Item | Value |
---|---|
geneid | 55366 |
ensemblid | ENSG00000205213.14 |
hgncid | 13299 |
symbol | LGR4 |
name | leucine rich repeat containing G protein-coupled receptor 4 |
refseq_nuc | NM_018490.5 |
refseq_prot | NP_060960.2 |
ensembl_nuc | ENST00000379214.9 |
ensembl_prot | ENSP00000368516.4 |
mane_status | MANE Select |
chr | chr11 |
start | 27365961 |
end | 27472790 |
strand | - |
ver | v1.2 |
region | chr11:27365961-27472790 |
region5000 | chr11:27360961-27477790 |
regionname0 | LGR4_chr11_27365961_27472790 |
regionname5000 | LGR4_chr11_27360961_27477790 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 951 | 223 | 57 | 35 | 99 | 12 | 18 | 78 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0002 | 0/0 | 951 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0003 | 0/0 | 951 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0004 | 0/0 | 951 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0005 | 0/0 | 951 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0006 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0007 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2856 | 128 | 24 | 24 | 60 | 7 | 13 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0002 | 0/1 | 2856 | 82 | 23 | 11 | 38 | 4 | 5 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0003 | 0/0 | 2856 | 10 | 9 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0004 | 0/0 | 2856 | 6 | 6 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0005 | 0/0 | 2856 | 4 | 4 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0006 | 0/0 | 2856 | 3 | 2 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0007 | 0/0 | 2856 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0008 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0009 | 0/0 | 2856 | 2 | 0 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0010 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0011 | 1/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0012 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0013 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
c0014 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2395 | 31 | 9 | 8 | 9 | 2 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0002 | 0/0 | 2395 | 30 | 1 | 7 | 20 | 1 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0003 | 0/0 | 2395 | 27 | 3 | 6 | 12 | 3 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0004 | 0/1 | 2395 | 25 | 3 | 4 | 14 | 2 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0005 | 0/0 | 2395 | 22 | 8 | 5 | 3 | 3 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0006 | 1/0 | 2395 | 17 | 14 | 0 | 2 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0007 | 0/0 | 2395 | 15 | 5 | 3 | 5 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0008 | 0/0 | 2395 | 12 | 0 | 2 | 10 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0009 | 0/0 | 2395 | 9 | 6 | 0 | 3 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0010 | 0/0 | 2395 | 6 | 3 | 0 | 1 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0011 | 0/0 | 2395 | 6 | 0 | 0 | 5 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0012 | 0/0 | 2395 | 6 | 0 | 0 | 6 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0013 | 0/0 | 2395 | 5 | 5 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0014 | 0/0 | 2395 | 4 | 4 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0015 | 0/0 | 2395 | 3 | 0 | 0 | 3 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0016 | 0/0 | 2395 | 3 | 0 | 3 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0017 | 0/0 | 2395 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0018 | 0/0 | 2395 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0019 | 0/0 | 2395 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0020 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0021 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0022 | 0/0 | 2395 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0023 | 0/0 | 2395 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0024 | 0/0 | 2395 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0025 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0026 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0027 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0028 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0029 | 0/0 | 2395 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0030 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0031 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0032 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0033 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0034 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0035 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0036 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
t0037 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2856 | 128 | 24 | 24 | 60 | 7 | 13 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0001c0002 | 0/1 | 2856 | 82 | 23 | 11 | 38 | 4 | 5 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0001c0004 | 0/0 | 2856 | 6 | 6 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0001c0005 | 0/0 | 2856 | 4 | 4 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0001c0010 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0001c0011 | 1/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0001c0014 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0002c0003 | 0/0 | 2856 | 10 | 9 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0002c0012 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0003c0006 | 0/0 | 2856 | 3 | 2 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0004c0009 | 0/0 | 2856 | 2 | 0 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0005c0007 | 0/0 | 2856 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0006c0008 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 | |
a0007c0013 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5250 | 26 | 6 | 6 | 9 | 2 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0002 | 0/0 | 5250 | 29 | 0 | 7 | 20 | 1 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0003 | 0/0 | 5250 | 25 | 2 | 5 | 12 | 3 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0006 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0007 | 0/0 | 5250 | 13 | 4 | 3 | 4 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0009 | 0/0 | 5250 | 8 | 5 | 0 | 3 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0010 | 0/0 | 5250 | 4 | 2 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0012 | 0/0 | 5250 | 6 | 0 | 0 | 6 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0015 | 0/0 | 5250 | 3 | 0 | 0 | 3 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0016 | 0/0 | 5250 | 3 | 0 | 3 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0019 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0021 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0024 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0027 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0028 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0029 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0030 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0032 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0034 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0001t0036 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0001 | 0/0 | 5250 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0004 | 0/1 | 5250 | 23 | 2 | 4 | 13 | 2 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0005 | 0/0 | 5250 | 17 | 7 | 4 | 3 | 2 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0006 | 0/0 | 5250 | 9 | 7 | 0 | 2 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0008 | 0/0 | 5250 | 12 | 0 | 2 | 10 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0010 | 0/0 | 5250 | 2 | 1 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0011 | 0/0 | 5250 | 6 | 0 | 0 | 5 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0017 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0018 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0020 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0022 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0023 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0025 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0026 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0033 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0002t0037 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0004t0013 | 0/0 | 5250 | 5 | 5 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0004t0035 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0005t0014 | 0/0 | 5250 | 4 | 4 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0010t0007 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0011t0006 | 1/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0001c0014t0005 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0002c0003t0004 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0002c0003t0005 | 0/0 | 5250 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0002c0003t0006 | 0/0 | 5250 | 6 | 6 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0002c0003t0031 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0002c0012t0003 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0003c0006t0002 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0003c0006t0003 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0003c0006t0007 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0004c0009t0005 | 0/0 | 5250 | 2 | 0 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0005c0007t0001 | 0/0 | 5250 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0006c0008t0001 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0006c0008t0009 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
a0007c0013t0004 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | copy fasta | chr11 | 27360961 | 27477790 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0015g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0015g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0015g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0016g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0016g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0016g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0021g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0024g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0027g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0028g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0029g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0030g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0032g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0034g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0036g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0018g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0018g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0020g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0022g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0023g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0025g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0026g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0033g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0037g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0035g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0010t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0011t0006g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0014t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0031g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0012t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0003c0006t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0003c0006t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0003c0006t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0004c0009t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0004c0009t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0005c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0005c0007t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0006c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0006c0008t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0007c0013t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0029 | g0106 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00099 | hp2 | a0001 | c0002 | t0004 | g0135 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00408 | hp2 | a0001 | c0002 | t0008 | g0194 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00544 | hp1 | a0001 | c0002 | t0004 | g0073 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00544 | hp2 | a0001 | c0010 | t0007 | g0052 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00609 | hp2 | a0001 | c0001 | t0034 | g0205 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0062 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00735 | hp2 | a0001 | c0001 | t0016 | g0129 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00738 | hp1 | a0001 | c0002 | t0005 | g0050 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0113 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0049 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01109 | hp1 | a0002 | c0003 | t0005 | g0045 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0025 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01243 | hp2 | a0003 | c0006 | t0003 | g0140 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0071 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01257 | hp1 | a0005 | c0007 | t0001 | g0116 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01257 | hp2 | a0001 | c0002 | t0005 | g0026 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0061 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0072 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0001 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0069 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01517 | hp2 | a0001 | c0002 | t0005 | g0001 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01891 | hp1 | a0001 | c0002 | t0005 | g0033 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01943 | hp1 | a0001 | c0002 | t0004 | g0133 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01943 | hp2 | a0001 | c0002 | t0008 | g0195 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01975 | hp2 | a0001 | c0002 | t0008 | g0192 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01981 | hp2 | a0001 | c0001 | t0016 | g0112 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02004 | hp2 | a0001 | c0001 | t0007 | g0053 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02027 | hp2 | a0001 | c0002 | t0004 | g0121 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02055 | hp1 | a0002 | c0003 | t0006 | g0198 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02071 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02071 | hp2 | a0001 | c0002 | t0011 | g0077 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02074 | hp2 | a0001 | c0002 | t0004 | g0107 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02080 | hp1 | a0001 | c0002 | t0037 | g0242 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02080 | hp2 | a0001 | c0002 | t0008 | g0189 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02132 | hp1 | a0001 | c0002 | t0010 | g0047 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02135 | hp1 | a0001 | c0002 | t0006 | g0238 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02135 | hp2 | a0001 | c0001 | t0012 | g0084 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0221 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0151 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02148 | hp2 | a0001 | c0001 | t0016 | g0126 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02165 | hp1 | a0007 | c0013 | t0004 | g0063 | EAS | CDX | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02165 | hp2 | a0001 | c0002 | t0004 | g0088 | EAS | CDX | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02451 | hp2 | a0002 | c0003 | t0031 | g0180 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02572 | hp1 | a0001 | c0004 | t0013 | g0046 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02572 | hp2 | a0001 | c0002 | t0006 | g0233 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02615 | hp1 | a0002 | c0003 | t0006 | g0184 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02615 | hp2 | a0001 | c0005 | t0014 | g0150 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0174 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02622 | hp2 | a0001 | c0002 | t0018 | g0239 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02630 | hp1 | a0001 | c0002 | t0005 | g0007 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02630 | hp2 | a0001 | c0002 | t0018 | g0240 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02647 | hp1 | a0001 | c0005 | t0014 | g0149 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02683 | hp2 | a0004 | c0009 | t0005 | g0017 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02717 | hp1 | a0001 | c0002 | t0006 | g0200 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02717 | hp2 | a0003 | c0006 | t0002 | g0168 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02809 | hp1 | a0001 | c0002 | t0006 | g0187 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02809 | hp2 | a0003 | c0006 | t0007 | g0038 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02818 | hp1 | a0001 | c0001 | t0032 | g0175 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0219 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0010 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02896 | hp1 | a0001 | c0002 | t0017 | g0005 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02897 | hp1 | a0001 | c0002 | t0017 | g0006 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0012 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0183 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02970 | hp2 | a0001 | c0001 | t0030 | g0167 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02976 | hp1 | a0001 | c0004 | t0013 | g0042 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0177 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0022 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0008 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03139 | hp2 | a0002 | c0003 | t0006 | g0178 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03225 | hp1 | a0001 | c0002 | t0006 | g0186 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03225 | hp2 | a0006 | c0008 | t0009 | g0236 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03453 | hp1 | a0001 | c0005 | t0014 | g0155 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03453 | hp2 | a0001 | c0004 | t0013 | g0035 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03486 | hp1 | a0002 | c0003 | t0005 | g0032 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03486 | hp2 | a0006 | c0008 | t0001 | g0146 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03492 | hp1 | a0001 | c0001 | t0019 | g0003 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03540 | hp1 | a0002 | c0003 | t0006 | g0201 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03540 | hp2 | a0001 | c0004 | t0013 | g0013 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03579 | hp1 | a0001 | c0004 | t0013 | g0036 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03579 | hp2 | a0001 | c0002 | t0005 | g0011 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03654 | hp1 | a0001 | c0002 | t0023 | g0056 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0021 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03669 | hp2 | a0001 | c0002 | t0004 | g0074 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03834 | hp2 | a0001 | c0002 | t0022 | g0054 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04184 | hp1 | a0001 | c0001 | t0024 | g0125 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04184 | hp2 | a0001 | c0001 | t0010 | g0015 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04228 | hp1 | a0001 | c0001 | t0010 | g0058 | SAS | STU | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04228 | hp2 | a0004 | c0009 | t0005 | g0057 | SAS | STU | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18522 | hp1 | a0002 | c0012 | t0003 | g0156 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0179 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18612 | hp2 | a0001 | c0002 | t0008 | g0191 | EAS | CHB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18906 | hp1 | a0001 | c0001 | t0027 | g0138 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18906 | hp2 | a0002 | c0003 | t0004 | g0145 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18944 | hp1 | a0001 | c0001 | t0021 | g0028 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18944 | hp2 | a0001 | c0002 | t0008 | g0204 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18946 | hp2 | a0001 | c0002 | t0005 | g0024 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18950 | hp1 | a0001 | c0001 | t0009 | g0217 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18959 | hp1 | a0001 | c0002 | t0008 | g0170 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18960 | hp1 | a0001 | c0002 | t0033 | g0171 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18960 | hp2 | a0001 | c0001 | t0015 | g0030 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0086 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18964 | hp2 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18966 | hp2 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18967 | hp1 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18967 | hp2 | a0001 | c0002 | t0008 | g0196 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18975 | hp1 | a0001 | c0002 | t0004 | g0067 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18978 | hp1 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18982 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18982 | hp2 | a0001 | c0002 | t0011 | g0144 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18984 | hp1 | a0001 | c0002 | t0006 | g0225 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18985 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18985 | hp2 | a0001 | c0002 | t0011 | g0079 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18989 | hp1 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18990 | hp1 | a0001 | c0002 | t0011 | g0158 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18992 | hp2 | a0001 | c0002 | t0026 | g0120 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18993 | hp2 | a0001 | c0002 | t0008 | g0203 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18994 | hp1 | a0001 | c0002 | t0020 | g0004 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18994 | hp2 | a0001 | c0001 | t0028 | g0093 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0123 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0124 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19030 | hp1 | a0001 | c0002 | t0006 | g0199 | AFR | LWK | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | LWK | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19057 | hp1 | a0001 | c0002 | t0005 | g0023 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19058 | hp1 | a0001 | c0001 | t0012 | g0119 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19062 | hp1 | a0001 | c0002 | t0008 | g0228 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19068 | hp2 | a0001 | c0002 | t0011 | g0163 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19075 | hp1 | a0001 | c0002 | t0005 | g0044 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19076 | hp1 | a0001 | c0001 | t0015 | g0043 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19081 | hp1 | a0001 | c0002 | t0008 | g0190 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19082 | hp1 | a0001 | c0001 | t0012 | g0075 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19082 | hp2 | a0001 | c0002 | t0008 | g0237 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19085 | hp2 | a0001 | c0001 | t0015 | g0018 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19240 | hp1 | a0001 | c0002 | t0010 | g0009 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0141 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0065 | EUR | TSI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20752 | hp2 | a0001 | c0014 | t0005 | g0027 | EUR | TSI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20905 | hp1 | a0001 | c0002 | t0011 | g0091 | SAS | GIH | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0055 | SAS | GIH | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02109 | hp2 | a0002 | c0003 | t0006 | g0185 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02486 | hp1 | a0001 | c0002 | t0006 | g0197 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02486 | hp2 | a0001 | c0001 | t0036 | g0241 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02559 | hp1 | a0001 | c0002 | t0025 | g0092 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02559 | hp2 | a0001 | c0005 | t0014 | g0154 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03471 | hp1 | a0005 | c0007 | t0001 | g0096 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03471 | hp2 | a0001 | c0004 | t0035 | g0176 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG06807 | hp1 | a0001 | c0002 | t0005 | g0034 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20300 | hp1 | a0002 | c0003 | t0006 | g0207 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0004 | g0070 | REF | REF | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
