geneid | 10960 |
---|---|
ensemblid | ENSG00000169223.16 |
hgncid | 16986 |
symbol | LMAN2 |
name | lectin, mannose binding 2 |
refseq_nuc | NM_006816.3 |
refseq_prot | NP_006807.1 |
ensembl_nuc | ENST00000303127.12 |
ensembl_prot | ENSP00000303366.7 |
mane_status | MANE Select |
chr | chr5 |
start | 177331567 |
end | 177351668 |
strand | - |
ver | v1.2 |
region | chr5:177331567-177351668 |
region5000 | chr5:177326567-177356668 |
regionname0 | LMAN2_chr5_177331567_177351668 |
regionname5000 | LMAN2_chr5_177326567_177356668 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 356 | 368 | 98 | 70 | 143 | 15 | 40 | 107 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0002 | 0/0 | 356 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0003 | 0/0 | 356 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0004 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0005 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1071 | 363 | 94 | 69 | 143 | 15 | 40 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0002 | 0/0 | 1071 | 5 | 0 | 0 | 5 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0003 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0004 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0005 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0006 | 0/0 | 1071 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0007 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0008 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0009 | 0/0 | 1071 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
c0010 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 541 | 312 | 49 | 63 | 144 | 14 | 40 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0002 | 0/0 | 541 | 32 | 28 | 2 | 0 | 2 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0003 | 0/0 | 541 | 23 | 23 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0004 | 0/0 | 541 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0005 | 0/0 | 541 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0006 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0007 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0008 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0009 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
t0010 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 0 | 2 | 15 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0002 | 1/0 | 14 | 0 | 0 | 10 | 1 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0003 | 0/0 | 10 | 0 | 6 | 3 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0007 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0008 | 0/0 | 6 | 1 | 2 | 0 | 1 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0012 | 0/1 | 3 | 1 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1071 | 363 | 94 | 69 | 143 | 15 | 40 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0005 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0007 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0008 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0009 | 0/0 | 1071 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0010 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0002c0002 | 0/0 | 1071 | 5 | 0 | 0 | 5 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0003c0006 | 0/0 | 1071 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0004c0004 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0005c0003 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1611 | 302 | 45 | 63 | 139 | 13 | 40 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0002 | 0/0 | 1611 | 32 | 28 | 2 | 0 | 2 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0003 | 0/0 | 1611 | 21 | 21 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0004 | 0/0 | 1611 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0005 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0007 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0008 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0009 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0001t0010 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0005t0003 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0007t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0008t0003 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0009t0006 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0001c0010t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0002c0002t0001 | 0/0 | 1611 | 5 | 0 | 0 | 5 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0003c0006t0001 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0004c0004t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
a0005c0003t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | copy fasta | chr5 | 177326567 | 177356668 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 2 | 15 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0002 | 1/0 | 14 | 0 | 0 | 10 | 1 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0003 | 0/0 | 10 | 0 | 6 | 3 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0008 | 0/0 | 6 | 1 | 2 | 0 | 1 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0012 | 0/1 | 3 | 1 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0009g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0005t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0007t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0008t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0009t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0001c0010t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0003c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
a0005c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00733 | hp2 | a0001 | c0009 | t0006 | g0107 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0080 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01255 | hp1 | a0001 | c0001 | t0010 | g0101 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0252 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02970 | hp1 | a0001 | c0010 | t0001 | g0126 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03130 | hp1 | a0001 | c0005 | t0003 | g0043 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03225 | hp1 | a0001 | c0007 | t0001 | g0247 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03453 | hp1 | a0004 | c0004 | t0001 | g0042 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18522 | hp2 | a0005 | c0003 | t0001 | g0041 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19090 | hp1 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ASW | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20752 | hp1 | a0003 | c0006 | t0001 | g0160 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | GIH | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
NA21309 | hp2 | a0001 | c0008 | t0003 | g0244 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:177332169
|
C | T | 1 | a0003 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.988G>A | p.Ala330Thr | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 1009/1611 | 988/1071 | 330/356 | chr5 | 177332169 | ||
chr5:177334335
|
T | C | 1 | a0002 | 5 | NA18945.hp1 NA18947.hp2 NA18977.hp1 others(2): Show |
missense_variant | MODERATE | c.859A>G | p.Ile287Val | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/8 | 880/1611 | 859/1071 | 287/356 | chr5 | 177334335 | ||
chr5:177351454
|
T | C | 1 | a0005 | 1 | NA18522.hp2 | missense_variant&splice_region_variant | MODERATE | c.194A>G | p.Gln65Arg | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 215/1611 | 194/1071 | 65/356 | chr5 | 177351454 | ||
chr5:177351532
|
A | G | 1 | a0004 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.116T>C | p.Leu39Ser | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 137/1611 | 116/1071 | 39/356 | chr5 | 177351532 | ||
chr5:177351599
|
G | T | 1 | a0005 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.49C>A | p.Leu17Met | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 70/1611 | 49/1071 | 17/356 | chr5 | 177351599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:177332212
