ||||||
chr18:49579749 | C | CT | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1663dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579749 | |||||
chr18:49579757 | T | TTC | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1658_794-1657i others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579757 | ||||||
chr18:49579759 | C | T | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1656C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579759 | ||||||
chr18:49579759 | CTTTCCTT others(13): Show |
C | 1 | a0001c0001t0044g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.794-1651_794-1632d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579759 | |||||
chr18:49579759 | CTTTCCTT others(18): Show |
C | 1 | a0001c0001t0049g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.794-1651_794-1627d others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579759 | |||||
chr18:49579759 | CTTTCCTT others(23): Show |
C | 4 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0097g0267others(1): Show | 4 | HG01891.hp2 HG02055.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1651_794-1622d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579759 | |||||
chr18:49579764 | C | CTTTCCTT others(128): Show |
1 | a0007c0007t0026g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(137): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(38): Show |
1 | a0001c0005t0007g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(13): Show |
4 | a0001c0001t0003g0017a0001c0001t0044g0035a0001c0003t0045g0201others(1): Show | 4 | HG01891.hp1 HG02886.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1647_794-1646i others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(18): Show |
6 | a0001c0001t0008g0203a0001c0001t0112g0020a0001c0001t0120g0174others(3): Show | 6 | HG01081.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-1647_794-1646i others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(23): Show |
2 | a0001c0005t0100g0183a0006c0008t0008g0295 | 2 | HG01358.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(28): Show |
5 | a0001c0001t0053g0338a0001c0003t0007g0187a0001c0003t0007g0188others(2): Show | 5 | HG01884.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1647_794-1646i others(37): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(33): Show |
1 | a0001c0001t0052g0374 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(38): Show |
1 | a0001c0001t0107g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(43): Show |
2 | a0001c0001t0119g0294a0001c0005t0007g0182 | 2 | HG00423.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(52): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(53): Show |
2 | a0001c0001t0003g0013a0001c0001t0008g0293 | 2 | HG00544.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(83): Show |
1 | a0001c0001t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(92): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(8): Show |
2 | a0001c0001t0020g0375a0001c0001t0128g0040 | 2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(13): Show |
2 | a0001c0001t0003g0041a0001c0001t0006g0034 | 2 | HG01934.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(18): Show |
2 | a0001c0001t0003g0010a0001c0001t0003g0018 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(23): Show |
2 | a0001c0001t0003g0011a0001c0001t0123g0012 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(28): Show |
2 | a0001c0001t0003g0014a0001c0001t0115g0045 | 2 | HG02622.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(37): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(33): Show |
1 | a0001c0001t0003g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(38): Show |
1 | a0001c0001t0003g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(63): Show |
1 | a0001c0001t0003g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(72): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(3): Show |
2 | a0001c0001t0003g0059a0001c0001t0025g0132 | 2 | NA19009.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(26): Show |
1 | a0001c0001t0040g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(35): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(8): Show |
1 | a0001c0001t0003g0058 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(13): Show |
2 | a0001c0001t0131g0279a0003c0004t0016g0145 | 2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(18): Show |
3 | a0001c0001t0003g0056a0001c0001t0006g0122a0001c0001t0125g0060 | 3 | HG02080.hp1 HG02080.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCCTT others(113): Show |
1 | a0001c0001t0114g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(122): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCT | 26 | a0001c0001t0001g0223a0001c0001t0001g0235a0001c0001t0001g0244others(23): Show | 26 | HG00099.hp1 HG00558.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.794-1598_794-1594d others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCTTT others(3): Show |
20 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0246others(17): Show | 20 | HG01069.hp1 HG01433.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.794-1603_794-1594d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCTTT others(8): Show |
7 | a0001c0001t0002g0081a0001c0001t0002g0091a0001c0001t0002g0110others(4): Show | 7 | HG02074.hp1 HG02572.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-1608_794-1594d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCTTT others(13): Show |
7 | a0001c0001t0006g0079a0001c0001t0013g0106a0001c0001t0013g0131others(4): Show | 7 | HG00609.hp1 HG01361.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-1613_794-1594d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCTTT others(18): Show |
4 | a0001c0001t0011g0067a0001c0001t0013g0099a0001c0001t0013g0102others(1): Show | 4 | HG00741.hp2 HG01978.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1618_794-1594d others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCTTT others(23): Show |
1 | a0003c0004t0016g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794-1623_794-1594d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | C | CTTTCTTT others(53): Show |
2 | a0001c0001t0056g0296a0008c0009t0013g0120 | 2 | HG02293.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.794-1594_794-1593i others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | CTTTCT | C | 36 | a0001c0001t0001g0175a0001c0001t0001g0206a0001c0001t0001g0211others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.794-1598_794-1594d others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | CTTTCTTT others(3): Show |
C | 26 | a0001c0001t0001g0218a0001c0001t0001g0232a0001c0001t0002g0095others(23): Show | 27 | HG00738.hp1 HG01074.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-1603_794-1594d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | CTTTCTTT others(8): Show |