homoSapiens_grch38 | hp1 | a0001 | c0011 | t0006 | g0181 | REF | REF | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27368475 | C | T | 1 | a0007 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2248G>A | p.Ala750Thr | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2736/5250 | 2248/2856 | 750/951 | chr11 | 27368475 | ||
chr11:27368597 | G | A | 2 | a0005a0006 | 4 | HG01257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.2126C>T | p.Thr709Met | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2614/5250 | 2126/2856 | 709/951 | chr11 | 27368597 | ||
chr11:27368673 | T | C | 1 | a0003 | 3 | HG01243.hp2 HG02717.hp2 HG02809.hp2 |
missense_variant | MODERATE | c.2050A>G | p.Arg684Gly | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2538/5250 | 2050/2856 | 684/951 | chr11 | 27368673 | ||
chr11:27372339 | G | A | 2 | a0002a0006 | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
missense_variant | MODERATE | c.1439C>T | p.Ala480Val | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 16/18 | 1927/5250 | 1439/2856 | 480/951 | chr11 | 27372339 | ||
chr11:27377180 | C | A | 1 | a0004 | 2 | HG02683.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.1087G>T | p.Gly363Cys | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/18 | 1575/5250 | 1087/2856 | 363/951 | chr11 | 27377180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27368134 | C | T | 1 | a0001c0014 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.2589G>A | p.Ser863Ser | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 3077/5250 | 2589/2856 | 863/951 | chr11 | 27368134 | ||
chr11:27368542 | T | C | 13 | a0001c0001a0001c0002a0001c0004others(10): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
synonymous_variant | LOW | c.2181A>G | p.Lys727Lys | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2669/5250 | 2181/2856 | 727/951 | chr11 | 27368542 | ||
chr11:27368620 | C | T | 1 | a0001c0010 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.2103G>A | p.Thr701Thr | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2591/5250 | 2103/2856 | 701/951 | chr11 | 27368620 | ||
chr11:27368929 | A | G | 1 | a0002c0003 | 10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.1794T>C | p.Asp598Asp | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2282/5250 | 1794/2856 | 598/951 | chr11 | 27368929 | ||
chr11:27368941 | T | C | 2 | a0001c0004a0001c0005 | 10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
synonymous_variant | LOW | c.1782A>G | p.Leu594Leu | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2270/5250 | 1782/2856 | 594/951 | chr11 | 27368941 | ||
chr11:27385297 | G | A | 5 | a0001c0002a0001c0005a0001c0014others(2): Show | 90 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(87): Show |
synonymous_variant | LOW | c.573C>T | p.Ser191Ser | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/18 | 1061/5250 | 573/2856 | 191/951 | chr11 | 27385297 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27366085 | G | A | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1782C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1782 | chr11 | 27366085 | |||||
chr11:27366106 | G | C | 1 | a0001c0001t0029 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1761C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1761 | chr11 | 27366106 | |||||
chr11:27366115 | C | A | 1 | a0001c0002t0033 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1752G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1752 | chr11 | 27366115 | |||||
chr11:27366144 | T | C | 2 | a0001c0001t0021a0001c0001t0028 | 2 | NA18944.hp1 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1723A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1723 | chr11 | 27366144 | |||||
chr11:27366468 | A | T | 1 | a0002c0003t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1399T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1399 | chr11 | 27366468 | |||||
chr11:27366633 | G | A | 1 | a0001c0001t0032 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1234 | chr11 | 27366633 | |||||
chr11:27366883 | C | T | 3 | a0001c0001t0012a0001c0001t0015a0001c0001t0034 | 10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*984G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 984 | chr11 | 27366883 | |||||
chr11:27366901 | C | T | 1 | a0001c0002t0026 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*966G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 966 | chr11 | 27366901 | |||||
chr11:27366907 | G | A | 1 | a0001c0001t0027 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 960 | chr11 | 27366907 | |||||
chr11:27366957 | G | A | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*910C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 910 | chr11 | 27366957 | |||||
chr11:27366984 | T | C | 4 | a0001c0002t0008a0001c0002t0011a0001c0002t0022others(1): Show | 20 | HG00408.hp2 HG01943.hp2 HG01975.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*883A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 883 | chr11 | 27366984 | |||||
chr11:27367077 | C | T | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(11): Show | 61 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*790G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 790 | chr11 | 27367077 | |||||
chr11:27367302 | C | G | 1 | a0001c0002t0025 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*565G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 565 | chr11 | 27367302 | |||||
chr11:27367363 | T | C | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(11): Show | 61 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 504 | chr11 | 27367363 | |||||
chr11:27367417 | T | C | 3 | a0001c0004t0013a0001c0004t0035a0001c0005t0014 | 10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 450 | chr11 | 27367417 | |||||
chr11:27367436 | G | A | 1 | a0001c0002t0023 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 431 | chr11 | 27367436 | |||||
chr11:27367839 | C | T | 1 | a0001c0001t0024 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 28 | chr11 | 27367839 | |||||
chr11:27367856 | C | T | 1 | a0001c0001t0016 | 3 | HG00735.hp2 HG01981.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 11 | chr11 | 27367856 | |||||
chr11:27472332 | C | G | 14 | a0001c0001t0007a0001c0001t0010a0001c0001t0015others(11): Show | 54 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-30G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 30 | chr11 | 27472332 | |||||
chr11:27472335 | G | A | 1 | a0001c0001t0030 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 33 | chr11 | 27472335 | |||||
chr11:27472423 | C | G | 1 | a0001c0002t0017 | 2 | HG02896.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 121 | chr11 | 27472423 | |||||
chr11:27472549 | C | G | 38 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(35): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-247G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | chr11 | 27472549 | ||||||
chr11:27472561 | C | A | 2 | a0001c0001t0036a0001c0002t0018 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-259G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | chr11 | 27472561 | ||||||
chr11:27472671 | C | G | 1 | a0001c0002t0020 | 1 | NA18994.hp1 | 5_prime_UTR_variant | MODIFIER | c.-369G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 369 | chr11 | 27472671 | |||||
chr11:27472673 | G | A | 1 | a0001c0002t0037 | 1 | HG02080.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-371C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | chr11 | 27472673 | ||||||
chr11:27472712 | C | T | 1 | a0001c0001t0019 | 1 | HG03492.hp1 | 5_prime_UTR_variant | MODIFIER | c.-410G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 410 | chr11 | 27472712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27369160 | C | G | 1 | a0001c0002t0006g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1580-17G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369160 | ||||||
chr11:27369240 | T | A | 2 | a0001c0001t0002g0208a0001c0001t0024g0125 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1580-97A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369240 | ||||||
chr11:27369903 | T | C | 61 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(58): Show | 61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1580-760A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369903 | ||||||
chr11:27369978 | T | C | 10 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0084others(7): Show | 10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1580-835A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369978 | ||||||
chr11:27370094 | G | T | 2 | a0001c0002t0005g0023a0001c0002t0005g0024 | 2 | NA18946.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1580-951C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370094 | ||||||
chr11:27370160 | T | G | 238 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1580-1017A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370160 | ||||||
chr11:27370323 | G | A | 6 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1180C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370323 | ||||||
chr11:27370327 | T | A | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1580-1184A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370327 | ||||||
chr11:27370414 | C | G | 2 | a0001c0002t0004g0113a0001c0002t0005g0026 | 2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1579+1201G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370414 | ||||||
chr11:27370642 | G | C | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+973C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370642 | ||||||
chr11:27370725 | C | G | 1 | a0003c0006t0003g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1579+890G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370725 | ||||||
chr11:27370751 | T | C | 1 | a0007c0013t0004g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1579+864A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370751 | ||||||
chr11:27370956 | T | C | 1 | a0001c0002t0005g0049 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1579+659A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370956 | ||||||
chr11:27370958 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1579+657G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370958 | ||||||
chr11:27371027 | T | C | 183 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0152others(180): Show | 185 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1579+588A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371027 | ||||||
chr11:27371369 | C | T | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0010g0009 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1579+246G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371369 | ||||||
chr11:27371370 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1579+245C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371370 | ||||||
chr11:27371486 | C | T | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1579+129G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371486 | ||||||
chr11:27372266 | G | A | 107 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(104): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1495+17C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 16/17 | chr11 | 27372266 | ||||||
chr11:27372448 | T | C | 6 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380-50A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372448 | ||||||
chr11:27372528 | G | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0137a0001c0001t0009g0216 | 3 | HG02071.hp1 NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1380-130C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372528 | ||||||
chr11:27372737 | C | T | 1 | a0002c0003t0006g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1380-339G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372737 | ||||||
chr11:27372868 | CT | C | 107 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(104): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1380-471delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372868 | ||||||
chr11:27372949 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1380-551A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372949 | ||||||
chr11:27373105 | C | A | 86 | a0001c0002t0004g0061a0001c0002t0004g0062a0001c0002t0004g0066others(83): Show | 87 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1379+446G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373105 | ||||||
chr11:27373154 | G | A | 86 | a0001c0002t0004g0061a0001c0002t0004g0062a0001c0002t0004g0066others(83): Show | 87 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1379+397C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373154 | ||||||
chr11:27373160 | C | T | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0010g0009 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1379+391G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373160 | ||||||
chr11:27373368 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1379+183A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373368 | ||||||
chr11:27373694 | C | G | 2 | a0003c0006t0002g0168a0003c0006t0007g0038 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1254-18G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373694 | ||||||
chr11:27373824 | G | A | 183 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0152others(180): Show | 185 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1254-148C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373824 | ||||||
chr11:27373830 | G | A | 86 | a0001c0002t0004g0061a0001c0002t0004g0062a0001c0002t0004g0066others(83): Show | 87 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1253+145C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373830 | ||||||
chr11:27373900 | C | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1253+75G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373900 | ||||||
chr11:27373924 | T | C | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0010g0009 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1253+51A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373924 | ||||||
chr11:27373940 | A | G | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0010g0009 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1253+35T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373940 | ||||||
chr11:27374328 | C | A | 110 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(107): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1182-282G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374328 | ||||||
chr11:27374338 | A | G | 1 | a0001c0001t0024g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1182-292T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374338 | ||||||
chr11:27374455 | C | T | 1 | a0001c0002t0004g0133 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1182-409G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374455 | ||||||
chr11:27374604 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1182-558C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374604 | ||||||
chr11:27374710 | A | C | 1 | a0001c0002t0004g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1182-664T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374710 | ||||||
chr11:27374756 | G | T | 238 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1182-710C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374756 | ||||||
chr11:27375077 | T | A | 238 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1182-1031A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375077 | ||||||
chr11:27375116 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1182-1070A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375116 | ||||||
chr11:27375121 | C | CA | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0002g0002others(10): Show | 14 | HG00140.hp2 HG00408.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1182-1076dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375121 | ||||||
chr11:27375194 | T | G | 2 | a0001c0002t0004g0076a0001c0002t0004g0086 | 2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1181+1105A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375194 | ||||||
chr11:27375263 | C | A | 8 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181+1036G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375263 | ||||||
chr11:27375297 | C | CA | 125 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1181+1001dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375297 | ||||||
chr11:27375297 | C | CAA | 9 | a0001c0001t0001g0127a0001c0001t0002g0188a0001c0001t0002g0193others(6): Show | 9 | HG01109.hp1 HG02027.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181+1000_1181+100 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375297 | ||||||
chr11:27375520 | A | G | 89 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(86): Show | 90 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1181+779T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375520 | ||||||
chr11:27375651 | C | T | 1 | a0001c0001t0029g0106 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1181+648G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375651 | ||||||
chr11:27375768 | C | T | 2 | a0001c0002t0004g0141a0001c0002t0005g0012 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1181+531G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375768 | ||||||
chr11:27375843 | G | A | 8 | a0001c0001t0002g0230a0001c0001t0003g0157a0001c0001t0003g0159others(5): Show | 8 | NA18951.hp1 NA18952.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1181+456C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375843 | ||||||
chr11:27375921 | TA | T | 85 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(82): Show | 86 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1181+377delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375921 | ||||||
chr11:27375977 | CT | C | 6 | a0001c0001t0003g0132a0001c0001t0003g0142a0001c0001t0007g0039others(3): Show | 6 | HG02451.hp1 HG06807.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+321delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375977 | ||||||
chr11:27375980 | T | C | 13 | a0002c0003t0004g0145a0002c0003t0005g0032a0002c0003t0005g0045others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+319A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375980 | ||||||
chr11:27376101 | C | T | 110 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(107): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1181+198G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376101 | ||||||
chr11:27376158 | T | TAG | 66 | a0001c0001t0001g0143a0001c0001t0001g0152a0001c0001t0001g0153others(63): Show | 66 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1181+139_1181+140d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376158 | ||||||
chr11:27376177 | C | T | 13 | a0002c0003t0004g0145a0002c0003t0005g0032a0002c0003t0005g0045others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+122G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376177 | ||||||
chr11:27376212 | G | A | 2 | a0003c0006t0002g0168a0003c0006t0007g0038 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1181+87C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376212 | ||||||
chr11:27376238 | A | G | 1 | a0001c0002t0004g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1181+61T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376238 | ||||||
chr11:27376247 | T | C | 1 | a0001c0002t0005g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1181+52A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376247 | ||||||
chr11:27376441 | G | T | 21 | a0001c0001t0003g0142a0001c0001t0007g0039a0001c0001t0007g0040others(18): Show | 21 | HG00609.hp2 HG01257.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110-71C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376441 | ||||||
chr11:27376468 | T | G | 12 | a0002c0003t0004g0145a0002c0003t0005g0032a0002c0003t0005g0045others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110-98A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376468 | ||||||
chr11:27376518 | T | C | 3 | a0001c0001t0016g0112a0001c0001t0016g0126a0001c0001t0016g0129 | 3 | HG00735.hp2 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1110-148A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376518 | ||||||
chr11:27376641 | G | T | 1 | a0001c0001t0036g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110-271C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376641 | ||||||
chr11:27376721 | C | A | 23 | a0001c0001t0001g0099a0001c0001t0003g0142a0001c0001t0007g0039others(20): Show | 23 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1110-351G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376721 | ||||||
chr11:27376724 | C | T | 31 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1110-354G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376724 | ||||||
chr11:27376768 | T | C | 3 | a0001c0001t0003g0142a0001c0001t0007g0039a0001c0001t0007g0040 | 3 | HG02451.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1109+390A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376768 | ||||||
chr11:27376953 | G | A | 2 | a0004c0009t0005g0017a0004c0009t0005g0057 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1109+205C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376953 | ||||||
chr11:27377007 | C | T | 1 | a0001c0001t0009g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1109+151G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27377007 | ||||||
chr11:27377097 | G | A | 6 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1109+61C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27377097 | ||||||
chr11:27377266 | A | C | 2 | a0003c0006t0002g0168a0003c0006t0007g0038 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1044-43T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377266 | ||||||
chr11:27377298 | G | A | 96 | a0001c0001t0001g0099a0001c0001t0001g0143a0001c0001t0001g0147others(93): Show | 96 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1044-75C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377298 | ||||||
chr11:27377524 | G | T | 237 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1044-301C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377524 | ||||||
chr11:27377559 | T | C | 10 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0084others(7): Show | 10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1044-336A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377559 | ||||||
chr11:27377721 | A | C | 1 | a0001c0002t0020g0004 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1044-498T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377721 | ||||||
chr11:27377866 | A | G | 31 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1044-643T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377866 | ||||||
chr11:27378019 | A | G | 62 | a0001c0001t0001g0143a0001c0001t0002g0188a0001c0001t0002g0193others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1043+678T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27378019 | ||||||
chr11:27378498 | T | C | 1 | a0001c0001t0003g0130 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1043+199A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27378498 | ||||||
chr11:27378545 | G | T | 1 | a0001c0002t0020g0004 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1043+152C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27378545 | ||||||
chr11:27379119 | G | A | 1 | a0001c0002t0005g0044 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.972-351C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379119 | ||||||
chr11:27379170 | C | T | 133 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.972-402G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379170 | ||||||
chr11:27379186 | T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.972-418A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379186 | ||||||
chr11:27379264 | A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.972-496T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379264 | ||||||
chr11:27379415 | C | T | 4 | a0001c0005t0014g0149a0001c0005t0014g0150a0001c0005t0014g0154others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-647G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379415 | ||||||
chr11:27379564 | C | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+707G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379564 | ||||||
chr11:27379622 | T | C | 237 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.971+649A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379622 | ||||||
chr11:27379643 | A | G | 68 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0152others(65): Show | 68 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.971+628T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379643 | ||||||
