Item | Value |
---|---|
geneid | 3936 |
ensemblid | ENSG00000136167.15 |
hgncid | 6528 |
symbol | LCP1 |
name | lymphocyte cytosolic protein 1 |
refseq_nuc | NM_002298.5 |
refseq_prot | NP_002289.2 |
ensembl_nuc | ENST00000323076.7 |
ensembl_prot | ENSP00000315757.2 |
mane_status | MANE Select |
chr | chr13 |
start | 46125923 |
end | 46182177 |
strand | - |
ver | v1.2 |
region | chr13:46125923-46182177 |
region5000 | chr13:46120923-46187177 |
regionname0 | LCP1_chr13_46125923_46182177 |
regionname5000 | LCP1_chr13_46120923_46187177 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 627 | 333 | 62 | 66 | 151 | 13 | 40 | 115 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002 | 1/0 | 627 | 44 | 20 | 12 | 10 | 1 | 0 | 6 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0003 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0004 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0005 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0006 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0007 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1884 | 310 | 61 | 59 | 142 | 12 | 35 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0002 | 1/0 | 1884 | 44 | 20 | 12 | 10 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0003 | 0/0 | 1884 | 16 | 1 | 6 | 3 | 1 | 5 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0004 | 0/0 | 1884 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0005 | 0/0 | 1884 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0006 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0007 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0008 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0009 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0010 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0011 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0012 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
c0013 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1760 | 137 | 16 | 32 | 71 | 4 | 14 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0002 | 0/0 | 1760 | 120 | 18 | 21 | 57 | 7 | 17 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0003 | 0/0 | 1760 | 34 | 21 | 4 | 9 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0004 | 0/0 | 1760 | 20 | 2 | 7 | 5 | 1 | 5 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0005 | 1/0 | 1760 | 15 | 1 | 8 | 4 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0006 | 0/0 | 1760 | 13 | 7 | 0 | 6 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0007 | 0/0 | 1760 | 6 | 6 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0008 | 0/0 | 1760 | 4 | 0 | 0 | 4 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0009 | 0/0 | 1760 | 4 | 4 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0010 | 0/0 | 1760 | 4 | 0 | 4 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0011 | 0/0 | 1760 | 3 | 3 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0012 | 0/0 | 1760 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0013 | 0/0 | 1760 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0014 | 0/0 | 1760 | 2 | 0 | 0 | 1 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0015 | 0/0 | 1760 | 2 | 0 | 0 | 1 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0016 | 0/0 | 1760 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0017 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0018 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0019 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0020 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0021 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0022 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0023 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0024 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0025 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0026 | 0/0 | 1760 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0027 | 0/1 | 1760 | 1 | 0 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
t0028 | 0/0 | 1760 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0007 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0347 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1884 | 310 | 61 | 59 | 142 | 12 | 35 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0001c0003 | 0/0 | 1884 | 16 | 1 | 6 | 3 | 1 | 5 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0001c0004 | 0/0 | 1884 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0001c0005 | 0/0 | 1884 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0001c0008 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0001c0009 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0001c0010 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0002c0002 | 1/0 | 1884 | 44 | 20 | 12 | 10 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0003c0006 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0004c0007 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0005c0012 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0006c0011 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 | |
a0007c0013 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3643 | 130 | 14 | 32 | 66 | 4 | 14 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0002 | 0/0 | 3643 | 115 | 17 | 20 | 54 | 7 | 17 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0003 | 0/0 | 3643 | 10 | 6 | 0 | 4 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0004 | 0/0 | 3643 | 6 | 1 | 1 | 4 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0006 | 0/0 | 3643 | 10 | 7 | 0 | 3 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0007 | 0/0 | 3643 | 5 | 5 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0008 | 0/0 | 3643 | 4 | 0 | 0 | 4 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0009 | 0/0 | 3643 | 4 | 4 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0010 | 0/0 | 3643 | 4 | 0 | 4 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0011 | 0/0 | 3643 | 3 | 3 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0012 | 0/0 | 3643 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0013 | 0/0 | 3643 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0014 | 0/0 | 3643 | 2 | 0 | 0 | 1 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0015 | 0/0 | 3643 | 2 | 0 | 0 | 1 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0017 | 0/0 | 3643 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0018 | 0/0 | 3643 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0019 | 0/0 | 3643 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0020 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0022 | 0/0 | 3643 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0023 | 0/0 | 3643 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0024 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0025 | 0/0 | 3643 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0026 | 0/0 | 3643 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0027 | 0/1 | 3643 | 1 | 0 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0001t0028 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0003t0001 | 0/0 | 3643 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0003t0004 | 0/0 | 3643 | 14 | 1 | 6 | 1 | 1 | 5 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0004t0006 | 0/0 | 3643 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0005t0001 | 0/0 | 3643 | 2 | 0 | 0 | 2 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0008t0002 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0009t0002 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0001c0010t0002 | 0/0 | 3643 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002c0002t0001 | 0/0 | 3643 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002c0002t0003 | 0/0 | 3643 | 23 | 14 | 4 | 5 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002c0002t0005 | 1/0 | 3643 | 15 | 1 | 8 | 4 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002c0002t0006 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002c0002t0007 | 0/0 | 3643 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0002c0002t0016 | 0/0 | 3643 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0003c0006t0003 | 0/0 | 3643 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0004c0007t0002 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0005c0012t0002 | 0/0 | 3643 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0006c0011t0021 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
a0007c0013t0001 | 0/0 | 3643 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | copy fasta | chr13 | 46120923 | 46187177 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0008g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0010g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0010g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0010g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0010g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0011g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0012g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0014g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0015g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0015g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0017g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0018g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0019g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0020g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0022g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0023g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0024g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0025g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0026g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0027g0347 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0001t0028g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0003t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0004t0006g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0004t0006g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0008t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0009t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0001c0010t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0007 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0005g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0016g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0002c0002t0016g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0003c0006t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0004c0007t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0005c0012t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0006c0011t0021g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
a0007c0013t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0237 | EUR | GBR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0337 | EUR | GBR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00140 | hp2 | a0001 | c0001 | t0025 | g0173 | EUR | GBR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0281 | EUR | FIN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00323 | hp2 | a0001 | c0003 | t0004 | g0329 | EUR | FIN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0050 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0355 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00673 | hp1 | a0002 | c0002 | t0005 | g0028 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00673 | hp2 | a0001 | c0001 | t0024 | g0026 | EAS | CHS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00733 | hp1 | a0001 | c0003 | t0004 | g0354 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00738 | hp1 | a0002 | c0002 | t0005 | g0328 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01070 | hp1 | a0001 | c0001 | t0010 | g0338 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01070 | hp2 | a0002 | c0002 | t0003 | g0248 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01071 | hp2 | a0001 | c0001 | t0010 | g0339 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0179 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0280 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0172 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01109 | hp2 | a0001 | c0001 | t0022 | g0133 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01167 | hp2 | a0002 | c0002 | t0005 | g0342 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01168 | hp1 | a0001 | c0003 | t0004 | g0001 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01169 | hp1 | a0001 | c0003 | t0004 | g0001 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01169 | hp2 | a0002 | c0002 | t0005 | g0341 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01192 | hp1 | a0001 | c0001 | t0017 | g0292 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01255 | hp2 | a0002 | c0002 | t0005 | g0129 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01257 | hp1 | a0001 | c0003 | t0004 | g0224 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01257 | hp2 | a0002 | c0002 | t0005 | g0003 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01258 | hp2 | a0002 | c0002 | t0005 | g0003 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01346 | hp1 | a0001 | c0003 | t0004 | g0160 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0245 