C | 45 | a0001c0001t0001g0052a0001c0001t0001g0213a0001c0001t0001g0214others(42): Show | 45 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.794-1608_794-1594d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | CTTTCTTT others(13): Show |
C | 7 | a0001c0001t0026g0270a0001c0001t0081g0269a0001c0001t0082g0272others(4): Show | 7 | HG01361.hp2 HG01884.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-1613_794-1594d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | CTTTCTTT others(18): Show |
C | 46 | a0001c0001t0001g0092a0001c0001t0102g0143a0001c0001t0106g0144others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.794-1618_794-1594d others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579764 | CTTTCTTT others(23): Show |
C | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794-1623_794-1594d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | |||||
chr18:49579767 | T | TTC | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1648_794-1647i others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579767 | ||||||
chr18:49579768 | CTTTTCTT others(19): Show |
C | 1 | a0002c0002t0009g0355 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.794-1643_794-1618d others(28): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579768 | |||||
chr18:49579769 | T | C | 19 | a0001c0001t0001g0278a0001c0001t0006g0043a0001c0001t0008g0197others(16): Show | 19 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.794-1646T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579769 | ||||||
chr18:49579772 | T | TCCTTTCC others(104): Show |
1 | a0004c0006t0029g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.794-1642_794-1641i others(113): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579772 | |||||
chr18:49579774 | T | C | 19 | a0001c0001t0006g0037a0001c0001t0006g0038a0001c0001t0010g0150others(16): Show | 19 | HG00642.hp1 HG00735.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.794-1641T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579774 | ||||||
chr18:49579777 | T | C | 2 | a0001c0001t0105g0162a0001c0001t0117g0161 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.794-1638T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579777 | ||||||
chr18:49579777 | T | TCCTTTCC others(69): Show |
1 | a0004c0006t0029g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.794-1637_794-1636i others(78): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579777 | |||||
chr18:49579777 | T | TCCTTTCC others(79): Show |
1 | a0004c0006t0075g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.794-1637_794-1636i others(88): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579777 | |||||
chr18:49579777 | T | TTCCTTTT others(26): Show |
1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1638_794-1637i others(35): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579777 | ||||||
chr18:49579778 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.794-1637C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579778 | ||||||
chr18:49579779 | T | C | 5 | a0001c0001t0010g0151a0001c0001t0010g0155a0001c0001t0010g0165others(2): Show | 5 | HG03017.hp2 HG03139.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1636T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579779 | ||||||
chr18:49579781 | TTCTTTTC others(5): Show |
T | 1 | a0002c0002t0004g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.794-1632_794-1621d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579781 | |||||
chr18:49579782 | T | C | 3 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0110g0164 | 3 | HG02647.hp1 HG02970.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794-1633T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579782 | ||||||
chr18:49579784 | T | C | 5 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1631T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579784 | ||||||
chr18:49579787 | T | C | 2 | a0001c0001t0110g0164a0001c0001t0117g0161 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.794-1628T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579787 | ||||||
chr18:49579789 | T | C | 3 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162 | 3 | HG02647.hp1 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.794-1626T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579789 | ||||||
chr18:49579792 | T | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1623T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579792 | ||||||
chr18:49579794 | T | C | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1621T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579794 | ||||||
chr18:49579797 | T | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1618T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579797 | ||||||
chr18:49579799 | T | C | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1616T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579799 | ||||||
chr18:49579802 | T | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1613T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579802 | ||||||
chr18:49579804 | T | C | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1611T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579804 | ||||||
chr18:49579807 | T | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1608T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579807 | ||||||
chr18:49579809 | T | C | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1606T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579809 | ||||||
chr18:49579812 | T | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1603T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579812 | ||||||
chr18:49579814 | T | C | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1601T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579814 | ||||||
chr18:49579817 | T | A | 6 | a0001c0001t0017g0285a0001c0001t0024g0046a0001c0001t0024g0047others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-1598T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579817 | ||||||
chr18:49579817 | T | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1598T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579817 | ||||||
chr18:49579817 | T | TCTTTACT others(3): Show |
1 | a0007c0007t0026g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.794-1593_794-1584d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579817 | |||||
chr18:49579817 | T | TCTTTTCT others(3): Show |
1 | a0001c0001t0003g0262 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.794-1594_794-1593i others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579817 | |||||