|
G | A | 1 | a0001c0007 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.945C>T | p.Ser315Ser | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 966/1611 | 945/1071 | 315/356 | chr5 | 177332212 | ||
chr5:177337146
|
G | A | 1 | a0001c0008 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.780C>T | p.Gly260Gly | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/8 | 801/1611 | 780/1071 | 260/356 | chr5 | 177337146 | ||
chr5:177337179
|
G | A | 1 | a0001c0009 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.747C>T | p.Thr249Thr | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/8 | 768/1611 | 747/1071 | 249/356 | chr5 | 177337179 | ||
chr5:177337435
|
G | A | 1 | a0001c0009 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.603C>T | p.Gly201Gly | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 5/8 | 624/1611 | 603/1071 | 201/356 | chr5 | 177337435 | ||
chr5:177337738
|
G | A | 1 | a0001c0010 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.481C>T | p.Leu161Leu | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/8 | 502/1611 | 481/1071 | 161/356 | chr5 | 177337738 | ||
chr5:177351215
|
G | T | 1 | a0005c0003 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.273C>A | p.Thr91Thr | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/8 | 294/1611 | 273/1071 | 91/356 | chr5 | 177351215 | ||
chr5:177351477
|
C | T | 1 | a0001c0005 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.171G>A | p.Glu57Glu | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 192/1611 | 171/1071 | 57/356 | chr5 | 177351477 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:177331617
|
C | T | 1 | a0001c0001t0004 | 2 | HG01496.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*469G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 469 | chr5 | 177331617 | |||||
chr5:177331640
|
A | C | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 446 | chr5 | 177331640 | |||||
chr5:177331695
|
G | A | 1 | a0001c0001t0005 | 2 | NA18943.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*391C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 391 | chr5 | 177331695 | |||||
chr5:177331708
|
G | A | 1 | a0001c0001t0009 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 378 | chr5 | 177331708 | |||||
chr5:177331734
|
A | C | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 352 | chr5 | 177331734 | |||||
chr5:177331778
|
C | T | 3 | a0001c0001t0003a0001c0005t0003a0001c0008t0003 | 23 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*308G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 308 | chr5 | 177331778 | |||||
chr5:177331785
|
C | T | 1 | a0001c0001t0002 | 32 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*301G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 301 | chr5 | 177331785 | |||||
chr5:177331800
|
C | T | 1 | a0001c0001t0008 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 286 | chr5 | 177331800 | |||||
chr5:177331970
|
A | C | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 116 | chr5 | 177331970 | |||||
chr5:177332071
|
C | T | 1 | a0001c0009t0006 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 15 | chr5 | 177332071 | |||||
chr5:177332075
|
G | A | 1 | a0001c0001t0010 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 11 | chr5 | 177332075 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:177332303
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.911-57G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332303 | ||||||
chr5:177332343
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0002g0219a0001c0001t0002g0222others(5): Show | 9 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.911-97G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332343 | ||||||
chr5:177332422
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.911-176G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332422 | ||||||
chr5:177332532
|
T | G | 4 | a0001c0001t0003g0044a0001c0001t0003g0215a0001c0001t0003g0226others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-286A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332532 | ||||||
chr5:177332552
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.911-306T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332552 | ||||||
chr5:177332655
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0254a0001c0001t0002g0255 | 4 | HG02055.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-409G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332655 | ||||||
chr5:177332690
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.911-444G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332690 | ||||||
chr5:177332777
|
C | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(39): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.911-531G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332777 | ||||||
chr5:177333068
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0149 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-822G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333068 | ||||||
chr5:177333114
|
C | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0149 | 3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-868G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333114 | ||||||
chr5:177333123
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0149 | 3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-877G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333123 | ||||||
chr5:177333130
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.911-884A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333130 | ||||||
chr5:177333221
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0125 | 2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.911-975G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333221 | ||||||
chr5:177333226
|
A | C | 108 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(105): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.911-980T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333226 | ||||||
chr5:177333266
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0069others(2): Show | 11 | HG01255.hp1 HG01258.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.910+1018C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333266 | ||||||
chr5:177333271
|
T | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+1013A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333271 | ||||||
chr5:177333436
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.910+848A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333436 | ||||||
chr5:177333570
|
T | C | 1 | a0001c0008t0003g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910+714A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333570 | ||||||
chr5:177333615
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.910+669G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333615 | ||||||
chr5:177333650
|
G | T | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.910+634C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333650 | ||||||
chr5:177333851
|
CACG | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(84): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.910+430_910+432del others(3): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333851 | ||||||
chr5:177333904
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0120 | 2 | HG00558.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.910+380G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333904 | ||||||
chr5:177334042
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.910+242G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177334042 | ||||||
chr5:177334094
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.910+190G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177334094 | ||||||
chr5:177334231
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.910+53G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177334231 | ||||||