chr11:27379654 | G | A | 1 | a0001c0002t0005g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.971+617C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379654 | ||||||
chr11:27379779 | A | C | 1 | a0001c0001t0010g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.971+492T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379779 | ||||||
chr11:27379842 | C | T | 31 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.971+429G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379842 | ||||||
chr11:27379902 | TAAA | T | 141 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.971+366_971+368del others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379902 | ||||||
chr11:27380156 | G | A | 8 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(5): Show | 9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+115C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27380156 | ||||||
chr11:27380196 | A | T | 141 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.971+75T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27380196 | ||||||
chr11:27380380 | T | G | 89 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(86): Show | 90 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.903-41A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 9/17 | chr11 | 27380380 | ||||||
chr11:27380393 | T | A | 141 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.903-54A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 9/17 | chr11 | 27380393 | ||||||
chr11:27380833 | G | C | 12 | a0002c0003t0004g0145a0002c0003t0005g0032a0002c0003t0005g0045others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.830+62C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 8/17 | chr11 | 27380833 | ||||||
chr11:27380842 | C | T | 2 | a0004c0009t0005g0017a0004c0009t0005g0057 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.830+53G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 8/17 | chr11 | 27380842 | ||||||
chr11:27380866 | C | T | 1 | a0001c0004t0013g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.830+29G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 8/17 | chr11 | 27380866 | ||||||
chr11:27381035 | T | G | 22 | a0001c0001t0001g0099a0001c0001t0007g0039a0001c0001t0007g0040others(19): Show | 22 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.759-69A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381035 | ||||||
chr11:27381180 | A | G | 8 | a0001c0001t0009g0174a0001c0001t0009g0177a0001c0001t0009g0183others(5): Show | 8 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-214T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381180 | ||||||
chr11:27381363 | C | T | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.759-397G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381363 | ||||||
chr11:27381421 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.759-455T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381421 | ||||||
chr11:27381525 | T | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG00735.hp1 HG02004.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-559A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381525 | ||||||
chr11:27381589 | G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.758+599C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381589 | ||||||
chr11:27381649 | C | T | 88 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(85): Show | 89 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.758+539G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381649 | ||||||
chr11:27381706 | C | CA | 61 | a0001c0001t0001g0147a0001c0001t0002g0188a0001c0001t0002g0193others(58): Show | 61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.758+481dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381706 | ||||||
chr11:27381706 | CA | C | 169 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.758+481delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381706 | ||||||
chr11:27381734 | C | T | 13 | a0002c0003t0004g0145a0002c0003t0005g0032a0002c0003t0005g0045others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.758+454G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381734 | ||||||
chr11:27381785 | C | T | 61 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(58): Show | 61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.758+403G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381785 | ||||||
chr11:27382053 | T | C | 6 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+135A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27382053 | ||||||
chr11:27382279 | A | G | 1 | a0001c0002t0005g0010 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.690-23T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382279 | ||||||
chr11:27382332 | A | G | 2 | a0001c0002t0011g0091a0001c0002t0022g0054 | 2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.690-76T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382332 | ||||||
chr11:27382386 | C | T | 2 | a0001c0001t0001g0099a0001c0001t0009g0179 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.690-130G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382386 | ||||||
chr11:27382406 | G | A | 62 | a0001c0001t0001g0143a0001c0001t0002g0188a0001c0001t0002g0193others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.690-150C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382406 | ||||||
chr11:27382434 | AC | A | 31 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.690-179delG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382434 | ||||||
chr11:27382442 | GA | G | 3 | a0001c0001t0003g0142a0003c0006t0002g0168a0003c0006t0007g0038 | 3 | HG02717.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.690-187delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382442 | ||||||
chr11:27382704 | C | T | 1 | a0001c0005t0014g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690-448G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382704 | ||||||
chr11:27382869 | T | C | 3 | a0001c0001t0015g0018a0001c0001t0015g0030a0001c0001t0015g0043 | 3 | NA18960.hp2 NA19076.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.690-613A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382869 | ||||||
chr11:27382897 | G | T | 22 | a0001c0001t0001g0099a0001c0001t0007g0039a0001c0001t0007g0040others(19): Show | 22 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.690-641C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382897 | ||||||
chr11:27383010 | T | C | 238 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.690-754A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383010 | ||||||
chr11:27383222 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.690-966G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383222 | ||||||
chr11:27383309 | T | C | 85 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(82): Show | 86 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.689+1027A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383309 | ||||||
chr11:27383317 | G | T | 238 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.689+1019C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383317 | ||||||
chr11:27383330 | G | C | 89 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(86): Show | 90 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.689+1006C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383330 | ||||||
chr11:27383382 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.689+954C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383382 | ||||||
chr11:27383477 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.689+859G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383477 | ||||||
chr11:27383668 | T | G | 1 | a0001c0001t0002g0209 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.689+668A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383668 | ||||||
chr11:27383730 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.689+606C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383730 | ||||||
chr11:27383740 | G | A | 7 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(4): Show | 8 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+596C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383740 | ||||||
chr11:27383933 | G | A | 10 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0084others(7): Show | 10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.689+403C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383933 | ||||||
chr11:27384147 | C | T | 1 | a0001c0001t0030g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.689+189G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27384147 | ||||||
chr11:27384599 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.618-192C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384599 | ||||||
chr11:27384798 | C | G | 1 | a0001c0001t0009g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-391G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384798 | ||||||
chr11:27384866 | C | A | 1 | a0001c0001t0002g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.617+387G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384866 | ||||||
chr11:27384900 | C | T | 1 | a0001c0002t0006g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.617+353G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384900 | ||||||
chr11:27385531 | C | G | 1 | a0001c0001t0007g0019 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.402-63G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385531 | ||||||
chr11:27385736 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.402-268A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385736 | ||||||
chr11:27385815 | C | CA | 99 | a0001c0002t0001g0139a0001c0002t0004g0061a0001c0002t0004g0062others(96): Show | 100 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.402-348dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385815 | ||||||
chr11:27385815 | C | CAA | 110 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.402-349_402-348dup others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385815 | ||||||
chr11:27385815 | C | CAAA | 13 | a0001c0001t0003g0097a0001c0001t0007g0039a0001c0001t0007g0040others(10): Show | 13 | HG00609.hp2 HG01070.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.402-350_402-348dup others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385815 | ||||||
chr11:27385919 | A | G | 24 | a0001c0001t0001g0099a0001c0001t0007g0014a0001c0001t0007g0039others(21): Show | 24 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.402-451T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385919 | ||||||
chr11:27385980 | A | G | 87 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0061others(84): Show | 88 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.402-512T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385980 | ||||||
chr11:27386742 | CTGG | C | 6 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.402-1277_402-1275d others(5): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386742 | ||||||
chr11:27386870 | C | T | 145 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(142): Show | 146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.402-1402G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386870 | ||||||
chr11:27386922 | A | G | 1 | a0001c0010t0007g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.402-1454T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386922 | ||||||
chr11:27386938 | G | C | 7 | a0001c0001t0009g0174a0001c0001t0009g0177a0001c0001t0009g0183others(4): Show | 7 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.402-1470C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386938 | ||||||
chr11:27386967 | C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0122 | 2 | HG00639.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.402-1499G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386967 | ||||||
chr11:27387010 | C | G | 237 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.402-1542G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387010 | ||||||
chr11:27387042 | G | A | 2 | a0001c0002t0017g0005a0001c0002t0017g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.402-1574C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387042 | ||||||
chr11:27387139 | A | G | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.402-1671T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387139 | ||||||
chr11:27387317 | A | G | 12 | a0002c0003t0004g0145a0002c0003t0005g0032a0002c0003t0005g0045others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.402-1849T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387317 | ||||||
chr11:27387343 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.402-1875T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387343 | ||||||
chr11:27387417 | C | T | 231 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.402-1949G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387417 | ||||||
chr11:27387466 | T | TAAAGAAA others(341): Show |
1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.402-1999_402-1998i others(350): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387466 | ||||||
chr11:27387641 | A | T | 231 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.402-2173T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387641 | ||||||
chr11:27387945 | G | A | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.402-2477C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387945 | ||||||
chr11:27388036 | A | C | 1 | a0001c0001t0003g0160 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.402-2568T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388036 | ||||||
chr11:27388044 | T | C | 148 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0002g0188others(145): Show | 149 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.402-2576A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388044 | ||||||
chr11:27388079 | C | T | 63 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(60): Show | 63 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.402-2611G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388079 | ||||||
chr11:27388082 | A | G | 3 | a0001c0002t0006g0197a0001c0002t0018g0239a0001c0002t0018g0240 | 3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.402-2614T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388082 | ||||||
chr11:27388177 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.402-2709T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388177 | ||||||
chr11:27388349 | A | C | 237 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.401+2745T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388349 | ||||||
chr11:27388383 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.401+2711A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388383 | ||||||
chr11:27388452 | T | A | 1 | a0002c0003t0006g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.401+2642A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388452 | ||||||
chr11:27388824 | G | T | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401+2270C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388824 | ||||||
chr11:27389143 | A | G | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401+1951T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389143 | ||||||
chr11:27389389 | C | T | 3 | a0001c0002t0006g0197a0001c0002t0018g0239a0001c0002t0018g0240 | 3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.401+1705G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389389 | ||||||
chr11:27389408 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+1686A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389408 | ||||||
chr11:27389456 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.401+1638G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389456 | ||||||
chr11:27389507 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+1587G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389507 | ||||||
chr11:27389751 | G | A | 194 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.401+1343C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389751 | ||||||
chr11:27389799 | T | C | 1 | a0001c0002t0005g0025 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.401+1295A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389799 | ||||||
chr11:27390174 | TTA | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+918_401+919del others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390174 | ||||||
chr11:27390237 | G | A | 6 | a0001c0001t0001g0143a0001c0002t0006g0197a0001c0002t0018g0239others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+857C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390237 | ||||||
chr11:27390415 | G | A | 6 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(3): Show | 7 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.401+679C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390415 | ||||||
chr11:27390475 | T | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(3): Show | 7 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.401+619A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390475 | ||||||
chr11:27390735 | C | T | 2 | a0001c0001t0007g0014a0001c0001t0007g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.401+359G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390735 | ||||||
chr11:27390988 | C | T | 188 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.401+106G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390988 | ||||||
chr11:27391019 | T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.401+75A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27391019 | ||||||
chr11:27391235 | C | CTTTT | 5 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(2): Show | 6 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.330-74_330-71dupAA others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391235 | ||||||
chr11:27391235 | CTT | C | 195 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(192): Show | 196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.330-72_330-71delAA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391235 | ||||||
chr11:27391235 | CTTT | C | 34 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.330-73_330-71delAA others(1): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391235 | ||||||
chr11:27391307 | G | A | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0010g0009 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330-142C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391307 | ||||||
chr11:27391585 | C | G | 2 | a0001c0001t0006g0234a0001c0001t0030g0167 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.330-420G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391585 | ||||||
chr11:27391689 | GAAAT | G | 130 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(127): Show | 131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.330-528_330-525del others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391689 | ||||||
chr11:27391761 | T | C | 230 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.330-596A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391761 | ||||||
chr11:27391940 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.329+507G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391940 | ||||||
chr11:27392254 | GT | G | 8 | a0001c0001t0009g0174a0001c0001t0009g0177a0001c0001t0009g0183others(5): Show | 8 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.329+192delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27392254 | ||||||
chr11:27392308 | T | C | 237 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.329+139A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27392308 | ||||||
chr11:27392378 | C | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.329+69G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27392378 | ||||||
chr11:27392524 | GAA | G | 7 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(4): Show | 8 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.258-8_258-7delTT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27392524 | ||||||
chr11:27392661 | C | A | 6 | a0001c0001t0001g0143a0001c0002t0006g0197a0001c0002t0018g0239others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-143G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27392661 | ||||||
chr11:27393361 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-843A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393361 | ||||||
chr11:27393437 | T | G | 4 | a0001c0001t0006g0234a0001c0001t0027g0138a0001c0001t0030g0167others(1): Show | 4 | HG01243.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-919A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393437 | ||||||
chr11:27393503 | T | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(2): Show | 6 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-985A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393503 | ||||||
chr11:27393512 | CCT | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-996_258-995del others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393512 | ||||||
chr11:27393856 | T | C | 51 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.258-1338A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393856 | ||||||
chr11:27393937 | AT | A | 29 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0095others(26): Show | 29 | HG00099.hp1 HG00639.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.258-1420delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393937 | ||||||
chr11:27393938 | T | TG | 10 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(7): Show | 11 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.258-1421_258-1420i others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393938 | ||||||
chr11:27393938 | T | TGG | 3 | a0001c0001t0001g0099a0001c0001t0009g0179a0005c0007t0001g0096 | 3 | HG01891.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258-1421_258-1420i others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393938 | ||||||
chr11:27393938 | T | TGGGGG | 4 | a0001c0001t0009g0177a0001c0001t0009g0183a0001c0001t0009g0221others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1421_258-1420i others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393938 | ||||||
chr11:27393939 | T | G | 71 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0099others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.258-1421A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | ||||||
chr11:27393939 | T | TG | 33 | a0001c0001t0002g0202a0001c0001t0002g0208a0001c0001t0002g0220others(30): Show | 33 | HG00544.hp2 HG01169.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-1422dupC | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | ||||||
chr11:27393939 | T | TGG | 51 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0206others(48): Show | 51 | HG00544.hp1 HG00609.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.258-1423_258-1422d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | ||||||
chr11:27393939 | T | TGGG | 24 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0213others(21): Show | 24 | HG00408.hp1 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.258-1424_258-1422d others(5): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | ||||||
chr11:27393943 | G | A | 1 | a0002c0003t0031g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258-1425C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393943 | ||||||
chr11:27393943 | G | GC | 4 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0084others(1): Show | 4 | HG02135.hp2 NA18989.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-1426_258-1425i others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393943 | ||||||
chr11:27393944 | G | C | 6 | a0001c0001t0012g0118a0001c0001t0012g0119a0001c0001t0015g0018others(3): Show | 6 | HG00609.hp2 NA18960.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-1426C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393944 | ||||||
chr11:27393944 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-1426C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393944 | ||||||
chr11:27393945 | G | C | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.258-1427C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393945 | ||||||
chr11:27393949 | G | C | 38 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.258-1431C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393949 | ||||||
chr11:27393950 | G | A | 4 | a0001c0001t0006g0234a0001c0001t0027g0138a0001c0001t0030g0167others(1): Show | 4 | HG01243.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1432C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393950 | ||||||
chr11:27393955 | C | G | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.258-1437G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393955 | ||||||
chr11:27394063 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258-1545G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394063 | ||||||
chr11:27394064 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.258-1546C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394064 | ||||||
chr11:27394088 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.258-1570A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394088 | ||||||