chr18:49579817 | T | TCTTTTCT others(8): Show |
4 | a0001c0001t0017g0287a0001c0001t0017g0288a0001c0001t0017g0290others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1594_794-1593i others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579817 | |||||
chr18:49579819 | T | C | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1596T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579819 | ||||||
chr18:49579821 | TAC | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-1593_794-1592d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579821 | ||||||
chr18:49579822 | A | C | 1 | a0001c0001t0110g0164 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1593A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579822 | ||||||
chr18:49579822 | A | T | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1593A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579822 | ||||||
chr18:49579824 | T | C | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1591T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579824 | ||||||
chr18:49579825 | T | C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-1590T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579825 | ||||||
chr18:49579827 | A | T | 4 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1588A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579827 | ||||||
chr18:49579853 | C | T | 2 | a0001c0001t0032g0021a0001c0001t0032g0022 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.794-1562C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579853 | ||||||
chr18:49579880 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-1535C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579880 | ||||||
chr18:49579890 | C | T | 1 | a0002c0002t0004g0370 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.794-1525C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579890 | ||||||
chr18:49579896 | C | T | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1519C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579896 | ||||||
chr18:49579932 | C | G | 1 | a0001c0001t0033g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.794-1483C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579932 | ||||||
chr18:49580040 | C | T | 1 | a0001c0001t0006g0008 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.794-1375C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580040 | ||||||
chr18:49580187 | A | G | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-1228A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580187 | ||||||
chr18:49580230 | A | C | 1 | a0006c0008t0008g0295 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1185A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580230 | ||||||
chr18:49580235 | T | G | 1 | a0006c0008t0008g0295 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1180T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580235 | ||||||
chr18:49580239 | ACCAACTG others(8): Show |
A | 1 | a0006c0008t0008g0295 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1175_794-1161d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580239 | ||||||
chr18:49580255 | A | T | 1 | a0006c0008t0008g0295 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1160A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580255 | ||||||
chr18:49580257 | C | T | 1 | a0001c0001t0134g0217 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.794-1158C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580257 | ||||||
chr18:49580385 | C | T | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-1030C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580385 | ||||||
chr18:49580444 | A | G | 13 | a0001c0001t0055g0326a0001c0001t0107g0190a0001c0003t0007g0187others(10): Show | 13 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-971A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580444 | ||||||
chr18:49580567 | C | T | 4 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-848C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580567 | ||||||
chr18:49580570 | G | A | 6 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0152others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-845G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580570 | ||||||
chr18:49580653 | G | A | 2 | a0002c0002t0004g0301a0002c0002t0004g0320 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.794-762G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580653 | ||||||
chr18:49580658 | GAAAA | G | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-750_794-747del others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49580658 | |||||
chr18:49580772 | G | C | 1 | a0001c0001t0013g0106 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.794-643G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580772 | ||||||
chr18:49580782 | C | G | 95 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(92): Show | 96 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.794-633C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580782 | ||||||
chr18:49580863 | C | T | 42 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.794-552C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580863 | ||||||
chr18:49580918 | T | C | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-497T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580918 | ||||||
chr18:49580980 | C | T | 5 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-435C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580980 | ||||||
chr18:49580981 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.794-434G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580981 | ||||||
chr18:49581081 | A | G | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-334A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581081 | ||||||
chr18:49581084 | C | A | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-331C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581084 | ||||||
chr18:49581284 | A | G | 12 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.794-131A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581284 | ||||||
chr18:49581399 | T | C | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0036g0259 | 3 | NA18975.hp1 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.794-16T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581399 | ||||||
chr18:49581736 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1036+79C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49581736 | ||||||
chr18:49581737 | A | G | 10 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(7): Show | 10 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+80A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49581737 | ||||||