chr5:177334455
|
C | T | 3 | a0001c0001t0003g0240a0001c0001t0003g0245a0001c0001t0003g0248 | 3 | HG02572.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.791-52G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334455 | ||||||
chr5:177334534
|
A | G | 114 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(111): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.791-131T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334534 | ||||||
chr5:177334535
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-132C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334535 | ||||||
chr5:177334538
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.791-135C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334538 | ||||||
chr5:177334620
|
G | C | 2 | a0001c0001t0003g0004a0001c0001t0003g0214 | 10 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.791-217C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334620 | ||||||
chr5:177334621
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.791-218C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334621 | ||||||
chr5:177334924
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.791-521T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334924 | ||||||
chr5:177335044
|
T | A | 1 | a0001c0005t0003g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.791-641A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335044 | ||||||
chr5:177335051
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.791-648C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335051 | ||||||
chr5:177335232
|
G | A | 14 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229others(11): Show | 22 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.791-829C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335232 | ||||||
chr5:177335258
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.791-855G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335258 | ||||||
chr5:177335326
|
C | T | 2 | a0001c0001t0003g0004a0001c0001t0003g0214 | 10 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.791-923G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335326 | ||||||
chr5:177335449
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.791-1046G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335449 | ||||||
chr5:177336265
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01109.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.790+871C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336265 | ||||||
chr5:177336432
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.790+704A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336432 | ||||||
chr5:177336444
|
G | A | 6 | a0001c0001t0003g0004a0001c0001t0003g0214a0001c0001t0003g0236others(3): Show | 14 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.790+692C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336444 | ||||||
chr5:177336487
|
A | C | 21 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229others(18): Show | 29 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.790+649T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336487 | ||||||
chr5:177336642
|
T | C | 2 | a0001c0001t0003g0004a0001c0001t0003g0214 | 10 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.790+494A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336642 | ||||||
chr5:177336655
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.790+481C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336655 | ||||||
chr5:177336662
|
T | C | 16 | a0001c0001t0001g0246a0001c0001t0003g0004a0001c0001t0003g0044others(13): Show | 24 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.790+474A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336662 | ||||||
chr5:177336794
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.790+342A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336794 | ||||||
chr5:177336834
|
G | C | 5 | a0001c0001t0001g0061a0001c0001t0001g0082a0001c0001t0001g0102others(2): Show | 5 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+302C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336834 | ||||||
chr5:177336855
|
AAGG | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(84): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.790+278_790+280del others(3): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336855 | ||||||
chr5:177336951
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.790+185G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336951 | ||||||
chr5:177336986
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.790+150C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336986 | ||||||
chr5:177337107
|
G | A | 14 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0068others(11): Show | 16 | HG00408.hp1 HG01099.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.790+29C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177337107 | ||||||
chr5:177337339
|
A | AC | 8 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0090others(5): Show | 8 | HG00597.hp2 HG01517.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+23dupG | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 5/7 | chr5 | 177337339 | ||||||
chr5:177337584
|
C | A | 1 | a0001c0001t0001g0087 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.514-60G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/7 | chr5 | 177337584 | ||||||
chr5:177337655
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.513+51G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/7 | chr5 | 177337655 | ||||||
chr5:177337684
|
G | A | 1 | a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.513+22C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/7 | chr5 | 177337684 | ||||||
chr5:177338043
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.434-258C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338043 | ||||||
chr5:177338332
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.433+156G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338332 | ||||||
chr5:177338366
|
T | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.433+122A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338366 | ||||||
chr5:177338394
|
G | A | 108 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(105): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.433+94C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338394 | ||||||
chr5:177338863
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.316-258C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177338863 | ||||||
chr5:177338904
|
A | C | 1 | a0001c0001t0002g0021 | 3 | HG02451.hp2 HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.316-299T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177338904 | ||||||
chr5:177338988
|
T | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(102): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.316-383A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177338988 | ||||||
chr5:177339103
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0149 | 3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316-498C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339103 | ||||||
chr5:177339176
|
A | G | 132 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(129): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.316-571T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339176 | ||||||
chr5:177339186
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0046others(7): Show | 18 | HG02040.hp2 HG02071.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-581C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339186 | ||||||
chr5:177339195
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-590T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339195 | ||||||
chr5:177339456
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-851C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339456 | ||||||
chr5:177339542
|