chr11:27394381 | C | T | 7 | a0001c0002t0004g0076a0001c0002t0004g0086a0001c0002t0004g0087others(4): Show | 7 | HG02080.hp1 NA18964.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-1863G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394381 | ||||||
chr11:27394547 | C | T | 1 | a0003c0006t0003g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.258-2029G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394547 | ||||||
chr11:27394560 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.258-2042C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394560 | ||||||
chr11:27394592 | G | A | 19 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0210others(16): Show | 19 | HG00733.hp1 HG01975.hp1 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.258-2074C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394592 | ||||||
chr11:27394725 | A | G | 10 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0006g0234others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.258-2207T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394725 | ||||||
chr11:27395062 | T | C | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-2544A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395062 | ||||||
chr11:27395134 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.258-2616A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395134 | ||||||
chr11:27395166 | C | T | 10 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0084others(7): Show | 10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-2648G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395166 | ||||||
chr11:27395202 | G | C | 29 | a0001c0001t0001g0147a0001c0001t0002g0002a0001c0001t0002g0172others(26): Show | 30 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.258-2684C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395202 | ||||||
chr11:27395300 | A | G | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0004t0013g0013others(5): Show | 8 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-2782T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395300 | ||||||
chr11:27395354 | T | TA | 10 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0006g0234others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.258-2837dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395354 | ||||||
chr11:27395354 | TA | T | 9 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0006g0197others(6): Show | 9 | HG00642.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-2837delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395354 | ||||||
chr11:27395679 | T | C | 106 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(103): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.258-3161A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395679 | ||||||
chr11:27395746 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-3228G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395746 | ||||||
chr11:27395757 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-3239C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395757 | ||||||
chr11:27396087 | C | A | 1 | a0001c0002t0025g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.258-3569G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396087 | ||||||
chr11:27396088 | C | A | 1 | a0001c0002t0025g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.258-3570G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396088 | ||||||
chr11:27396149 | C | A | 73 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(70): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.258-3631G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396149 | ||||||
chr11:27396255 | C | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258-3737G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396255 | ||||||
chr11:27396403 | C | T | 1 | a0002c0003t0005g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.258-3885G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396403 | ||||||
chr11:27396536 | A | AT | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0004t0013g0013others(5): Show | 8 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-4019dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396536 | ||||||
chr11:27396539 | T | A | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0003g0082others(9): Show | 12 | HG00735.hp1 HG01243.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.258-4021A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396539 | ||||||
chr11:27396563 | G | A | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258-4045C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396563 | ||||||
chr11:27396678 | G | T | 73 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(70): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.258-4160C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396678 | ||||||
chr11:27397033 | C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0004t0013g0013others(5): Show | 8 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-4515G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397033 | ||||||
chr11:27397053 | A | G | 2 | a0006c0008t0001g0146a0006c0008t0009g0236 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.258-4535T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397053 | ||||||
chr11:27397083 | T | C | 3 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0085 | 3 | NA18989.hp1 NA19010.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.258-4565A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397083 | ||||||
chr11:27397254 | C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-4736G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397254 | ||||||
chr11:27397332 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.258-4814C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397332 | ||||||
chr11:27397444 | C | A | 28 | a0001c0001t0001g0147a0001c0001t0002g0002a0001c0001t0002g0172others(25): Show | 29 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-4926G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397444 | ||||||
chr11:27397510 | T | G | 1 | a0001c0002t0004g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.258-4992A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397510 | ||||||
chr11:27397587 | T | C | 91 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.258-5069A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397587 | ||||||
chr11:27397640 | G | C | 1 | a0001c0001t0002g0208 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.258-5122C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397640 | ||||||
chr11:27397673 | G | A | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0010g0009 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.258-5155C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397673 | ||||||
chr11:27397769 | C | G | 1 | a0001c0001t0003g0161 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.258-5251G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397769 | ||||||
chr11:27398205 | G | A | 4 | a0001c0001t0001g0099a0001c0001t0009g0179a0003c0006t0002g0168others(1): Show | 4 | HG01891.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-5687C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398205 | ||||||
chr11:27398235 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.258-5717C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398235 | ||||||
chr11:27398308 | T | C | 1 | a0001c0002t0008g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.258-5790A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398308 | ||||||
chr11:27398339 | A | G | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-5821T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398339 | ||||||
chr11:27398516 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258-5998G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398516 | ||||||
chr11:27398598 | G | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(15): Show | 19 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.258-6080C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398598 | ||||||
chr11:27398994 | C | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-6476G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398994 | ||||||
chr11:27399034 | C | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258-6516G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399034 | ||||||
chr11:27399059 | T | C | 144 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.258-6541A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399059 | ||||||
chr11:27399165 | C | A | 17 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0210others(14): Show | 17 | HG01975.hp1 HG02148.hp1 NA18971.hp1 others(14): Show |
intron_variant | MODIFIER | c.258-6647G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399165 | ||||||
chr11:27399262 | G | A | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-6744C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399262 | ||||||
chr11:27399581 | G | A | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-7063C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399581 | ||||||
chr11:27399615 | G | T | 3 | a0001c0001t0003g0108a0001c0001t0016g0112a0001c0001t0016g0126 | 3 | HG00733.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.258-7097C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399615 | ||||||
chr11:27400388 | G | A | 1 | a0001c0002t0004g0133 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.258-7870C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400388 | ||||||
chr11:27400523 | G | A | 1 | a0001c0001t0029g0106 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.258-8005C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400523 | ||||||
chr11:27400612 | C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-8094G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400612 | ||||||
chr11:27400725 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258-8207C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400725 | ||||||
chr11:27400799 | T | C | 1 | a0004c0009t0005g0017 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.258-8281A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400799 | ||||||
chr11:27400839 | G | A | 1 | a0001c0002t0005g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258-8321C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400839 | ||||||
chr11:27400906 | C | T | 6 | a0001c0001t0001g0099a0001c0001t0007g0014a0001c0001t0007g0039others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-8388G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400906 | ||||||
chr11:27400924 | T | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(19): Show | 23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-8406A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400924 | ||||||
chr11:27400983 | C | A | 1 | a0001c0005t0014g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.258-8465G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400983 | ||||||
chr11:27401043 | T | C | 1 | a0001c0001t0002g0229 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.258-8525A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401043 | ||||||
chr11:27401083 | A | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.258-8565T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401083 | ||||||
chr11:27401098 | T | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(18): Show | 22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-8580A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401098 | ||||||
chr11:27401106 | C | G | 21 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(18): Show | 22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-8588G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401106 | ||||||
chr11:27401118 | G | A | 1 | a0001c0002t0010g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.258-8600C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401118 | ||||||
chr11:27401159 | C | T | 113 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(110): Show | 115 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.258-8641G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401159 | ||||||
chr11:27401424 | C | T | 57 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0001t0001g0143others(54): Show | 58 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258-8906G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401424 | ||||||
chr11:27401539 | C | T | 55 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0007g0016others(52): Show | 56 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.258-9021G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401539 | ||||||
chr11:27401615 | T | C | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.258-9097A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401615 | ||||||
chr11:27401627 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258-9109A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401627 | ||||||
chr11:27401706 | A | C | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-9188T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401706 | ||||||
chr11:27401795 | C | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258-9277G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401795 | ||||||
chr11:27402076 | C | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258-9558G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402076 | ||||||
chr11:27402132 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-9614C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402132 | ||||||
chr11:27402220 | C | A | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-9702G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402220 | ||||||
chr11:27402339 | C | T | 1 | a0001c0001t0034g0205 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.258-9821G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402339 | ||||||
chr11:27402415 | TA | T | 106 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(103): Show | 108 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.258-9898delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402415 | ||||||
chr11:27402577 | C | T | 1 | a0001c0010t0007g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.258-10059G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402577 | ||||||
chr11:27402826 | G | A | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.257+9963C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402826 | ||||||
chr11:27402902 | A | G | 1 | a0001c0001t0030g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.257+9887T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402902 | ||||||
chr11:27403206 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.257+9583G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403206 | ||||||
chr11:27403320 | G | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+9469C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403320 | ||||||
chr11:27403731 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+9058G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403731 | ||||||
chr11:27403821 | T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0137a0001c0002t0004g0136 | 3 | NA18978.hp1 NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.257+8968A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403821 | ||||||
chr11:27403878 | T | C | 1 | a0001c0002t0006g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.257+8911A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403878 | ||||||
chr11:27403949 | G | A | 7 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(4): Show | 7 | NA18971.hp1 NA18984.hp2 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+8840C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403949 | ||||||
chr11:27404236 | C | T | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(10): Show | 13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+8553G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404236 | ||||||
chr11:27404293 | C | T | 1 | a0001c0004t0013g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.257+8496G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404293 | ||||||
chr11:27404485 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.257+8304A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404485 | ||||||
chr11:27404795 | TC | T | 114 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(111): Show | 116 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.257+7993delG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404795 | ||||||
chr11:27404844 | G | A | 144 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.257+7945C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404844 | ||||||
chr11:27404967 | T | G | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+7822A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404967 | ||||||
chr11:27405260 | C | T | 2 | a0001c0001t0001g0099a0001c0001t0009g0179 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.257+7529G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405260 | ||||||
chr11:27405474 | G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0098a0001c0001t0001g0137others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+7315C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405474 | ||||||
chr11:27405648 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+7141T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405648 | ||||||
chr11:27405949 | C | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+6840G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405949 | ||||||
chr11:27406123 | C | G | 1 | a0001c0001t0003g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.257+6666G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406123 | ||||||
chr11:27406241 | C | G | 2 | a0002c0003t0005g0032a0002c0003t0006g0178 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.257+6548G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406241 | ||||||
chr11:27406330 | C | T | 1 | a0001c0001t0007g0016 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.257+6459G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406330 | ||||||
chr11:27406349 | C | T | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+6440G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406349 | ||||||
chr11:27406481 | G | A | 1 | a0001c0002t0004g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.257+6308C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406481 | ||||||
chr11:27406717 | C | A | 32 | a0001c0001t0001g0090a0001c0001t0007g0016a0001c0002t0004g0061others(29): Show | 33 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.257+6072G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406717 | ||||||
chr11:27406956 | C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+5833G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406956 | ||||||
chr11:27407208 | G | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+5581C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407208 | ||||||
chr11:27407587 | A | C | 1 | a0002c0003t0005g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.257+5202T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407587 | ||||||
chr11:27407670 | TA | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+5118delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407670 | ||||||
chr11:27407979 | A | C | 1 | a0001c0001t0002g0218 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.257+4810T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407979 | ||||||
chr11:27408273 | T | C | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+4516A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408273 | ||||||
chr11:27408392 | T | C | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+4397A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408392 | ||||||
chr11:27408439 | C | T | 56 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0007g0016others(53): Show | 57 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.257+4350G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408439 | ||||||
chr11:27408867 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+3922G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408867 | ||||||
chr11:27409057 | A | C | 1 | a0001c0001t0003g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.257+3732T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409057 | ||||||
chr11:27409197 | C | G | 1 | a0001c0001t0010g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.257+3592G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409197 | ||||||
chr11:27409573 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+3216G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409573 | ||||||
chr11:27409619 | T | C | 2 | a0001c0001t0007g0029a0001c0001t0010g0048 | 2 | HG01099.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.257+3170A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409619 | ||||||
chr11:27409732 | A | C | 4 | a0001c0001t0032g0175a0002c0012t0003g0156a0003c0006t0002g0168others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+3057T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409732 | ||||||
chr11:27409843 | C | T | 96 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0001t0001g0114others(93): Show | 98 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.257+2946G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409843 | ||||||
chr11:27410130 | C | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+2659G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410130 | ||||||
chr11:27410159 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.257+2630C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410159 | ||||||
chr11:27410204 | G | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+2585C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410204 | ||||||
chr11:27410212 | C | T | 1 | a0001c0005t0014g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.257+2577G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410212 | ||||||
chr11:27410249 | G | C | 14 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.257+2540C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410249 | ||||||
chr11:27410706 | A | G | 2 | a0001c0001t0001g0099a0001c0001t0009g0179 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.257+2083T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410706 | ||||||
chr11:27410711 | T | G | 17 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0210others(14): Show | 17 | HG01975.hp1 HG02148.hp1 NA18971.hp1 others(14): Show |
intron_variant | MODIFIER | c.257+2078A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410711 | ||||||
chr11:27410796 | T | C | 1 | a0005c0007t0001g0116 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.257+1993A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410796 | ||||||
chr11:27411332 | T | C | 55 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0007g0016others(52): Show | 56 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.257+1457A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27411332 | ||||||
chr11:27411949 | T | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+840A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27411949 | ||||||
chr11:27412039 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+750G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412039 | ||||||
chr11:27412285 | A | G | 113 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(110): Show | 115 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.257+504T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412285 | ||||||
chr11:27412306 | C | G | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+483G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412306 | ||||||
chr11:27412473 | C | T | 1 | a0002c0003t0006g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.257+316G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412473 | ||||||
chr11:27412870 | G | A | 1 | a0001c0002t0004g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.186-10C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27412870 | ||||||
chr11:27413359 | T | C | 18 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0210others(15): Show | 18 | HG01975.hp1 HG02148.hp1 NA18950.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-499A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413359 | ||||||
chr11:27413544 | G | A | 1 | a0001c0001t0010g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-684C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413544 | ||||||
chr11:27413612 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-752C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413612 | ||||||
chr11:27413651 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.186-791C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413651 | ||||||
chr11:27413740 | T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-880A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413740 | ||||||
chr11:27413748 | G | A | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186-888C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413748 | ||||||
chr11:27413750 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.186-890G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413750 | ||||||