chr18:49581806 | T | C | 1 | a0001c0005t0007g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1036+149T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49581806 | ||||||
chr18:49582081 | C | G | 2 | a0002c0002t0005g0340a0002c0002t0005g0367 | 2 | HG01256.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1037-281C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582081 | ||||||
chr18:49582081 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1037-281C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582081 | ||||||
chr18:49582104 | T | A | 1 | a0004c0006t0088g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1037-258T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582104 | ||||||
chr18:49582236 | G | A | 18 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(15): Show | 18 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1037-126G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582236 | ||||||
chr18:49582286 | T | G | 4 | a0001c0001t0008g0002a0001c0001t0008g0193a0001c0001t0008g0203others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-76T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582286 | ||||||
chr18:49582545 | A | G | 2 | a0001c0001t0032g0021a0001c0001t0032g0022 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1157+63A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582545 | ||||||
chr18:49582549 | C | A | 1 | a0001c0001t0001g0227 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1157+67C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582549 | ||||||
chr18:49582558 | G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0227 | 2 | HG02004.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1157+76G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582558 | ||||||
chr18:49582558 | G | T | 1 | a0001c0001t0033g0276 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1157+76G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582558 | ||||||
chr18:49582559 | T | A | 1 | a0001c0001t0033g0276 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1157+77T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582559 | ||||||
chr18:49582576 | C | T | 1 | a0002c0002t0072g0363 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1157+94C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582576 | ||||||
chr18:49582584 | A | G | 4 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157+102A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582584 | ||||||
chr18:49582648 | A | G | 16 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0039g0178others(13): Show | 16 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1157+166A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582648 | ||||||
chr18:49582710 | C | T | 2 | a0001c0001t0027g0240a0002c0002t0067g0327 | 2 | NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1157+228C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582710 | ||||||
chr18:49582750 | T | G | 3 | a0002c0002t0005g0341a0002c0002t0028g0354a0002c0002t0051g0342 | 3 | HG00642.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1157+268T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582750 | ||||||
chr18:49582773 | T | C | 5 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+291T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582773 | ||||||
chr18:49582819 | C | T | 1 | a0001c0001t0020g0375 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1157+337C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582819 | ||||||
chr18:49582835 | C | T | 12 | a0001c0001t0039g0178a0001c0001t0039g0189a0001c0001t0041g0160others(9): Show | 12 | HG02258.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1157+353C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582835 | ||||||
chr18:49582875 | GTA | G | 5 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0094g0030others(2): Show | 5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+397_1157+398d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 49582875 | |||||
chr18:49582983 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1157+501C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582983 | ||||||
chr18:49583005 | G | A | 2 | a0001c0001t0032g0021a0001c0001t0032g0022 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1157+523G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583005 | ||||||
chr18:49583007 | A | G | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1157+525A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583007 | ||||||
chr18:49583009 | G | A | 12 | a0001c0001t0039g0178a0001c0001t0039g0189a0001c0001t0041g0160others(9): Show | 12 | HG02258.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1157+527G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583009 | ||||||
chr18:49583072 | G | A | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1158-484G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583072 | ||||||
chr18:49583132 | G | C | 5 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0097g0267others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158-424G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583132 | ||||||
chr18:49583281 | C | T | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1158-275C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583281 | ||||||
chr18:49583282 | A | C | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1158-274A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583282 | ||||||
chr18:49583283 | G | A | 1 | a0001c0001t0012g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1158-273G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583283 | ||||||
chr18:49583323 | G | A | 159 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1158-233G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583323 | ||||||
chr18:49583397 | G | C | 4 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274others(1): Show | 4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-159G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583397 | ||||||
chr18:49583410 | G | A | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-146G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583410 | ||||||
chr18:49583444 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1158-112C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583444 | ||||||
chr18:49583454 | C | T | 6 | a0003c0004t0016g0145a0003c0004t0016g0146a0003c0004t0016g0148others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-102C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583454 | ||||||
chr18:49583455 | T | C | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1158-101T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583455 | ||||||
chr18:49583514 | C | T | 1 | a0002c0002t0023g0313 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1158-42C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583514 | ||||||