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | IBS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | IBS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01517 | hp2 | a0002 | c0002 | t0005 | g0007 | EUR | IBS | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0331 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0231 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01943 | hp2 | a0002 | c0002 | t0005 | g0360 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0198 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01981 | hp2 | a0001 | c0010 | t0002 | g0226 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02040 | hp1 | a0002 | c0002 | t0005 | g0370 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02055 | hp2 | a0001 | c0003 | t0004 | g0335 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02056 | hp1 | a0001 | c0001 | t0014 | g0275 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02080 | hp2 | a0001 | c0008 | t0002 | g0067 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02083 | hp2 | a0001 | c0001 | t0015 | g0324 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02129 | hp1 | a0007 | c0013 | t0001 | g0031 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02135 | hp1 | a0006 | c0011 | t0021 | g0069 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02135 | hp2 | a0002 | c0002 | t0005 | g0103 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02145 | hp1 | a0002 | c0002 | t0003 | g0187 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0095 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02148 | hp1 | a0001 | c0001 | t0010 | g0314 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CDX | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02165 | hp2 | a0002 | c0002 | t0005 | g0098 | EAS | CDX | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02257 | hp2 | a0001 | c0001 | t0013 | g0016 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0321 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0250 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0310 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0356 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0303 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02723 | hp2 | a0002 | c0002 | t0016 | g0311 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02735 | hp2 | a0001 | c0003 | t0004 | g0301 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02738 | hp1 | a0001 | c0003 | t0004 | g0302 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0209 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0336 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02818 | hp1 | a0002 | c0002 | t0003 | g0229 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02886 | hp2 | a0002 | c0002 | t0003 | g0238 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02895 | hp1 | a0001 | c0001 | t0011 | g0246 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0241 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02896 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0242 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0247 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0200 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02965 | hp1 | a0002 | c0002 | t0003 | g0249 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0039 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02976 | hp1 | a0002 | c0002 | t0016 | g0191 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0217 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0276 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03195 | hp2 | a0002 | c0002 | t0003 | g0190 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03209 | hp2 | a0001 | c0001 | t0026 | g0184 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0204 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0182 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03490 | hp1 | a0001 | c0003 | t0004 | g0002 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03490 | hp2 | a0001 | c0001 | t0014 | g0365 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03491 | hp2 | a0001 | c0001 | t0018 | g0152 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03492 | hp1 | a0001 | c0003 | t0004 | g0002 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | ESN | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03688 | hp1 | a0001 | c0001 | t0019 | g0055 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0326 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03927 | hp1 | a0001 | c0001 | t0015 | g0346 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG04228 | hp1 | a0001 | c0003 | t0004 | g0078 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0361 | SAS | STU | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18522 | hp2 | a0003 | c0006 | t0003 | g0203 | AFR | YRI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CHB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | YRI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | YRI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0089 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18942 | hp1 | a0001 | c0001 | t0012 | g0362 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18946 | hp2 | a0001 | c0005 | t0001 | g0169 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18953 | hp2 | a0002 | c0002 | t0006 | g0104 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18954 | hp1 | a0001 | c0001 | t0020 | g0112 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18962 | hp2 | a0001 | c0003 | t0004 | g0166 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18966 | hp2 | a0001 | c0001 | t0008 | g0372 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18980 | hp1 | a0001 | c0009 | t0002 | g0085 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18980 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18981 | hp1 | a0001 | c0001 | t0028 | g0374 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18983 | hp1 | a0001 | c0004 | t0006 | g0352 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18985 | hp1 | a0001 | c0001 | t0006 | g0305 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18986 | hp1 | a0001 | c0004 | t0006 | g0358 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18986 | hp2 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18995 | hp2 | a0002 | c0002 | t0003 | g0032 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18997 | hp1 | a0001 | c0005 | t0001 | g0154 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19001 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19003 | hp1 | a0004 | c0007 | t0002 | g0140 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0340 