chr11:27413945 | T | G | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-1085A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413945 | ||||||
chr11:27414375 | T | C | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-1515A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414375 | ||||||
chr11:27414376 | T | A | 1 | a0001c0001t0012g0118 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.186-1516A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414376 | ||||||
chr11:27414396 | T | TA | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0006g0234others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-1537dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414396 | ||||||
chr11:27414396 | TA | T | 22 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(19): Show | 23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-1537delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414396 | ||||||
chr11:27414584 | G | A | 114 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(111): Show | 116 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.186-1724C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414584 | ||||||
chr11:27414586 | G | A | 114 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(111): Show | 116 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.186-1726C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414586 | ||||||
chr11:27414759 | CAGAAA | C | 55 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0007g0016others(52): Show | 56 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.186-1904_186-1900d others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414759 | ||||||
chr11:27414766 | G | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-1906C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414766 | ||||||
chr11:27414771 | G | A | 4 | a0001c0001t0009g0174a0001c0001t0009g0177a0001c0001t0009g0183others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-1911C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414771 | ||||||
chr11:27414809 | G | C | 84 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(81): Show | 85 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.186-1949C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414809 | ||||||
chr11:27414810 | T | C | 7 | a0001c0001t0012g0075a0001c0001t0012g0081a0001c0001t0012g0084others(4): Show | 7 | HG00609.hp2 HG02135.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-1950A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414810 | ||||||
chr11:27414887 | C | T | 2 | a0001c0001t0001g0099a0001c0001t0009g0179 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-2027G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414887 | ||||||
chr11:27414940 | G | A | 1 | a0001c0004t0013g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-2080C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414940 | ||||||
chr11:27415342 | C | T | 2 | a0001c0001t0001g0099a0001c0001t0009g0179 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-2482G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415342 | ||||||
chr11:27415416 | C | T | 1 | a0001c0001t0010g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-2556G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415416 | ||||||
chr11:27415490 | G | T | 1 | a0001c0001t0003g0159 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.186-2630C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415490 | ||||||
chr11:27415499 | C | T | 1 | a0001c0002t0006g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-2639G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415499 | ||||||
chr11:27415651 | C | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.186-2791G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415651 | ||||||
chr11:27415809 | G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-2949C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415809 | ||||||
chr11:27416056 | T | C | 1 | a0001c0001t0003g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.186-3196A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416056 | ||||||
chr11:27416154 | A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0005c0007t0001g0096others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-3294T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416154 | ||||||
chr11:27416246 | G | A | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(10): Show | 13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-3386C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416246 | ||||||
chr11:27416254 | G | A | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186-3394C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416254 | ||||||
chr11:27416281 | T | C | 1 | a0001c0001t0010g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-3421A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416281 | ||||||
chr11:27416361 | A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-3501T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416361 | ||||||
chr11:27416544 | T | A | 32 | a0001c0001t0001g0090a0001c0001t0007g0016a0001c0002t0004g0061others(29): Show | 33 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-3684A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416544 | ||||||
chr11:27416950 | A | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-4090T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416950 | ||||||
chr11:27417076 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186-4216C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417076 | ||||||
chr11:27417205 | T | C | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-4345A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417205 | ||||||
chr11:27417504 | T | C | 1 | a0001c0002t0037g0242 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.186-4644A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417504 | ||||||
chr11:27417972 | C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0005c0007t0001g0096others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-5112G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417972 | ||||||
chr11:27418091 | C | A | 2 | a0001c0001t0007g0055a0001c0002t0022g0054 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.186-5231G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418091 | ||||||
chr11:27418091 | C | G | 1 | a0001c0002t0011g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.186-5231G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418091 | ||||||
chr11:27418127 | T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-5267A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418127 | ||||||
chr11:27418138 | T | A | 1 | a0001c0002t0004g0074 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.186-5278A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418138 | ||||||
chr11:27418168 | T | G | 2 | a0001c0001t0001g0099a0001c0001t0009g0179 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-5308A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418168 | ||||||
chr11:27418412 | G | A | 20 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0009g0216others(17): Show | 20 | HG00408.hp2 HG01943.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.186-5552C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418412 | ||||||
chr11:27418486 | G | C | 1 | a0001c0001t0007g0016 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.186-5626C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418486 | ||||||
chr11:27418736 | T | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0111 | 3 | NA18951.hp2 NA18952.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.186-5876A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418736 | ||||||
chr11:27418825 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186-5965A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418825 | ||||||
chr11:27418832 | CT | C | 48 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0115others(45): Show | 49 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.186-5973delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418832 | ||||||
chr11:27418832 | CTT | C | 37 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0143others(34): Show | 37 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.186-5974_186-5973d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418832 | ||||||
chr11:27418851 | G | T | 1 | a0001c0002t0006g0200 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-5991C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418851 | ||||||
chr11:27418853 | G | A | 1 | a0001c0002t0006g0200 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-5993C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418853 | ||||||
chr11:27419025 | A | T | 1 | a0001c0001t0002g0230 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.186-6165T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419025 | ||||||
chr11:27419258 | T | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-6398A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419258 | ||||||
chr11:27419274 | C | A | 14 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-6414G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419274 | ||||||
chr11:27419393 | T | G | 1 | a0001c0001t0003g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.186-6533A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419393 | ||||||
chr11:27419580 | T | TTA | 144 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.186-6722_186-6721d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419580 | ||||||
chr11:27419721 | T | C | 1 | a0001c0001t0003g0130 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186-6861A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419721 | ||||||
chr11:27419849 | C | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-6989G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419849 | ||||||
chr11:27420627 | C | T | 1 | a0004c0009t0005g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.186-7767G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27420627 | ||||||
chr11:27420785 | C | T | 24 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(21): Show | 25 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.186-7925G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27420785 | ||||||
chr11:27420838 | A | C | 6 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(3): Show | 6 | NA18971.hp1 NA18984.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-7978T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27420838 | ||||||
chr11:27421257 | C | T | 4 | a0001c0001t0032g0175a0002c0012t0003g0156a0003c0006t0002g0168others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-8397G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421257 | ||||||
chr11:27421517 | G | T | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-8657C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421517 | ||||||
chr11:27421604 | T | C | 115 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(112): Show | 117 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.186-8744A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421604 | ||||||
chr11:27421629 | A | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.186-8769T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421629 | ||||||
chr11:27421665 | C | T | 1 | a0001c0002t0010g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186-8805G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421665 | ||||||
chr11:27421714 | C | A | 2 | a0001c0001t0007g0014a0001c0001t0007g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.186-8854G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421714 | ||||||
chr11:27421852 | T | C | 2 | a0001c0001t0001g0137a0001c0002t0004g0136 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.186-8992A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421852 | ||||||
chr11:27421968 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.186-9108A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421968 | ||||||
chr11:27421970 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.186-9110T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421970 | ||||||
chr11:27421973 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.186-9113C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421973 | ||||||
chr11:27421994 | GT | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-9135delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421994 | ||||||
chr11:27422159 | G | A | 2 | a0001c0002t0017g0005a0001c0002t0017g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-9299C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422159 | ||||||
chr11:27422283 | T | C | 2 | a0001c0001t0001g0109a0001c0001t0009g0169 | 2 | HG02004.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.186-9423A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422283 | ||||||
chr11:27422471 | G | T | 1 | a0002c0003t0005g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.186-9611C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422471 | ||||||
chr11:27422608 | C | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-9748G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422608 | ||||||
chr11:27422628 | C | T | 60 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(57): Show | 61 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.186-9768G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422628 | ||||||
chr11:27422889 | C | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-10029G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422889 | ||||||
chr11:27422970 | T | C | 54 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0007g0016others(51): Show | 55 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.186-10110A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422970 | ||||||
chr11:27423039 | A | G | 1 | a0001c0002t0004g0074 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.186-10179T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423039 | ||||||
chr11:27423071 | T | C | 1 | a0001c0001t0003g0159 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.186-10211A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423071 | ||||||
chr11:27423461 | CCTT | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(2): Show | 6 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-10604_186-1060 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423461 | ||||||
chr11:27423583 | T | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(18): Show | 22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-10723A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423583 | ||||||
chr11:27423621 | A | G | 60 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(57): Show | 61 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.186-10761T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423621 | ||||||
chr11:27423966 | A | T | 1 | a0001c0001t0016g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.186-11106T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423966 | ||||||
chr11:27424118 | A | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-11258T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424118 | ||||||
chr11:27424292 | T | C | 1 | a0005c0007t0001g0116 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.186-11432A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424292 | ||||||
chr11:27424298 | G | A | 1 | a0001c0001t0003g0161 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.186-11438C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424298 | ||||||
chr11:27424305 | C | T | 2 | a0001c0001t0007g0029a0001c0001t0010g0048 | 2 | HG01099.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.186-11445G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424305 | ||||||
chr11:27424507 | C | A | 60 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(57): Show | 61 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.186-11647G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424507 | ||||||
chr11:27424705 | A | G | 1 | a0001c0001t0010g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-11845T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424705 | ||||||
chr11:27424732 | T | G | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-11872A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424732 | ||||||
chr11:27424844 | T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-11984A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424844 | ||||||
chr11:27424895 | G | A | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-12035C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424895 | ||||||
chr11:27425079 | C | G | 1 | a0001c0010t0007g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.186-12219G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425079 | ||||||
chr11:27425124 | G | C | 6 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(3): Show | 6 | HG02027.hp1 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-12264C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425124 | ||||||
chr11:27425326 | G | GTT | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(10): Show | 13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-12468_186-1246 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425326 | ||||||
chr11:27425329 | T | A | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-12469A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425329 | ||||||
chr11:27425338 | G | GTT | 21 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(18): Show | 22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-12480_186-1247 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425338 | ||||||
chr11:27425803 | C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0005c0007t0001g0096others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-12943G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425803 | ||||||
chr11:27425828 | T | A | 1 | a0001c0001t0030g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.186-12968A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425828 | ||||||
chr11:27425983 | G | T | 1 | a0001c0001t0009g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.186-13123C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425983 | ||||||
chr11:27425999 | T | C | 3 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141 | 3 | HG00642.hp2 HG02896.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.186-13139A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425999 | ||||||
chr11:27426128 | T | C | 1 | a0001c0002t0004g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.186-13268A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426128 | ||||||
chr11:27426295 | T | C | 1 | a0001c0001t0007g0016 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.186-13435A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426295 | ||||||
chr11:27426343 | T | C | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-13483A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426343 | ||||||
chr11:27426478 | C | T | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-13618G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426478 | ||||||
chr11:27426613 | T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0005c0007t0001g0096others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-13753A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426613 | ||||||
chr11:27426736 | C | G | 1 | a0001c0002t0008g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.186-13876G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426736 | ||||||
chr11:27426788 | A | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-13928T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426788 | ||||||
chr11:27426862 | G | A | 22 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(19): Show | 23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-14002C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426862 | ||||||
chr11:27427097 | G | C | 1 | a0001c0002t0010g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186-14237C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427097 | ||||||
chr11:27427104 | G | A | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-14244C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427104 | ||||||
chr11:27427258 | C | T | 1 | a0001c0001t0007g0016 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.186-14398G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427258 | ||||||
chr11:27427363 | G | A | 3 | a0001c0001t0007g0055a0001c0001t0019g0003a0001c0002t0022g0054 | 3 | HG03492.hp1 HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.186-14503C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427363 | ||||||
chr11:27427380 | G | A | 1 | a0002c0003t0031g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186-14520C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427380 | ||||||
chr11:27427450 | A | G | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14590T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427450 | ||||||
chr11:27427452 | C | A | 1 | a0001c0002t0025g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186-14592G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427452 | ||||||
chr11:27427521 | C | A | 29 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0100others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.186-14661G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427521 | ||||||
chr11:27427664 | C | T | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14804G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427664 | ||||||
chr11:27427688 | A | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-14828T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427688 | ||||||
chr11:27427798 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-14938C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427798 | ||||||
chr11:27427805 | C | T | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14945G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427805 | ||||||
chr11:27427814 | G | A | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14954C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427814 | ||||||
chr11:27427823 | A | G | 1 | a0001c0002t0004g0071 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.186-14963T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427823 | ||||||
chr11:27427862 | G | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-15002C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427862 | ||||||
chr11:27427922 | C | T | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-15062G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427922 | ||||||
chr11:27427998 | G | A | 1 | a0001c0001t0010g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-15138C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427998 | ||||||
chr11:27428139 | C | CT | 22 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(19): Show | 23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-15280dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428139 | ||||||
chr11:27428139 | CT | C | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-15280delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428139 | ||||||
chr11:27428223 | T | C | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-15363A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428223 | ||||||
chr11:27428287 | C | T | 44 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0114others(41): Show | 45 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.186-15427G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428287 | ||||||
chr11:27428362 | T | C | 61 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(58): Show | 62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-15502A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428362 | ||||||
chr11:27428432 | C | T | 3 | a0001c0001t0001g0099a0001c0001t0009g0179a0001c0002t0004g0062 | 3 | HG00639.hp1 HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-15572G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428432 | ||||||
chr11:27428492 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-15632C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428492 | ||||||
chr11:27428500 | T | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(19): Show | 23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-15640A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428500 | ||||||
chr11:27428619 | T | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(10): Show | 13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-15759A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428619 | ||||||
chr11:27428636 | C | CTAGATAG others(2): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0115a0005c0007t0001g0096others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-15777_186-1577 others(13): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428636 | ||||||
chr11:27428640 | A | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0005c0007t0001g0096others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-15780T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428640 | ||||||
chr11:27428749 | T | G | 1 | a0001c0002t0004g0107 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.186-15889A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428749 | ||||||