A | T | 23 | a0001c0001t0001g0220a0001c0001t0002g0006a0001c0001t0002g0021others(20): Show | 34 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.316-937T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339542 | ||||||
chr5:177339545
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0214a0001c0001t0003g0236others(3): Show | 14 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-940G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339545 | ||||||
chr5:177339546
|
G | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(84): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-941C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339546 | ||||||
chr5:177339586
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.316-981A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339586 | ||||||
chr5:177339865
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-1260A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339865 | ||||||
chr5:177339868
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0117a0001c0001t0001g0127 | 3 | HG01099.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.316-1263C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339868 | ||||||
chr5:177340101
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.316-1496T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340101 | ||||||
chr5:177340291
|
A | C | 4 | a0001c0001t0003g0044a0001c0001t0003g0215a0001c0001t0003g0226others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-1686T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340291 | ||||||
chr5:177340419
|
A | G | 23 | a0001c0001t0001g0220a0001c0001t0002g0006a0001c0001t0002g0021others(20): Show | 34 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.316-1814T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340419 | ||||||
chr5:177340520
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.316-1915C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340520 | ||||||
chr5:177340672
|
A | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0204 | 2 | HG02109.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.316-2067T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340672 | ||||||
chr5:177340676
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.316-2071C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340676 | ||||||
chr5:177340766
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-2161A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340766 | ||||||
chr5:177340786
|
A | G | 1 | a0001c0001t0002g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.316-2181T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340786 | ||||||
chr5:177340789
|
C | CT | 2 | a0001c0001t0001g0020a0001c0001t0001g0207 | 4 | HG00639.hp1 HG03654.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-2185dupA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340789 | ||||||
chr5:177340816
|
A | G | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(84): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-2211T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340816 | ||||||
chr5:177340881
|
A | T | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-2276T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340881 | ||||||
chr5:177340916
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.316-2311C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340916 | ||||||
chr5:177340975
|
A | T | 1 | a0001c0001t0001g0015 | 3 | NA18948.hp2 NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.316-2370T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340975 | ||||||
chr5:177340976
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-2371G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340976 | ||||||
chr5:177340977
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.316-2372C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340977 | ||||||
chr5:177341002
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0070others(6): Show | 14 | HG01256.hp1 HG01981.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-2397T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341002 | ||||||
chr5:177341064
|
C | CT | 13 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0067others(10): Show | 15 | HG01109.hp1 HG01981.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.316-2460dupA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341064 | ||||||
chr5:177341064
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.316-2459G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341064 | ||||||
chr5:177341064
|
CT | C | 101 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(98): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.316-2460delA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341064 | ||||||
chr5:177341065
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.316-2460A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341065 | ||||||
chr5:177341070
|
T | C | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.316-2465A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341070 | ||||||
chr5:177341089
|
A | G | 108 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(105): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.316-2484T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341089 | ||||||
chr5:177341109
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(84): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-2504G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341109 | ||||||
chr5:177341184
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-2579T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341184 | ||||||
chr5:177341223
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0175 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.316-2618G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341223 | ||||||
chr5:177341255
|
G | A | 1 | a0001c0009t0006g0107 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.316-2650C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341255 | ||||||
chr5:177341346
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0105 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.316-2741C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341346 | ||||||
chr5:177341361
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.316-2756G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341361 | ||||||
chr5:177341404
|
G | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG02145.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.316-2799C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341404 | ||||||
chr5:177341565
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.316-2960T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341565 | ||||||
chr5:177341590
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.316-2985C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341590 | ||||||
chr5:177341894
|
T | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0046others(8): Show | 19 | HG02040.hp2 HG02071.hp2 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.316-3289A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341894 | ||||||
chr5:177341997
|
TA | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0074a0001c0001t0001g0090 | 4 | HG03704.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-3393delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341997 | ||||||
chr5:177342168
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.316-3563G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342168 | ||||||
chr5:177342230
|
G | A | 5 | a0001c0001t0003g0239a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 5 | HG02572.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-3625C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342230 | ||||||
chr5:177342352
|
T | A | 1 | a0001c0001t0001g0025 | 2 | NA18968.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.316-3747A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342352 | ||||||
chr5:177342423
|
C | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0211others(1): Show | 4 | HG00423.hp2 NA18949.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-3818G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342423 | ||||||
chr5:177342505
|
T | C | 1 | a0001c0001t0002g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.316-3900A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342505 | ||||||
chr5:177342898
|
C | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0136others(2): Show | 6 | HG00597.hp1 HG02132.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-4293G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342898 | ||||||
chr5:177343099
|
A | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02572.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-4494T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343099 | ||||||
chr5:177343241
|
G | C | 1 | a0001c0001t0001g0037 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.316-4636C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343241 | ||||||
chr5:177343280
|
T | C | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.316-4675A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343280 | ||||||
chr5:177343323
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0229 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.316-4718A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343323 | ||||||
chr5:177343406
|
G | C | 1 | a0001c0001t0003g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-4801C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343406 | ||||||
chr5:177343564
|
G | GAC | 7 | a0001c0001t0001g0063a0001c0001t0001g0084a0001c0001t0001g0085others(4): Show | 7 | HG00733.hp2 HG02083.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.316-4961_316-4960d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343564 | ||||||
chr5:177343564
|
GAC | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0019others(29): Show | 43 | HG00642.hp1 HG01123.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.316-4961_316-4960d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343564 | ||||||
chr5:177343584
|
C | CACACACA others(41): Show |
9 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0234others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(50): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACACA others(39): Show |
1 | a0001c0001t0001g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.316-4980_316-4979i others(48): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACACA others(37): Show |
54 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(51): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(46): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACACA others(39): Show |
1 | a0001c0001t0001g0037 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(48): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACACA others(35): Show |
9 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0002g0038others(6): Show | 11 | HG01167.hp2 HG02647.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(44): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACACA others(33): Show |
15 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0040others(12): Show | 24 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(42): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACACG others(31): Show |
3 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(40): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACACGGA others(29): Show |
3 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0149 | 3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(38): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACATGGA others(29): Show |
3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(38): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343584
|
C | CACGGAAT others(27): Show |
16 | a0001c0001t0001g0246a0001c0001t0003g0004a0001c0001t0003g0044others(13): Show | 24 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(36): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | ||||||
chr5:177343686
|
G | A | 10 | a0001c0001t0001g0246a0001c0001t0003g0044a0001c0001t0003g0215others(7): Show | 10 | HG02258.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-5081C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343686 | ||||||
chr5:177343695
|
T | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-5090A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343695 | ||||||
chr5:177343855
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.316-5250C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343855 | ||||||
chr5:177343964
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-5359G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343964 | ||||||
chr5:177344144
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-5539C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344144 | ||||||
chr5:177344176
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.316-5571G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344176 | ||||||
chr5:177344210
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-5605G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344210 | ||||||
chr5:177344211
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-5606G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344211 | ||||||
chr5:177344222
|
TA | T | 8 | a0001c0001t0001g0047a0001c0001t0001g0189a0001c0001t0001g0208others(5): Show | 8 | HG02572.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-5618delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344222 | ||||||
chr5:177344235
|
A | T | 1 | a0001c0001t0003g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-5630T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344235 | ||||||
chr5:177344281
|
C | CT | 16 | a0001c0001t0001g0072a0001c0001t0001g0096a0001c0001t0001g0097others(13): Show | 16 | HG00597.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.316-5677dupA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344281 | ||||||
chr5:177344281
|
CT | C | 102 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0020others(99): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.316-5677delA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344281 | ||||||
chr5:177344281
|
CTT | C | 13 | a0001c0001t0001g0177a0001c0001t0001g0185a0001c0001t0001g0216others(10): Show | 21 | HG01243.hp1 HG01516.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.316-5678_316-5677d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344281 | ||||||
chr5:177344285
|
T | C | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-5680A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344285 | ||||||
chr5:177344470
|
C | T | 6 | a0001c0001t0001g0119a0001c0001t0001g0171a0001c0001t0001g0181others(3): Show | 6 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-5865G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344470 | ||||||
chr5:177344471
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.316-5866C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344471 | ||||||
chr5:177344762
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.316-6157G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344762 | ||||||
chr5:177344813
|
GGAAAATC others(34): Show |
G | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-6249_316-6209d others(43): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344813 | ||||||
chr5:177344897
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0229 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.315+6276G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344897 | ||||||
chr5:177344931
|
G | A | 7 | a0001c0001t0001g0246a0001c0001t0003g0004a0001c0001t0003g0214others(4): Show | 15 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.315+6242C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344931 | ||||||
chr5:177344935
|
A | AAGAAGAG others(3): Show |