chr18:49583552 | G | C | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.1158-4G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583552 | ||||||
chr18:49583894 | A | T | 14 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1376+120A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49583894 | ||||||
chr18:49584057 | A | T | 1 | a0001c0001t0033g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1376+283A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584057 | ||||||
chr18:49584090 | G | A | 1 | a0002c0002t0005g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1376+316G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584090 | ||||||
chr18:49584171 | A | G | 1 | a0001c0001t0012g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1376+397A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584171 | ||||||
chr18:49584195 | T | A | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1376+421T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584195 | ||||||
chr18:49584264 | C | T | 2 | a0001c0001t0003g0056a0001c0001t0040g0053 | 2 | HG02040.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1376+490C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584264 | ||||||
chr18:49584302 | A | G | 3 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0049g0292 | 3 | HG01891.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1376+528A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584302 | ||||||
chr18:49584412 | G | A | 1 | a0001c0001t0126g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1376+638G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584412 | ||||||
chr18:49584549 | G | A | 6 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+775G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584549 | ||||||
chr18:49584596 | A | C | 12 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1376+822A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584596 | ||||||
chr18:49584890 | T | C | 66 | a0001c0001t0001g0052a0001c0001t0001g0092a0001c0001t0001g0175others(63): Show | 67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1376+1116T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584890 | ||||||
chr18:49585012 | A | G | 1 | a0001c0001t0114g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1376+1238A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585012 | ||||||
chr18:49585018 | A | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1376+1244A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585018 | ||||||
chr18:49585121 | G | A | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1376+1347G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585121 | ||||||
chr18:49585147 | C | T | 1 | a0002c0002t0066g0303 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1376+1373C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585147 | ||||||
chr18:49585192 | A | G | 286 | a0001c0001t0001g0052a0001c0001t0001g0092a0001c0001t0001g0175others(283): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1376+1418A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585192 | ||||||
chr18:49585259 | C | T | 4 | a0001c0001t0026g0270a0001c0001t0048g0271a0001c0001t0081g0269others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1376+1485C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585259 | ||||||
chr18:49585357 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-1389C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585357 | ||||||
chr18:49585362 | C | T | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1377-1384C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585362 | ||||||
chr18:49585667 | C | A | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-1079C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585667 | ||||||
chr18:49585870 | C | A | 1 | a0002c0002t0130g0171 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1377-876C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585870 | ||||||
chr18:49585939 | T | C | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-807T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585939 | ||||||
chr18:49585941 | G | C | 7 | a0001c0001t0039g0178a0001c0001t0039g0189a0001c0001t0041g0160others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377-805G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585941 | ||||||
chr18:49585942 | G | T | 7 | a0001c0001t0039g0178a0001c0001t0039g0189a0001c0001t0041g0160others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377-804G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585942 | ||||||
chr18:49585973 | G | C | 2 | a0001c0001t0084g0258a0001c0001t0085g0263 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1377-773G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585973 | ||||||
chr18:49586082 | C | T | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1377-664C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586082 | ||||||
chr18:49586199 | T | A | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-547T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586199 | ||||||
chr18:49586233 | G | T | 6 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274others(3): Show | 6 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377-513G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586233 | ||||||
chr18:49586250 | C | T | 2 | a0001c0001t0102g0143a0001c0001t0106g0144 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1377-496C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586250 | ||||||
chr18:49586251 | G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0284 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1377-495G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586251 | ||||||
chr18:49586311 | T | C | 286 | a0001c0001t0001g0052a0001c0001t0001g0092a0001c0001t0001g0175others(283): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1377-435T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586311 | ||||||
chr18:49586361 | CACTAACA others(6): Show |
C | 1 | a0001c0001t0137g0100 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1377-383_1377-371d others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | 49586361 | |||||
chr18:49586367 | C | G | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1377-379C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586367 | ||||||
chr18:49586407 | T | A | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1377-339T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586407 | ||||||
chr18:49586481 | G | GCCAT | 130 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1377-265_1377-264i others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586481 | ||||||