chr11:27428763 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.186-15903G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428763 | ||||||
chr11:27428818 | G | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-15958C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428818 | ||||||
chr11:27428855 | C | T | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186-15995G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428855 | ||||||
chr11:27428984 | A | G | 116 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(113): Show | 118 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.186-16124T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428984 | ||||||
chr11:27429217 | G | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-16357C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429217 | ||||||
chr11:27429254 | G | A | 2 | a0006c0008t0001g0146a0006c0008t0009g0236 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.186-16394C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429254 | ||||||
chr11:27429343 | G | A | 26 | a0001c0001t0001g0143a0001c0001t0006g0234a0001c0001t0012g0075others(23): Show | 26 | HG00609.hp2 HG00642.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.186-16483C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429343 | ||||||
chr11:27429470 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186-16610C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429470 | ||||||
chr11:27429482 | C | CA | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0007g0014others(8): Show | 11 | HG00735.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-16623dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429482 | ||||||
chr11:27429499 | A | C | 3 | a0001c0001t0032g0175a0003c0006t0002g0168a0003c0006t0007g0038 | 3 | HG02717.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.186-16639T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429499 | ||||||
chr11:27429514 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186-16654C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429514 | ||||||
chr11:27429518 | G | A | 1 | a0001c0001t0009g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.186-16658C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429518 | ||||||
chr11:27429686 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.186-16826T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429686 | ||||||
chr11:27430015 | G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-17155C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430015 | ||||||
chr11:27430167 | C | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(3): Show | 7 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-17307G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430167 | ||||||
chr11:27430212 | C | A | 62 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0099others(59): Show | 63 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.186-17352G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430212 | ||||||
chr11:27430405 | GA | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(2): Show | 5 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-17546delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430405 | ||||||
chr11:27430478 | A | G | 4 | a0001c0001t0002g0208a0001c0001t0007g0055a0001c0001t0019g0003others(1): Show | 4 | HG02698.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-17618T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430478 | ||||||
chr11:27430879 | C | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0005t0014g0149others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-18019G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430879 | ||||||
chr11:27430913 | A | C | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-18053T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430913 | ||||||
chr11:27431011 | G | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0172a0001c0001t0002g0173others(18): Show | 22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-18151C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431011 | ||||||
chr11:27431159 | A | G | 6 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(3): Show | 6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-18299T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431159 | ||||||
chr11:27431387 | C | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-18527G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431387 | ||||||
chr11:27431583 | C | T | 1 | a0001c0001t0007g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.186-18723G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431583 | ||||||
chr11:27431584 | G | A | 3 | a0001c0002t0006g0197a0001c0002t0018g0239a0001c0002t0018g0240 | 3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.186-18724C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431584 | ||||||
chr11:27431587 | C | T | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-18727G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431587 | ||||||
chr11:27431772 | T | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0032g0175others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-18912A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431772 | ||||||
chr11:27431866 | T | C | 5 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-19006A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431866 | ||||||
chr11:27432032 | C | T | 3 | a0001c0001t0027g0138a0001c0001t0030g0167a0003c0006t0003g0140 | 3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-19172G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432032 | ||||||
chr11:27432196 | A | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0235 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.186-19336T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432196 | ||||||
chr11:27432205 | A | C | 20 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0012g0075others(17): Show | 20 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.186-19345T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432205 | ||||||
chr11:27432374 | G | A | 2 | a0001c0005t0014g0149a0001c0005t0014g0154 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.186-19514C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432374 | ||||||
chr11:27432545 | A | C | 5 | a0001c0004t0013g0013a0001c0004t0013g0035a0001c0004t0013g0036others(2): Show | 5 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-19685T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432545 | ||||||
chr11:27432668 | C | G | 4 | a0001c0001t0009g0179a0001c0002t0004g0062a0001c0002t0004g0151others(1): Show | 4 | HG00639.hp1 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-19808G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432668 | ||||||
chr11:27432680 | C | T | 241 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.186-19820G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432680 | ||||||
chr11:27433222 | T | C | 8 | a0001c0001t0006g0234a0001c0001t0010g0037a0001c0002t0004g0062others(5): Show | 8 | HG00639.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-20362A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433222 | ||||||
chr11:27433252 | A | G | 241 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.186-20392T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433252 | ||||||
chr11:27433312 | T | A | 1 | a0001c0002t0020g0004 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-20452A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433312 | ||||||
chr11:27433341 | T | C | 1 | a0001c0001t0003g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.186-20481A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433341 | ||||||
chr11:27433387 | A | C | 1 | a0001c0001t0003g0160 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.186-20527T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433387 | ||||||
chr11:27433397 | CT | C | 164 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(161): Show | 165 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.186-20538delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433397 | ||||||
chr11:27433615 | T | C | 6 | a0001c0001t0010g0037a0001c0004t0013g0013a0001c0004t0013g0035others(3): Show | 6 | HG02572.hp1 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-20755A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433615 | ||||||
chr11:27433946 | A | G | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-21086T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433946 | ||||||
chr11:27433950 | T | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-21090A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433950 | ||||||
chr11:27434029 | T | C | 223 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.186-21169A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434029 | ||||||
chr11:27434035 | C | T | 167 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(164): Show | 168 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.186-21175G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434035 | ||||||
chr11:27434321 | T | G | 1 | a0001c0002t0006g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186-21461A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434321 | ||||||
chr11:27434512 | C | T | 167 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(164): Show | 168 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.186-21652G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434512 | ||||||
chr11:27434887 | T | C | 3 | a0001c0001t0009g0179a0001c0002t0004g0062a0001c0004t0035g0176 | 3 | HG00639.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-22027A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434887 | ||||||
chr11:27434941 | T | C | 167 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(164): Show | 168 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.186-22081A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434941 | ||||||
chr11:27435129 | G | A | 9 | a0001c0001t0032g0175a0001c0002t0005g0007a0001c0002t0005g0008others(6): Show | 9 | HG01891.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-22269C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435129 | ||||||
chr11:27435205 | C | T | 28 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(25): Show | 28 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.186-22345G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435205 | ||||||
chr11:27435287 | T | G | 2 | a0001c0001t0001g0147a0001c0001t0003g0142 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.186-22427A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435287 | ||||||
chr11:27435348 | AAAC | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-22491_186-2248 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435348 | ||||||
chr11:27435415 | A | G | 2 | a0001c0001t0001g0143a0003c0006t0002g0168 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.186-22555T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435415 | ||||||
chr11:27435488 | G | A | 33 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(30): Show | 33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-22628C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435488 | ||||||
chr11:27435512 | A | G | 33 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(30): Show | 33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-22652T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435512 | ||||||
chr11:27435548 | T | G | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.186-22688A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435548 | ||||||
chr11:27435581 | G | A | 6 | a0001c0002t0004g0135a0001c0002t0005g0001a0001c0002t0005g0025others(3): Show | 7 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-22721C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435581 | ||||||
chr11:27435646 | C | T | 33 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(30): Show | 33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-22786G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435646 | ||||||
chr11:27435774 | A | C | 167 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(164): Show | 168 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.186-22914T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435774 | ||||||
chr11:27435933 | C | T | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-23073G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435933 | ||||||
chr11:27435965 | C | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-23105G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435965 | ||||||
chr11:27436037 | GAGTTGCT others(8): Show |
G | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(6): Show | 9 | HG02572.hp1 HG02647.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-23192_186-2317 others(19): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436037 | ||||||
chr11:27436057 | G | A | 21 | a0001c0001t0007g0014a0001c0001t0007g0019a0001c0001t0007g0039others(18): Show | 21 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.186-23197C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436057 | ||||||
chr11:27436113 | G | A | 28 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(25): Show | 28 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.186-23253C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436113 | ||||||
chr11:27436204 | C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0003g0134others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-23344G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436204 | ||||||
chr11:27436206 | T | G | 1 | a0001c0001t0007g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-23346A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436206 | ||||||
chr11:27436293 | G | A | 1 | a0001c0002t0005g0010 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.186-23433C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436293 | ||||||
chr11:27436302 | C | T | 29 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(26): Show | 29 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(26): Show |
intron_variant | MODIFIER | c.186-23442G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436302 | ||||||
chr11:27436347 | G | GAGAA | 67 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(64): Show | 67 | HG00735.hp2 HG01070.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.186-23491_186-2348 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436347 | ||||||
chr11:27436347 | GAGAA | G | 29 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0007g0014others(26): Show | 29 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.186-23491_186-2348 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436347 | ||||||
chr11:27436371 | AAGAG | A | 7 | a0001c0001t0001g0143a0001c0001t0030g0167a0001c0002t0017g0005others(4): Show | 7 | HG02717.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-23515_186-2351 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436371 | ||||||
chr11:27436373 | G | GAA | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0010g0037others(5): Show | 8 | HG02572.hp1 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-23514_186-2351 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436373 | ||||||
chr11:27436602 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186-23742A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436602 | ||||||
chr11:27436674 | T | C | 6 | a0001c0001t0007g0019a0001c0001t0015g0018a0001c0001t0015g0030others(3): Show | 6 | NA18946.hp2 NA18960.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-23814A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436674 | ||||||
chr11:27436750 | A | G | 1 | a0001c0002t0005g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.186-23890T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436750 | ||||||
chr11:27436863 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.186-24003A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436863 | ||||||
chr11:27437297 | AT | A | 14 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147others(11): Show | 14 | HG00639.hp1 HG01099.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-24438delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437297 | ||||||
chr11:27437435 | C | T | 1 | a0001c0001t0007g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.186-24575G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437435 | ||||||
chr11:27437564 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.186-24704G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437564 | ||||||
chr11:27437660 | A | AGGTGTGT others(4): Show |
1 | a0001c0001t0012g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.186-24801_186-2480 others(15): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGT | 15 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0208others(12): Show | 15 | HG01099.hp1 HG01255.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-24802_186-2480 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGTGT | 17 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(14): Show | 17 | HG00639.hp1 HG02027.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.186-24804_186-2480 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGTGTGT | 47 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(44): Show | 47 | HG00735.hp2 HG01255.hp2 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.186-24806_186-2480 others(10): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGTGTGTG others(1): Show |
33 | a0001c0001t0001g0090a0001c0001t0001g0114a0001c0001t0001g0115others(30): Show | 33 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-24808_186-2480 others(12): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGTGTGTG others(3): Show |
40 | a0001c0001t0001g0143a0001c0001t0002g0215a0001c0001t0003g0089others(37): Show | 41 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.186-24810_186-2480 others(14): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGTGTGTG others(5): Show |
8 | a0001c0001t0010g0058a0001c0001t0012g0085a0001c0001t0030g0167others(5): Show | 8 | HG02132.hp1 HG02970.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-24812_186-2480 others(16): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0003g0097a0001c0001t0032g0175a0002c0003t0004g0145 | 3 | HG01070.hp2 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.186-24814_186-2480 others(18): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | AGT | A | 11 | a0001c0001t0006g0234a0001c0001t0009g0183a0001c0001t0009g0221others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-24802_186-2480 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | AGTGT | A | 4 | a0001c0001t0007g0040a0001c0002t0004g0074a0001c0005t0014g0149others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-24804_186-2480 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437660 | AGTGTGTG others(7): Show |
A | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-24814_186-2480 others(18): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | ||||||
chr11:27437712 | A | T | 1 | a0001c0004t0013g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186-24852T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437712 | ||||||
chr11:27437771 | GCAGGAGG others(5): Show |
G | 83 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(80): Show | 83 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.186-24923_186-2491 others(16): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437771 | ||||||
chr11:27437805 | C | T | 16 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0160others(13): Show | 16 | HG01981.hp1 HG02004.hp2 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.186-24945G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437805 | ||||||
chr11:27438443 | T | C | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-25583A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438443 | ||||||
chr11:27438559 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186-25699C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438559 | ||||||
chr11:27438604 | A | G | 2 | a0001c0002t0017g0005a0001c0002t0017g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-25744T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438604 | ||||||
chr11:27438610 | A | C | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-25750T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438610 | ||||||
chr11:27438655 | GCCT | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-25798_186-2579 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438655 | ||||||
chr11:27438665 | A | G | 3 | a0002c0003t0006g0184a0002c0003t0006g0185a0002c0003t0006g0198 | 3 | HG02055.hp1 HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.186-25805T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438665 | ||||||
chr11:27438988 | C | T | 1 | a0001c0001t0024g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.186-26128G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438988 | ||||||
chr11:27439079 | A | G | 1 | a0005c0007t0001g0116 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.186-26219T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439079 | ||||||
chr11:27439092 | C | T | 2 | a0001c0001t0002g0229a0001c0002t0008g0191 | 2 | NA18612.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.186-26232G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439092 | ||||||
chr11:27439164 | T | C | 187 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.186-26304A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439164 | ||||||
chr11:27439169 | C | A | 1 | a0006c0008t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186-26309G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439169 | ||||||
chr11:27439207 | T | G | 1 | a0001c0002t0004g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.186-26347A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439207 | ||||||
chr11:27439221 | T | C | 69 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0003g0089others(66): Show | 70 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.186-26361A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439221 | ||||||
chr11:27439226 | C | G | 1 | a0001c0001t0010g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.186-26366G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439226 | ||||||
chr11:27439492 | C | A | 1 | a0005c0007t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-26632G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439492 | ||||||
chr11:27439609 | G | T | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.186-26749C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439609 | ||||||
chr11:27439684 | T | C | 2 | a0001c0005t0014g0149a0001c0005t0014g0154 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.186-26824A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439684 | ||||||
chr11:27439899 | CTCTT | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.186-27043_186-2704 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439899 | ||||||
chr11:27439901 | C | CT | 8 | a0001c0001t0002g0188a0001c0001t0002g0206a0001c0001t0002g0220others(5): Show | 8 | HG01891.hp1 HG01975.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-27042dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | ||||||
chr11:27439901 | CT | C | 14 | a0001c0001t0002g0218a0001c0001t0003g0069a0001c0001t0003g0078others(11): Show | 14 | HG01070.hp2 HG01256.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-27042delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | ||||||
chr11:27439901 | CTT | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(10): Show | 13 | HG00642.hp2 HG01243.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.186-27043_186-2704 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | ||||||
chr11:27439901 | CTTT | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-27044_186-2704 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | ||||||
chr11:27439928 | C | T | 2 | a0001c0001t0009g0183a0001c0001t0009g0221 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.186-27068G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439928 | ||||||
chr11:27439982 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.186-27122A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439982 | ||||||
chr11:27440023 | A | T | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-27163T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440023 | ||||||
chr11:27440066 | C | A | 1 | a0001c0002t0006g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-27206G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440066 | ||||||
chr11:27440232 | T | C | 73 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(70): Show | 73 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.186-27372A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440232 | ||||||
chr11:27440266 | G | A | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186-27406C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440266 | ||||||
chr11:27440645 | TTG | T | 22 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-27787_186-2778 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440645 | ||||||