10 | a0001c0001t0001g0246a0001c0001t0003g0044a0001c0001t0003g0215others(7): Show | 10 | HG02258.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.315+6228_315+6237d others(12): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344935 | ||||||
chr5:177344935
|
A | AGAGAAAG others(8): Show |
6 | a0001c0001t0003g0004a0001c0001t0003g0214a0001c0001t0003g0236others(3): Show | 14 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.315+6237_315+6238i others(17): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344935 | ||||||
chr5:177344958
|
GAAGA | G | 1 | a0001c0001t0001g0014 | 3 | HG01106.hp2 NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.315+6211_315+6214d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344958 | ||||||
chr5:177345026
|
C | G | 16 | a0001c0001t0001g0246a0001c0001t0003g0004a0001c0001t0003g0044others(13): Show | 24 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.315+6147G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345026 | ||||||
chr5:177345177
|
C | CA | 11 | a0001c0001t0001g0020a0001c0001t0001g0064a0001c0001t0001g0090others(8): Show | 13 | HG00639.hp1 HG01192.hp2 HG03654.hp2 others(10): Show |
intron_variant | MODIFIER | c.315+5995dupT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345177 | ||||||
chr5:177345177
|
CA | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0115a0001c0001t0001g0166others(4): Show | 7 | HG01167.hp2 HG02897.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+5995delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345177 | ||||||
chr5:177345339
|
T | TA | 20 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0069others(17): Show | 21 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.315+5833dupT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | ||||||
chr5:177345339
|
T | TAA | 68 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(65): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.315+5832_315+5833d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | ||||||
chr5:177345339
|
T | TAAA | 9 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0187others(6): Show | 9 | HG01192.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.315+5831_315+5833d others(5): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | ||||||
chr5:177345339
|
TA | T | 27 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0071others(24): Show | 35 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(32): Show |
intron_variant | MODIFIER | c.315+5833delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | ||||||
chr5:177345646
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0112 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.315+5527C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345646 | ||||||
chr5:177345730
|
G | GGCAT | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0234others(1): Show | 4 | HG01891.hp1 HG02723.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+5439_315+5442d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345730 | ||||||
chr5:177345730
|
GGCAT | G | 33 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0052others(30): Show | 36 | HG00423.hp2 HG00733.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.315+5439_315+5442d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345730 | ||||||
chr5:177345732
|
C | CATTT | 11 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0030others(8): Show | 16 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.315+5440_315+5441i others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345732 | ||||||
chr5:177345735
|
G | T | 51 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0020others(48): Show | 76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.315+5438C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345735 | ||||||
chr5:177345736
|
C | CATTCATT others(1): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0025others(2): Show | 13 | HG01258.hp1 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.315+5436_315+5437i others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | ||||||
chr5:177345736
|
C | CATTT | 67 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.315+5433_315+5436d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | ||||||
chr5:177345736
|
C | CATTTATT others(1): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0060others(8): Show | 21 | HG00558.hp1 HG00597.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.315+5429_315+5436d others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | ||||||
chr5:177345736
|
C | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0020others(49): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.315+5437G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | ||||||
chr5:177345736
|
CATTT | C | 17 | a0001c0001t0001g0047a0001c0001t0001g0056a0001c0001t0001g0057others(14): Show | 25 | HG01243.hp1 HG02071.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.315+5433_315+5436d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | ||||||
chr5:177345736
|
CATTTATT others(1): Show |
C | 12 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0046others(9): Show | 20 | HG02040.hp2 HG02523.hp1 HG03098.hp1 others(17): Show |
intron_variant | MODIFIER | c.315+5429_315+5436d others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | ||||||
chr5:177345739
|
T | G | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+5434A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345739 | ||||||
chr5:177345740
|
T | C | 2 | a0001c0001t0001g0037a0005c0003t0001g0041 | 3 | HG02258.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.315+5433A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345740 | ||||||
chr5:177345785
|
T | A | 1 | a0001c0001t0001g0155 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+5388A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345785 | ||||||
chr5:177345798
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0167a0001c0001t0001g0175others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+5375G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345798 | ||||||
chr5:177345870
|
C | T | 1 | a0001c0008t0003g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.315+5303G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345870 | ||||||
chr5:177345979
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.315+5194C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345979 | ||||||
chr5:177345987
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.315+5186G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345987 | ||||||
chr5:177346090
|
T | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(106): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+5083A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346090 | ||||||
chr5:177346224
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315+4949T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346224 | ||||||
chr5:177346238
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.315+4935G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346238 | ||||||
chr5:177346412
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+4761A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346412 | ||||||
chr5:177346412
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.315+4761A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346412 | ||||||
chr5:177346635
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.315+4538C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346635 | ||||||
chr5:177346651
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.315+4522A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346651 | ||||||
chr5:177346669
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.315+4504T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346669 | ||||||
chr5:177346732
|
A | G | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.315+4441T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346732 | ||||||
chr5:177347017
|
C | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(87): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.315+4156G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347017 | ||||||