chr18:49586501 | T | C | 40 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(37): Show | 40 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.1377-245T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586501 | ||||||
chr18:49586574 | G | T | 26 | a0001c0001t0002g0054a0001c0001t0002g0073a0001c0001t0002g0074others(23): Show | 26 | HG00544.hp1 HG02056.hp1 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1377-172G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586574 | ||||||
chr18:49586626 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1377-120G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586626 | ||||||
chr18:49586638 | C | T | 130 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1377-108C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586638 | ||||||
chr18:49586642 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1377-104A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586642 | ||||||
chr18:49586942 | A | G | 7 | a0001c0001t0039g0178a0001c0001t0039g0189a0001c0001t0041g0160others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1481+92A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49586942 | ||||||
chr18:49586994 | C | T | 1 | a0001c0001t0018g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1481+144C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49586994 | ||||||
chr18:49587001 | G | C | 2 | a0001c0001t0038g0025a0001c0001t0038g0172 | 2 | HG02071.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1481+151G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587001 | ||||||
chr18:49587106 | T | TA | 26 | a0001c0001t0002g0261a0001c0001t0017g0285a0001c0001t0017g0287others(23): Show | 26 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1481+273dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587106 | |||||
chr18:49587106 | TA | T | 151 | a0001c0001t0001g0224a0001c0001t0003g0009a0001c0001t0003g0010others(148): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1481+273delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587106 | |||||
chr18:49587274 | CAAAA | C | 6 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0105others(3): Show | 6 | HG00738.hp2 HG01099.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1481+426_1481+429d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587274 | |||||
chr18:49587285 | A | G | 1 | a0001c0001t0098g0268 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1481+435A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587285 | ||||||
chr18:49587356 | G | C | 53 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(50): Show | 53 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.1481+506G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587356 | ||||||
chr18:49587437 | C | T | 4 | a0001c0001t0015g0001a0001c0001t0015g0027a0001c0001t0015g0028others(1): Show | 5 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+587C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587437 | ||||||
chr18:49587508 | G | A | 3 | a0001c0001t0048g0271a0001c0001t0081g0269a0001c0001t0082g0272 | 3 | HG01243.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1481+658G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587508 | ||||||
chr18:49587510 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1481+660A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587510 | ||||||
chr18:49587527 | C | T | 12 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0033g0275others(9): Show | 12 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1481+677C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587527 | ||||||
chr18:49587563 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1481+713C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587563 | ||||||
chr18:49587568 | C | CA | 139 | a0001c0001t0001g0092a0001c0001t0001g0208a0001c0001t0001g0209others(136): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1481+744dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | C | CAA | 37 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0019others(34): Show | 37 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1481+743_1481+744d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | C | CAAA | 9 | a0001c0001t0032g0021a0001c0001t0098g0268a0001c0001t0141g0250others(6): Show | 9 | HG01167.hp1 HG01346.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1481+742_1481+744d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0024g0046a0001c0001t0024g0048 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1481+735_1481+744d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0024g0047a0001c0001t0076g0049 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1481+734_1481+744d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0082g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1481+730_1481+744d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0048g0271a0001c0001t0081g0269 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1481+729_1481+744d others(18): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | CA | C | 6 | a0001c0001t0002g0073a0001c0001t0040g0112a0001c0001t0041g0160others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1481+744delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587568 | CAAAAAAA | C | 7 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0039g0178others(4): Show | 7 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1481+738_1481+744d others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | |||||
chr18:49587684 | C | T | 3 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274 | 3 | HG00738.hp1 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1481+834C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587684 | ||||||
chr18:49587789 | C | CT | 136 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1481+950dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587789 | |||||
chr18:49587841 | G | A | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+991G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587841 | ||||||
chr18:49588113 | TCTC | T | 5 | a0001c0001t0041g0160a0001c0001t0104g0163a0001c0001t0105g0162others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+1264_1481+126 others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588113 | ||||||
chr18:49588140 | C | G | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1290C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588140 | ||||||
chr18:49588199 | G | A | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1349G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588199 | ||||||
chr18:49588256 | A | G | 29 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(26): Show | 29 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1481+1406A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588256 | ||||||