chr11:27440683 | C | G | 165 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(162): Show | 166 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.186-27823G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440683 | ||||||
chr11:27440926 | A | G | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(6): Show | 9 | HG02572.hp1 HG02647.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-28066T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440926 | ||||||
chr11:27441190 | C | G | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-28330G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441190 | ||||||
chr11:27441258 | T | C | 81 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0152others(78): Show | 82 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.186-28398A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441258 | ||||||
chr11:27441324 | C | CAGCCTCT others(46): Show |
1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-28517_186-2846 others(57): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441324 | ||||||
chr11:27441399 | T | C | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.186-28539A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441399 | ||||||
chr11:27441626 | C | T | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.186-28766G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441626 | ||||||
chr11:27441648 | AAG | A | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-28790_186-2878 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441648 | ||||||
chr11:27441836 | G | A | 8 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0010others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-28976C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441836 | ||||||
chr11:27441900 | G | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0127others(3): Show | 6 | HG00733.hp1 HG01981.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-29040C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441900 | ||||||
chr11:27441931 | T | G | 1 | a0006c0008t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186-29071A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441931 | ||||||
chr11:27442017 | A | G | 83 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(80): Show | 83 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.186-29157T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442017 | ||||||
chr11:27442045 | A | G | 4 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0002t0004g0070others(1): Show | 4 | HG01256.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-29185T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442045 | ||||||
chr11:27442180 | G | C | 1 | a0006c0008t0009g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-29320C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442180 | ||||||
chr11:27442285 | A | G | 70 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(67): Show | 70 | HG00735.hp2 HG01070.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.186-29425T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442285 | ||||||
chr11:27442588 | C | T | 2 | a0001c0001t0002g0229a0001c0002t0008g0191 | 2 | NA18612.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.185+29530G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442588 | ||||||
chr11:27442714 | C | T | 6 | a0001c0001t0001g0143a0001c0001t0030g0167a0001c0002t0017g0005others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+29404G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442714 | ||||||
chr11:27442781 | A | C | 187 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.185+29337T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442781 | ||||||
chr11:27443082 | C | T | 27 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(24): Show | 27 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(24): Show |
intron_variant | MODIFIER | c.185+29036G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443082 | ||||||
chr11:27443186 | CA | C | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+28931delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443186 | ||||||
chr11:27443325 | C | T | 6 | a0001c0002t0004g0135a0001c0002t0005g0001a0001c0002t0005g0025others(3): Show | 7 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+28793G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443325 | ||||||
chr11:27443358 | G | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+28760C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443358 | ||||||
chr11:27443367 | C | G | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+28751G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443367 | ||||||
chr11:27443518 | A | G | 3 | a0001c0001t0001g0147a0001c0001t0003g0142a0003c0006t0002g0168 | 3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+28600T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443518 | ||||||
chr11:27443589 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.185+28529C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443589 | ||||||
chr11:27444044 | T | C | 64 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(61): Show | 64 | HG00735.hp2 HG01070.hp2 HG01255.hp2 others(61): Show |
intron_variant | MODIFIER | c.185+28074A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444044 | ||||||
chr11:27444094 | G | GA | 83 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(80): Show | 83 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.185+28023dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444094 | ||||||
chr11:27444478 | G | T | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185+27640C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444478 | ||||||
chr11:27444826 | G | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+27292C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444826 | ||||||
chr11:27444853 | C | A | 3 | a0001c0001t0009g0174a0001c0001t0009g0183a0001c0001t0009g0221 | 3 | HG02145.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.185+27265G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444853 | ||||||
chr11:27444891 | A | G | 21 | a0001c0001t0007g0014a0001c0001t0007g0019a0001c0001t0007g0039others(18): Show | 21 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+27227T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444891 | ||||||
chr11:27445007 | A | T | 2 | a0002c0003t0005g0045a0002c0003t0006g0207 | 2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.185+27111T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445007 | ||||||
chr11:27445040 | AGGCAGAA others(4): Show |
A | 3 | a0001c0001t0001g0147a0001c0001t0003g0142a0003c0006t0002g0168 | 3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+27067_185+2707 others(15): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445040 | ||||||
chr11:27445210 | G | A | 1 | a0001c0001t0007g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185+26908C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445210 | ||||||
chr11:27445233 | C | T | 3 | a0001c0001t0001g0147a0001c0001t0003g0142a0003c0006t0002g0168 | 3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+26885G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445233 | ||||||
chr11:27445256 | G | A | 1 | a0001c0001t0010g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.185+26862C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445256 | ||||||
chr11:27445272 | C | A | 2 | a0001c0002t0017g0005a0001c0002t0017g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185+26846G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445272 | ||||||
chr11:27445283 | G | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+26835C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445283 | ||||||
chr11:27445374 | G | A | 10 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0160others(7): Show | 10 | NA18951.hp1 NA18952.hp2 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+26744C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445374 | ||||||
chr11:27445453 | G | A | 1 | a0001c0002t0011g0144 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.185+26665C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445453 | ||||||
chr11:27445562 | A | C | 165 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(162): Show | 166 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.185+26556T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445562 | ||||||
chr11:27445564 | C | A | 8 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0010others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+26554G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445564 | ||||||
chr11:27445706 | G | A | 1 | a0001c0005t0014g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.185+26412C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445706 | ||||||
chr11:27445814 | T | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+26304A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445814 | ||||||
chr11:27445883 | T | TA | 72 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(69): Show | 72 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.185+26234dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445883 | ||||||
chr11:27446154 | T | A | 71 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(68): Show | 71 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.185+25964A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446154 | ||||||
chr11:27446170 | AT | A | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+25947delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446170 | ||||||
chr11:27446371 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.185+25747C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446371 | ||||||
chr11:27446436 | T | G | 1 | a0001c0001t0010g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.185+25682A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446436 | ||||||
chr11:27446681 | C | T | 1 | a0002c0003t0005g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.185+25437G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446681 | ||||||
chr11:27446736 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.185+25382C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446736 | ||||||
chr11:27446886 | G | A | 5 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0062others(2): Show | 5 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+25232C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446886 | ||||||
chr11:27446917 | G | C | 71 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(68): Show | 71 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.185+25201C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446917 | ||||||
chr11:27447048 | G | C | 22 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+25070C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447048 | ||||||
chr11:27447053 | G | A | 67 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0003g0089others(64): Show | 68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.185+25065C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447053 | ||||||
chr11:27447081 | T | C | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+25037A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447081 | ||||||
chr11:27447098 | C | T | 6 | a0001c0001t0001g0143a0001c0001t0030g0167a0001c0002t0017g0005others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+25020G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447098 | ||||||
chr11:27447196 | A | T | 11 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0234others(8): Show | 11 | HG01169.hp1 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.185+24922T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447196 | ||||||
chr11:27447389 | T | C | 1 | a0001c0001t0003g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.185+24729A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447389 | ||||||
chr11:27447426 | T | G | 22 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+24692A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447426 | ||||||
chr11:27447602 | T | A | 3 | a0001c0001t0001g0147a0001c0001t0003g0142a0003c0006t0002g0168 | 3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+24516A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447602 | ||||||
chr11:27447631 | A | G | 1 | a0001c0002t0011g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.185+24487T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447631 | ||||||
chr11:27448295 | C | CT | 71 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(68): Show | 71 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.185+23822dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448295 | ||||||
chr11:27448355 | T | C | 1 | a0001c0002t0005g0049 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.185+23763A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448355 | ||||||
chr11:27448417 | T | C | 93 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(90): Show | 94 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.185+23701A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448417 | ||||||
chr11:27448519 | C | G | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+23599G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448519 | ||||||
chr11:27448570 | G | A | 1 | a0005c0007t0001g0116 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.185+23548C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448570 | ||||||
chr11:27448571 | C | T | 1 | a0001c0004t0013g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.185+23547G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448571 | ||||||
chr11:27448683 | T | G | 1 | a0006c0008t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+23435A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448683 | ||||||
chr11:27448878 | A | G | 45 | a0001c0001t0001g0090a0001c0001t0003g0089a0001c0001t0003g0132others(42): Show | 46 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.185+23240T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448878 | ||||||
chr11:27448970 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.185+23148G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448970 | ||||||
chr11:27449195 | G | A | 1 | a0001c0001t0003g0162 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.185+22923C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449195 | ||||||
chr11:27449273 | AAT | A | 22 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+22843_185+2284 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449273 | ||||||
chr11:27449301 | A | G | 65 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0090others(62): Show | 66 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.185+22817T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449301 | ||||||
chr11:27449356 | G | A | 3 | a0001c0001t0001g0147a0001c0001t0003g0142a0003c0006t0002g0168 | 3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+22762C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449356 | ||||||
chr11:27449373 | C | A | 164 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(161): Show | 165 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.185+22745G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449373 | ||||||
chr11:27449404 | G | A | 4 | a0001c0002t0001g0139a0001c0002t0001g0148a0001c0002t0004g0141others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+22714C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449404 | ||||||
chr11:27449412 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.185+22706C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449412 | ||||||
chr11:27449808 | A | T | 2 | a0001c0001t0001g0147a0001c0001t0003g0142 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+22310T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449808 | ||||||
chr11:27449883 | A | C | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0027g0138others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+22235T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449883 | ||||||
chr11:27450049 | A | G | 46 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0003g0089others(43): Show | 47 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.185+22069T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450049 | ||||||
chr11:27450173 | A | C | 25 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.185+21945T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450173 | ||||||
chr11:27450275 | T | C | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0027g0138others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+21843A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450275 | ||||||
chr11:27450345 | T | A | 1 | a0001c0002t0004g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185+21773A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450345 | ||||||
chr11:27450545 | T | C | 1 | a0001c0002t0011g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.185+21573A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450545 | ||||||
chr11:27450582 | A | C | 21 | a0001c0001t0007g0014a0001c0001t0007g0019a0001c0001t0007g0039others(18): Show | 21 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+21536T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450582 | ||||||
chr11:27450582 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.185+21536T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450582 | ||||||
chr11:27450686 | G | C | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+21432C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450686 | ||||||
chr11:27450749 | T | C | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+21369A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450749 | ||||||
chr11:27451083 | C | T | 1 | a0006c0008t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+21035G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451083 | ||||||
chr11:27451115 | A | C | 1 | a0001c0001t0003g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+21003T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451115 | ||||||
chr11:27451158 | A | G | 6 | a0001c0002t0004g0135a0001c0002t0005g0001a0001c0002t0005g0025others(3): Show | 7 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+20960T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451158 | ||||||
chr11:27451230 | T | C | 71 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0098others(68): Show | 71 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.185+20888A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451230 | ||||||
chr11:27451233 | A | T | 1 | a0001c0002t0004g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.185+20885T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451233 | ||||||
chr11:27451425 | G | A | 6 | a0001c0001t0006g0234a0001c0002t0001g0139a0001c0002t0001g0148others(3): Show | 6 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+20693C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451425 | ||||||
chr11:27451521 | G | A | 27 | a0001c0001t0001g0143a0001c0001t0007g0014a0001c0001t0007g0019others(24): Show | 27 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(24): Show |
intron_variant | MODIFIER | c.185+20597C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451521 | ||||||
chr11:27451550 | T | C | 3 | a0001c0001t0036g0241a0001c0002t0018g0239a0001c0002t0018g0240 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.185+20568A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451550 | ||||||
chr11:27451911 | A | G | 2 | a0001c0002t0004g0070a0001c0002t0004g0071 | 2 | HG01256.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.185+20207T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451911 | ||||||
chr11:27452042 | A | T | 1 | a0001c0002t0008g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.185+20076T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452042 | ||||||
chr11:27452342 | C | T | 1 | a0002c0003t0006g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.185+19776G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452342 | ||||||
chr11:27452422 | C | A | 4 | a0002c0003t0006g0184a0002c0003t0006g0185a0002c0003t0006g0198others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+19696G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452422 | ||||||
chr11:27452434 | G | A | 86 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(83): Show | 86 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.185+19684C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452434 | ||||||
chr11:27452581 | AT | A | 83 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(80): Show | 83 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.185+19536delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452581 | ||||||
chr11:27452623 | G | GT | 32 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0114others(29): Show | 32 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.185+19494dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452623 | ||||||
chr11:27452623 | GT | G | 6 | a0001c0001t0002g0215a0001c0001t0007g0031a0001c0001t0007g0041others(3): Show | 6 | HG00639.hp1 HG01975.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+19494delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452623 | ||||||
chr11:27452623 | GTTT | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+19492_185+1949 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452623 | ||||||
chr11:27452650 | CA | C | 56 | a0001c0001t0003g0132a0001c0001t0007g0014a0001c0001t0007g0016others(53): Show | 57 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.185+19467delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452650 | ||||||
chr11:27452759 | G | T | 10 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0152others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+19359C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452759 | ||||||
chr11:27452784 | C | T | 1 | a0001c0002t0004g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.185+19334G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452784 | ||||||
chr11:27452790 | A | AT | 5 | a0001c0001t0002g0220a0001c0001t0010g0015a0001c0002t0004g0073others(2): Show | 5 | HG00544.hp1 HG02135.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+19327dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452790 | ||||||
chr11:27452823 | C | T | 5 | a0001c0001t0001g0143a0001c0002t0001g0139a0001c0002t0001g0148others(2): Show | 5 | HG00642.hp2 HG01243.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+19295G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452823 | ||||||
chr11:27453248 | T | C | 56 | a0001c0001t0003g0132a0001c0001t0007g0014a0001c0001t0007g0016others(53): Show | 57 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.185+18870A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453248 | ||||||
chr11:27453345 | G | A | 1 | a0001c0001t0010g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.185+18773C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453345 | ||||||
chr11:27453358 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.185+18760G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453358 | ||||||
chr11:27453362 | C | G | 1 | a0001c0001t0032g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185+18756G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453362 | ||||||
chr11:27453443 | T | TA | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0152others(6): Show | 9 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+18674dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453443 | ||||||
chr11:27454161 | C | T | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0152others(6): Show | 9 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+17957G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454161 | ||||||
chr11:27454514 | C | G | 1 | a0007c0013t0004g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.185+17604G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454514 | ||||||
chr11:27454552 | G | A | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0152others(6): Show | 9 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+17566C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454552 | ||||||
chr11:27454761 | C | CA | 16 | a0001c0001t0001g0111a0001c0001t0002g0173a0001c0001t0010g0058others(13): Show | 16 | HG01433.hp1 HG01981.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+17356dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454761 | ||||||
chr11:27454761 | CA | C | 61 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(58): Show | 61 | HG00408.hp1 HG00544.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.185+17356delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454761 | ||||||
chr11:27454963 | A | C | 1 | a0001c0001t0003g0130 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+17155T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454963 | ||||||
chr11:27455079 | A | C | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+17039T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455079 | ||||||
chr11:27455252 | C | T | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+16866G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455252 | ||||||
chr11:27455269 | G | A | 11 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0210others(8): Show | 11 | HG00609.hp2 HG01975.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+16849C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455269 | ||||||