chr5:177347041
|
T | G | 5 | a0001c0001t0001g0246a0001c0001t0003g0044a0001c0001t0003g0215others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+4132A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347041 | ||||||
chr5:177347127
|
A | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.315+4046T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347127 | ||||||
chr5:177347134
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.315+4039G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347134 | ||||||
chr5:177347402
|
G | A | 90 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(87): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.315+3771C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347402 | ||||||
chr5:177347452
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315+3721A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347452 | ||||||
chr5:177347973
|
A | T | 1 | a0001c0001t0001g0023 | 2 | NA18946.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.315+3200T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347973 | ||||||
chr5:177347981
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.315+3192G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347981 | ||||||
chr5:177348232
|
A | G | 3 | a0001c0001t0003g0004a0001c0001t0003g0214a0001c0001t0003g0236 | 11 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.315+2941T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348232 | ||||||
chr5:177348292
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.315+2881G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348292 | ||||||
chr5:177348384
|
C | G | 23 | a0001c0001t0001g0220a0001c0001t0002g0006a0001c0001t0002g0021others(20): Show | 34 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.315+2789G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348384 | ||||||
chr5:177348661
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.315+2512G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348661 | ||||||
chr5:177348687
|
C | CA | 49 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.315+2485dupT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348687 | ||||||
chr5:177348687
|
CA | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(69): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.315+2485delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348687 | ||||||
chr5:177348687
|
CAA | C | 18 | a0001c0001t0001g0049a0001c0001t0001g0171a0001c0001t0001g0172others(15): Show | 26 | HG01167.hp1 HG01243.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.315+2484_315+2485d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348687 | ||||||
chr5:177348815
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.315+2358G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348815 | ||||||
chr5:177348850
|
C | T | 56 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(53): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.315+2323G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348850 | ||||||
chr5:177348878
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.315+2295G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348878 | ||||||
chr5:177348883
|
CA | C | 89 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(86): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.315+2289delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348883 | ||||||
chr5:177348883
|
CAA | C | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG01069.hp2 HG01168.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+2288_315+2289d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348883 | ||||||
chr5:177349273
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.315+1900C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349273 | ||||||
chr5:177349303
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0046others(7): Show | 18 | HG02040.hp2 HG02071.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.315+1870C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349303 | ||||||
chr5:177349363
|
T | G | 1 | a0001c0001t0001g0249 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.315+1810A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349363 | ||||||
chr5:177349533
|
GATGAAGG others(7): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.315+1626_315+1639d others(16): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349533 | ||||||
chr5:177349799
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.315+1374A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349799 | ||||||
chr5:177349848
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.315+1325C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349848 | ||||||
chr5:177349957
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.315+1216C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349957 | ||||||
chr5:177350021
|
A | C | 108 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(105): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.315+1152T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350021 | ||||||
chr5:177350234
|
A | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+939T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350234 | ||||||
chr5:177350249
|
A | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+924T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350249 | ||||||
chr5:177350250
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+923C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350250 | ||||||
chr5:177350251
|
A | G | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+922T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350251 | ||||||
chr5:177350290
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+883A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350290 | ||||||
chr5:177350292
|
A | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+881T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350292 | ||||||
chr5:177350294
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+879C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350294 | ||||||
chr5:177350304
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+869C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350304 | ||||||
chr5:177350324
|
G | A | 5 | a0001c0001t0002g0040a0001c0001t0002g0252a0001c0001t0002g0253others(2): Show | 6 | HG01515.hp2 HG01517.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+849C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350324 | ||||||
chr5:177350341
|
C | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+832G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350341 | ||||||
chr5:177350399
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.315+774T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350399 | ||||||
chr5:177350441
|
C | G | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+732G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350441 | ||||||
chr5:177350442
|
T | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+731A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350442 | ||||||
chr5:177350443
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+730C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350443 | ||||||
chr5:177350445
|
T | G | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+728A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350445 | ||||||
chr5:177350450
|
T | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+723A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350450 | ||||||
chr5:177350492
|
G | A | 107 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(104): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.315+681C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350492 | ||||||
chr5:177350497
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.315+676C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350497 | ||||||