chr18:49588265 | C | T | 5 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0094g0030others(2): Show | 5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+1415C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588265 | ||||||
chr18:49588282 | C | CT | 107 | a0001c0001t0001g0052a0001c0001t0001g0278a0001c0001t0001g0280others(104): Show | 107 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1481+1450dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588282 | |||||
chr18:49588282 | C | CTT | 13 | a0001c0001t0002g0117a0001c0001t0002g0135a0001c0001t0041g0160others(10): Show | 13 | HG01243.hp2 HG02015.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1481+1449_1481+145 others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588282 | |||||
chr18:49588282 | CTT | C | 15 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1481+1449_1481+145 others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588282 | |||||
chr18:49588310 | T | C | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1460T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588310 | ||||||
chr18:49588313 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1481+1463C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588313 | ||||||
chr18:49588314 | A | G | 82 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(79): Show | 82 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(79): Show |
intron_variant | MODIFIER | c.1481+1464A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588314 | ||||||
chr18:49588322 | G | A | 3 | a0001c0001t0008g0184a0001c0001t0008g0192a0001c0001t0008g0197 | 3 | HG01928.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1481+1472G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588322 | ||||||
chr18:49588329 | C | T | 2 | a0004c0006t0087g0170a0004c0006t0088g0169 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1481+1479C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588329 | ||||||
chr18:49588375 | C | T | 200 | a0001c0001t0001g0052a0001c0001t0001g0092a0001c0001t0001g0175others(197): Show | 201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1481+1525C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588375 | ||||||
chr18:49588400 | A | G | 40 | a0001c0001t0018g0071a0001c0001t0018g0130a0001c0001t0018g0141others(37): Show | 40 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.1481+1550A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588400 | ||||||
chr18:49588401 | A | C | 1 | a0001c0001t0003g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1551A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588401 | ||||||
chr18:49588402 | C | CTCCTCCA others(12): Show |
1 | a0001c0001t0003g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1552_1481+155 others(23): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588402 | ||||||
chr18:49588404 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1554T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588404 | ||||||
chr18:49588405 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1555T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588405 | ||||||
chr18:49588437 | C | T | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1587C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588437 | ||||||
chr18:49588439 | C | T | 4 | a0001c0001t0006g0079a0001c0001t0006g0122a0001c0001t0084g0258others(1): Show | 4 | HG02040.hp2 HG02080.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481+1589C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588439 | ||||||
chr18:49588480 | GCCATGTT others(10): Show |
G | 2 | a0001c0001t0039g0178a0001c0001t0039g0189 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1481+1647_1481+166 others(21): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588480 | |||||
chr18:49588582 | G | C | 21 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1481+1732G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588582 | ||||||
chr18:49588588 | C | T | 13 | a0001c0001t0055g0326a0001c0001t0107g0190a0001c0003t0007g0187others(10): Show | 13 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1481+1738C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588588 | ||||||
chr18:49588589 | G | A | 1 | a0001c0001t0142g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1481+1739G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588589 | ||||||
chr18:49588603 | A | G | 1 | a0001c0001t0141g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1481+1753A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588603 | ||||||
chr18:49588635 | A | T | 13 | a0001c0001t0024g0046a0001c0001t0024g0047a0001c0001t0024g0048others(10): Show | 13 | HG01243.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1481+1785A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588635 | ||||||
chr18:49588684 | C | T | 8 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0039g0178others(5): Show | 8 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1482-1817C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588684 | ||||||
chr18:49588705 | G | A | 2 | a0001c0001t0037g0136a0002c0002t0005g0366 | 2 | HG01099.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1482-1796G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588705 | ||||||
chr18:49588775 | C | T | 1 | a0001c0001t0096g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1482-1726C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588775 | ||||||
chr18:49588800 | A | G | 31 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(28): Show | 31 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1482-1701A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588800 | ||||||
chr18:49588833 | C | G | 2 | a0001c0001t0039g0178a0001c0001t0039g0189 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1482-1668C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588833 | ||||||
chr18:49588856 | A | C | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-1645A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588856 | ||||||
chr18:49588869 | A | G | 12 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482-1632A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588869 | ||||||
chr18:49588951 | C | T | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-1550C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588951 | ||||||
chr18:49588958 | G | A | 6 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274others(3): Show | 6 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-1543G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588958 | ||||||
chr18:49588972 | G | T | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-1529G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588972 | ||||||