chr11:27455350 | T | G | 1 | a0001c0002t0004g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.185+16768A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455350 | ||||||
chr11:27455389 | A | C | 66 | a0001c0001t0001g0143a0001c0001t0003g0132a0001c0001t0003g0142others(63): Show | 67 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.185+16729T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455389 | ||||||
chr11:27455727 | C | T | 2 | a0001c0001t0003g0134a0001c0002t0004g0133 | 2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.185+16391G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455727 | ||||||
chr11:27455756 | T | C | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+16362A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455756 | ||||||
chr11:27455769 | C | T | 2 | a0001c0002t0005g0023a0001c0002t0005g0024 | 2 | NA18946.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.185+16349G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455769 | ||||||
chr11:27455887 | G | C | 1 | a0001c0002t0006g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.185+16231C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455887 | ||||||
chr11:27456303 | C | T | 1 | a0002c0003t0006g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185+15815G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27456303 | ||||||
chr11:27456317 | A | AAC | 146 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(143): Show | 147 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.185+15799_185+1580 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27456317 | ||||||
chr11:27456326 | T | C | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+15792A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27456326 | ||||||
chr11:27457030 | T | C | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+15088A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457030 | ||||||
chr11:27457044 | AG | A | 8 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0010others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+15073delC | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457044 | ||||||
chr11:27457223 | G | T | 1 | a0001c0002t0005g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.185+14895C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457223 | ||||||
chr11:27457409 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.185+14709C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457409 | ||||||
chr11:27457491 | C | A | 2 | a0001c0004t0013g0013a0001c0004t0013g0046 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.185+14627G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457491 | ||||||
chr11:27457534 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185+14584G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457534 | ||||||
chr11:27458100 | G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147 | 3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+14018C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458100 | ||||||
chr11:27458365 | T | C | 2 | a0001c0002t0008g0196a0001c0002t0033g0171 | 2 | NA18960.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.185+13753A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458365 | ||||||
chr11:27458378 | A | G | 1 | a0002c0003t0006g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.185+13740T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458378 | ||||||
chr11:27458457 | T | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+13661A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458457 | ||||||
chr11:27458518 | T | G | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+13600A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458518 | ||||||
chr11:27458586 | T | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+13532A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458586 | ||||||
chr11:27458601 | C | T | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+13517G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458601 | ||||||
chr11:27458669 | G | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+13449C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458669 | ||||||
chr11:27459076 | T | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+13042A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459076 | ||||||
chr11:27459147 | G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147 | 3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+12971C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459147 | ||||||
chr11:27459280 | T | C | 66 | a0001c0001t0001g0143a0001c0001t0003g0132a0001c0001t0003g0142others(63): Show | 67 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.185+12838A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459280 | ||||||
chr11:27459315 | G | C | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0019g0003others(5): Show | 8 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+12803C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459315 | ||||||
chr11:27459522 | G | T | 1 | a0001c0001t0010g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.185+12596C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459522 | ||||||
chr11:27459711 | A | G | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+12407T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459711 | ||||||
chr11:27459874 | T | C | 1 | a0001c0001t0003g0159 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.185+12244A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459874 | ||||||
chr11:27460052 | T | C | 2 | a0001c0002t0017g0005a0001c0002t0017g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185+12066A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460052 | ||||||
chr11:27460211 | G | C | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.185+11907C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460211 | ||||||
chr11:27460356 | TAA | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+11760_185+1176 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460356 | ||||||
chr11:27460454 | C | T | 8 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0010others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+11664G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460454 | ||||||
chr11:27460805 | T | C | 165 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.185+11313A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460805 | ||||||
chr11:27461048 | C | T | 2 | a0001c0001t0009g0177a0001c0002t0006g0197 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.185+11070G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461048 | ||||||
chr11:27461084 | T | C | 1 | a0001c0004t0035g0176 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.185+11034A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461084 | ||||||
chr11:27461354 | A | T | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+10764T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461354 | ||||||
chr11:27461366 | A | T | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185+10752T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461366 | ||||||
chr11:27461632 | A | AT | 55 | a0001c0001t0003g0132a0001c0001t0007g0014a0001c0001t0007g0016others(52): Show | 56 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.185+10485dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461632 | ||||||
chr11:27461715 | T | C | 165 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.185+10403A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461715 | ||||||
chr11:27461836 | A | AT | 96 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.185+10281dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | ||||||
chr11:27461836 | A | ATT | 54 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0078others(51): Show | 55 | HG00099.hp2 HG00544.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.185+10280_185+1028 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | ||||||
chr11:27461836 | A | ATTT | 15 | a0001c0001t0007g0016a0001c0001t0007g0019a0001c0001t0007g0020others(12): Show | 15 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.185+10279_185+1028 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | ||||||
chr11:27461836 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185+10271_185+1028 others(15): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | ||||||
chr11:27461870 | G | C | 1 | a0001c0001t0002g0218 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.185+10248C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461870 | ||||||
chr11:27461923 | G | A | 21 | a0001c0001t0007g0014a0001c0001t0007g0039a0001c0001t0007g0040others(18): Show | 21 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+10195C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461923 | ||||||
chr11:27462084 | C | T | 1 | a0001c0002t0008g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.185+10034G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462084 | ||||||
chr11:27462085 | G | A | 1 | a0001c0002t0006g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185+10033C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462085 | ||||||
chr11:27462231 | G | A | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+9887C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462231 | ||||||
chr11:27462287 | G | A | 23 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0202others(20): Show | 23 | HG00408.hp2 HG01943.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.185+9831C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462287 | ||||||
chr11:27463067 | C | CA | 88 | a0001c0001t0001g0060a0001c0001t0001g0083a0001c0001t0001g0090others(85): Show | 88 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.185+9050dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | ||||||
chr11:27463067 | C | CAA | 46 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0131others(43): Show | 46 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.185+9049_185+9050d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | ||||||
chr11:27463067 | C | CAAA | 8 | a0001c0001t0001g0128a0001c0001t0001g0143a0001c0001t0002g0218others(5): Show | 8 | HG00140.hp1 HG02071.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+9048_185+9050d others(5): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | ||||||
chr11:27463067 | CA | C | 46 | a0001c0001t0007g0014a0001c0001t0007g0016a0001c0001t0007g0019others(43): Show | 47 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.185+9050delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | ||||||
chr11:27463067 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0157 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.185+9040_185+9050d others(13): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | ||||||
chr11:27463135 | C | G | 1 | a0001c0002t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.185+8983G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463135 | ||||||
chr11:27463160 | G | A | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+8958C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463160 | ||||||
chr11:27463188 | G | A | 66 | a0001c0001t0001g0143a0001c0001t0003g0132a0001c0001t0003g0142others(63): Show | 67 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.185+8930C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463188 | ||||||
chr11:27463307 | A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147 | 3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+8811T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463307 | ||||||
chr11:27463470 | A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+8648T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463470 | ||||||
chr11:27463809 | A | C | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+8309T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463809 | ||||||
chr11:27463824 | T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+8294A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463824 | ||||||
chr11:27464205 | G | C | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+7913C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464205 | ||||||
chr11:27464425 | C | T | 1 | a0001c0001t0009g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.185+7693G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464425 | ||||||
chr11:27464468 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.185+7650C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464468 | ||||||
chr11:27464589 | C | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.185+7529G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464589 | ||||||
chr11:27464807 | T | C | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185+7311A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464807 | ||||||
chr11:27464839 | G | A | 1 | a0001c0002t0006g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+7279C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464839 | ||||||
chr11:27465268 | A | G | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+6850T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465268 | ||||||
chr11:27465274 | T | C | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+6844A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465274 | ||||||
chr11:27465395 | C | T | 4 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0002t0004g0070others(1): Show | 4 | HG01256.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+6723G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465395 | ||||||
chr11:27465670 | G | A | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+6448C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465670 | ||||||
chr11:27465914 | C | T | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+6204G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465914 | ||||||
chr11:27466220 | A | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+5898T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466220 | ||||||
chr11:27466445 | C | T | 86 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.185+5673G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466445 | ||||||
chr11:27466564 | T | G | 1 | a0002c0003t0004g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185+5554A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466564 | ||||||
chr11:27466695 | G | A | 1 | a0003c0006t0002g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185+5423C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466695 | ||||||
chr11:27466940 | C | T | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.185+5178G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466940 | ||||||
chr11:27467034 | C | T | 1 | a0001c0001t0027g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+5084G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467034 | ||||||
chr11:27467064 | G | A | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+5054C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467064 | ||||||
chr11:27467291 | G | C | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+4827C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467291 | ||||||
chr11:27467296 | G | A | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+4822C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467296 | ||||||
chr11:27467334 | G | A | 1 | a0001c0002t0006g0219 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.185+4784C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467334 | ||||||
chr11:27467456 | C | T | 164 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0083others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.185+4662G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467456 | ||||||
chr11:27467480 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.185+4638A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467480 | ||||||
chr11:27467551 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.185+4567G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467551 | ||||||
chr11:27467566 | C | CA | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0002g0227others(6): Show | 9 | HG02055.hp2 HG02132.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.185+4551dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467566 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0004g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.185+4551_185+4552i others(21): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467566 | C | CAAAAAAA others(14): Show |
1 | a0001c0005t0014g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.185+4551_185+4552i others(23): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467566 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.185+4551_185+4552i others(25): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467566 | C | CAAAAAAA others(17): Show |
2 | a0001c0005t0014g0149a0001c0005t0014g0154 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.185+4551_185+4552i others(26): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467566 | C | CAAAAAAA others(18): Show |
1 | a0001c0005t0014g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185+4551_185+4552i others(27): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467566 | CA | C | 5 | a0001c0001t0007g0014a0001c0001t0019g0003a0001c0002t0008g0170others(2): Show | 5 | HG02622.hp2 HG02895.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+4551delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | ||||||
chr11:27467581 | A | AC | 85 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.185+4536_185+4537i others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467581 | ||||||
chr11:27467789 | G | C | 2 | a0001c0002t0017g0005a0001c0002t0017g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185+4329C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467789 | ||||||
chr11:27467851 | G | A | 1 | a0006c0008t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+4267C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467851 | ||||||
chr11:27468095 | T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0147 | 3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+4023A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468095 | ||||||
chr11:27468112 | GA | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+4005delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468112 | ||||||
chr11:27468155 | A | G | 1 | a0001c0002t0004g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.185+3963T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468155 | ||||||
chr11:27468253 | G | C | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0230 | 3 | NA18974.hp1 NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.185+3865C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468253 | ||||||
chr11:27468311 | T | A | 7 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(4): Show | 7 | NA18971.hp1 NA18974.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+3807A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468311 | ||||||
chr11:27468401 | C | T | 1 | a0001c0002t0004g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.185+3717G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468401 | ||||||
chr11:27468422 | G | A | 1 | a0001c0005t0014g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.185+3696C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468422 | ||||||
chr11:27468528 | T | C | 1 | a0001c0002t0005g0049 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.185+3590A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468528 | ||||||
chr11:27468585 | A | G | 3 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0002t0004g0061 | 3 | HG01515.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.185+3533T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468585 | ||||||
chr11:27468701 | GA | G | 85 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.185+3416delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468701 | ||||||
chr11:27468715 | A | G | 3 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0002t0004g0061 | 3 | HG01515.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.185+3403T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468715 | ||||||
chr11:27469040 | G | A | 6 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0010others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+3078C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469040 | ||||||
chr11:27469115 | A | T | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+3003T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469115 | ||||||
chr11:27469242 | C | T | 3 | a0001c0001t0036g0241a0001c0002t0018g0239a0001c0002t0018g0240 | 3 | HG02486.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.185+2876G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469242 | ||||||
chr11:27469319 | T | G | 3 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166 | 3 | NA19006.hp2 NA19070.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.185+2799A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469319 | ||||||
chr11:27469432 | C | T | 1 | a0007c0013t0004g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.185+2686G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469432 | ||||||
chr11:27469529 | T | A | 1 | a0001c0002t0008g0228 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.185+2589A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469529 | ||||||
chr11:27469559 | C | A | 1 | a0001c0001t0019g0003 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+2559G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469559 | ||||||
chr11:27469769 | G | A | 1 | a0001c0001t0036g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.185+2349C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469769 | ||||||
chr11:27470074 | A | G | 1 | a0001c0004t0013g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.185+2044T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470074 | ||||||
chr11:27470713 | G | GA | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0002g0229others(5): Show | 8 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1404dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470713 | ||||||
chr11:27470713 | GA | G | 88 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.185+1404delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470713 | ||||||
chr11:27470867 | G | C | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | NA18946.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.185+1251C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470867 | ||||||
chr11:27471058 | T | G | 1 | a0002c0012t0003g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+1060A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471058 | ||||||
chr11:27471112 | A | T | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+1006T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471112 | ||||||
chr11:27471418 | T | G | 1 | a0001c0001t0003g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.185+700A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471418 | ||||||
chr11:27471554 | C | G | 1 | a0001c0001t0006g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+564G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471554 | ||||||
chr11:27471787 | C | G | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+331G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471787 | ||||||
chr11:27471856 | G | A | 1 | a0001c0002t0006g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+262C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471856 | ||||||
chr11:27471981 | A | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0004g0151others(4): Show | 7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+137T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471981 | ||||||
chr11:27472020 | C | A | 3 | a0001c0001t0003g0134a0001c0002t0004g0133a0001c0002t0004g0135 | 3 | HG00099.hp2 HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.185+98G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472020 | ||||||
chr11:27472074 | C | A | 2 | a0001c0001t0001g0137a0001c0002t0004g0136 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.185+44G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472074 | ||||||
chr11:27472083 | T | TC | 22 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0002g0235others(19): Show | 22 | HG00544.hp2 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.185+34dupG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472083 | ||||||
chr11:27472083 | TC | T | 93 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0095others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.185+34delG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472083 | ||||||
chr11:27472090 | C | A | 10 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0160others(7): Show | 10 | NA18951.hp1 NA18952.hp2 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+28G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472090 | ||||||
chr11:27472090 | C | G | 1 | a0001c0002t0004g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185+28G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472090 | ||||||
chr11:27472091 | C | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+27G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472091 |