chr5:177350559
|
G | T | 1 | a0001c0001t0004g0022 | 2 | HG01496.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.315+614C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350559 | ||||||
chr5:177350587
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+586C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350587 | ||||||
chr5:177350588
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+585C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350588 | ||||||
chr5:177350589
|
T | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+584A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350589 | ||||||
chr5:177350590
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+583C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350590 | ||||||
chr5:177350595
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+578C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350595 | ||||||
chr5:177350597
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+576C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350597 | ||||||
chr5:177350598
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+575A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350598 | ||||||
chr5:177350602
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+571C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350602 | ||||||
chr5:177350603
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+570A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350603 | ||||||
chr5:177350606
|
A | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+567T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350606 | ||||||
chr5:177350609
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+564C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350609 | ||||||
chr5:177350611
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+562C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350611 | ||||||
chr5:177350612
|
T | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+561A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350612 | ||||||
chr5:177350613
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+560C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350613 | ||||||
chr5:177350615
|
A | ACCCCCCA others(94): Show |
1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+557_315+558ins others(101): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350615 | ||||||
chr5:177350617
|
TGCTGGGC others(64): Show |
T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+485_315+555del others(71): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350617 | ||||||
chr5:177350748
|
A | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+425T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350748 | ||||||
chr5:177350749
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+424A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350749 | ||||||
chr5:177350750
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+423C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350750 | ||||||
chr5:177350822
|
A | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+351T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350822 | ||||||
chr5:177350823
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+350C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350823 | ||||||
chr5:177350826
|
GGTTCAAG others(3): Show |
G | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+337_315+346del others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350826 | ||||||
chr5:177350844
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+329A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350844 | ||||||
chr5:177350861
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+312A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350861 | ||||||
chr5:177350914
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.315+259T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350914 | ||||||
chr5:177350963
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+210C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350963 | ||||||
chr5:177350968
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+205C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350968 | ||||||
chr5:177351057
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+116C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351057 | ||||||
chr5:177351082
|
A | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+91T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351082 | ||||||
chr5:177351101
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+72C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351101 | ||||||
chr5:177351103
|
C | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+70G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351103 | ||||||
chr5:177351104
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+69A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351104 | ||||||
chr5:177351105
|
C | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+68G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351105 | ||||||
chr5:177351107
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+66C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351107 | ||||||
chr5:177351110
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+63C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351110 | ||||||
chr5:177351113
|
C | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+60G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351113 | ||||||
chr5:177351114
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+59C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351114 | ||||||
chr5:177351115
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+58C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351115 | ||||||
chr5:177351116
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+57C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351116 | ||||||
chr5:177351118
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+55C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351118 | ||||||
chr5:177351119
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+54C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351119 | ||||||
chr5:177351122
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+51C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351122 | ||||||
chr5:177351123
|
G | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+50C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351123 | ||||||
chr5:177351124
|
G | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+49C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351124 | ||||||
chr5:177351167
|
A | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.315+6T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351167 | ||||||
chr5:177351169
|
T | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.315+4A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351169 | ||||||
chr5:177351373
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196+79T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351373 | ||||||
chr5:177351414
|
C | A | 1 | a0001c0001t0001g0257 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.196+38G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351414 | ||||||
chr5:177351445
|
G | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.196+7C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351445 | ||||||
chr5:177351449
|
C | T | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.196+3G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351449 | ||||||
chr5:177351450
|
A | C | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | splice_donor_variant&intron_variant | HIGH | c.196+2T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351450 | ||||||
chr5:177351451
|
C | A | 1 | a0005c0003t0001g0041 | 1 | NA18522.hp2 | splice_donor_variant&intron_variant | HIGH | c.196+1G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351451 |