chr18:49588994 | C | T | 3 | a0004c0006t0029g0265a0004c0006t0029g0266a0004c0006t0075g0264 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1482-1507C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588994 | ||||||
chr18:49589185 | A | C | 21 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482-1316A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589185 | ||||||
chr18:49589265 | C | T | 2 | a0001c0001t0032g0021a0001c0001t0032g0022 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1482-1236C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589265 | ||||||
chr18:49589303 | A | G | 21 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482-1198A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589303 | ||||||
chr18:49589369 | T | G | 6 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274others(3): Show | 6 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-1132T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589369 | ||||||
chr18:49589547 | G | T | 1 | a0001c0001t0015g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1482-954G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589547 | ||||||
chr18:49589597 | G | A | 1 | a0001c0001t0015g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1482-904G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589597 | ||||||
chr18:49589683 | A | G | 29 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(26): Show | 29 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1482-818A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589683 | ||||||
chr18:49589729 | G | A | 2 | a0001c0001t0039g0178a0001c0001t0039g0189 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1482-772G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589729 | ||||||
chr18:49589834 | T | C | 29 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(26): Show | 29 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1482-667T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589834 | ||||||
chr18:49589954 | G | C | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-547G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589954 | ||||||
chr18:49590042 | C | T | 19 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-459C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590042 | ||||||
chr18:49590060 | T | C | 21 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482-441T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590060 | ||||||
chr18:49590080 | C | A | 7 | a0001c0001t0032g0021a0001c0001t0032g0022a0001c0001t0049g0292others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482-421C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590080 | ||||||
chr18:49590169 | A | G | 2 | a0001c0001t0097g0267a0001c0001t0098g0268 | 2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1482-332A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590169 | ||||||
chr18:49590173 | T | TTG | 44 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(41): Show | 45 | HG00423.hp1 HG00544.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1482-294_1482-293d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | T | TTGTG | 73 | a0001c0001t0001g0092a0001c0001t0001g0209a0001c0001t0002g0054others(70): Show | 73 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1482-296_1482-293d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | T | TTGTGTG | 54 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0206others(51): Show | 55 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1482-298_1482-293d others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0226a0001c0001t0001g0229a0001c0001t0001g0232others(6): Show | 9 | HG01106.hp1 HG01496.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1482-300_1482-293d others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | TTG | T | 32 | a0001c0001t0006g0079a0001c0001t0011g0005a0001c0001t0011g0006others(29): Show | 32 | HG00609.hp2 HG00741.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1482-294_1482-293d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | TTGTG | T | 22 | a0001c0001t0010g0150a0001c0001t0024g0046a0001c0001t0024g0047others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.1482-296_1482-293d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | TTGTGTG | T | 17 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(14): Show | 17 | HG00735.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1482-298_1482-293d others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | TTGTGTGT others(1): Show |
T | 15 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0094g0030others(12): Show | 15 | HG02055.hp2 HG02071.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1482-300_1482-293d others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0039g0178a0001c0001t0039g0189a0001c0001t0042g0156others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1482-302_1482-293d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590173 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0010g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1482-304_1482-293d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | |||||
chr18:49590220 | G | A | 1 | a0002c0002t0021g0376 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1482-281G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590220 | ||||||
chr18:49590231 | A | C | 4 | a0001c0001t0033g0275a0001c0001t0033g0276a0001c0001t0083g0274others(1): Show | 4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482-270A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590231 | ||||||
chr18:49590305 | A | G | 71 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(68): Show | 71 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(68): Show |
intron_variant | MODIFIER | c.1482-196A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590305 | ||||||
chr18:49590340 | G | A | 3 | a0002c0002t0022g0305a0002c0002t0022g0317a0002c0002t0066g0303 | 3 | HG02155.hp2 NA18964.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1482-161G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590340 | ||||||
chr18:49590388 | T | C | 2 | a0001c0001t0039g0178a0001c0001t0039g0189 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1482-113T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590388 | ||||||
chr18:49590388 | TA | T | 6 | a0001c0001t0038g0025a0001c0001t0038g0172a0001c0001t0094g0030others(3): Show | 6 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-112delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590388 | ||||||
chr18:49590450 | G | A | 12 | a0001c0001t0017g0285a0001c0001t0017g0287a0001c0001t0017g0288others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482-51G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590450 |