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19010 | hp1 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19030 | hp1 | a0002 | c0002 | t0005 | g0072 | AFR | LWK | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | LWK | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0371 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19062 | hp2 | a0001 | c0001 | t0012 | g0159 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0373 | EAS | JPT | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20129 | hp1 | a0002 | c0002 | t0007 | g0309 | AFR | ASW | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ASW | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0363 | EUR | TSI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0345 | EUR | TSI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0293 | EUR | TSI | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | GIH | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | GIH | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG01123 | hp2 | a0002 | c0002 | t0005 | g0366 | AMR | CLM | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | ACB | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0189 | AFR | MSL | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
HG06807 | hp2 | a0005 | c0012 | t0002 | g0195 | AFR | USA | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20300 | hp1 | a0001 | c0001 | t0023 | g0194 | AFR | USA | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0202 | AFR | USA | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | LWK | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0235 | AFR | LWK | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0027 | g0347 | REF | REF | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0005 | g0007 | REF | REF | LCP1_chr13_46120923_46187177 | LCP1 | chr13 | 46120923 | 46187177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46130923 | T | C | 1 | a0006 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1642A>G | p.Thr548Ala | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1733/3643 | 1642/1884 | 548/627 | chr13 | 46130923 | ||
chr13:46130935 | G | C | 1 | a0005 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1630C>G | p.Pro544Ala | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1721/3643 | 1630/1884 | 544/627 | chr13 | 46130935 | ||
chr13:46134156 | T | C | 6 | a0001a0003a0004others(3): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
missense_variant | MODERATE | c.1597A>G | p.Lys533Glu | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/16 | 1688/3643 | 1597/1884 | 533/627 | chr13 | 46134156 | ||
chr13:46151048 | C | T | 1 | a0004 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.770G>A | p.Ser257Asn | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/16 | 861/3643 | 770/1884 | 257/627 | chr13 | 46151048 | ||
chr13:46151070 | C | A | 1 | a0007 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.748G>T | p.Ala250Ser | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/16 | 839/3643 | 748/1884 | 250/627 | chr13 | 46151070 | ||
chr13:46156507 | C | T | 1 | a0003 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.422G>A | p.Arg141Gln | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/16 | 513/3643 | 422/1884 | 141/627 | chr13 | 46156507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46130816 | T | C | 1 | a0001c0004 | 2 | NA18983.hp1 NA18986.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1749A>G | p.Ala583Ala | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1840/3643 | 1749/1884 | 583/627 | chr13 | 46130816 | ||
chr13:46130840 | A | G | 1 | a0001c0009 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.1725T>C | p.Asn575Asn | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1816/3643 | 1725/1884 | 575/627 | chr13 | 46130840 | ||
chr13:46130897 | G | A | 1 | a0001c0010 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.1668C>T | p.Ile556Ile | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1759/3643 | 1668/1884 | 556/627 | chr13 | 46130897 | ||
chr13:46130933 | C | A | 3 | a0001c0003a0001c0005a0007c0013 | 19 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(16): Show |
synonymous_variant | LOW | c.1632G>T | p.Pro544Pro | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1723/3643 | 1632/1884 | 544/627 | chr13 | 46130933 | ||
chr13:46130933 | C | T | 1 | a0001c0008 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.1632G>A | p.Pro544Pro | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/16 | 1723/3643 | 1632/1884 | 544/627 | chr13 | 46130933 | ||
chr13:46142408 | G | A | 1 | a0001c0005 | 2 | NA18946.hp2 NA18997.hp1 |
synonymous_variant | LOW | c.1386C>T | p.Tyr462Tyr | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/16 | 1477/3643 | 1386/1884 | 462/627 | chr13 | 46142408 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46125927 | G | A | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0020others(6): Show | 143 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1664 | chr13 | 46125927 | |||||
chr13:46126038 | G | T | 1 | a0001c0001t0008 | 4 | HG00423.hp1 NA18966.hp2 NA18986.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1553C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1553 | chr13 | 46126038 | |||||
chr13:46126109 | G | C | 1 | a0001c0001t0014 | 2 | HG02056.hp1 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1482C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1482 | chr13 | 46126109 | |||||
chr13:46126186 | A | G | 1 | a0001c0001t0009 | 4 | HG02723.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1405T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1405 | chr13 | 46126186 | |||||
chr13:46126267 | A | G | 1 | a0001c0001t0009 | 4 | HG02723.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1324T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1324 | chr13 | 46126267 | |||||
chr13:46126443 | T | C | 2 | a0001c0001t0009a0001c0001t0022 | 5 | HG01109.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1148A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1148 | chr13 | 46126443 | |||||
chr13:46126464 | T | G | 1 | a0001c0001t0011 | 3 | HG02895.hp1 HG02897.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1127A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1127 | chr13 | 46126464 | |||||
chr13:46126478 | A | T | 3 | a0001c0001t0007a0001c0001t0023a0002c0002t0007 | 7 | HG01891.hp1 HG02809.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1113T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1113 | chr13 | 46126478 | |||||
chr13:46126507 | G | T | 15 | a0001c0001t0002a0001c0001t0008a0001c0001t0012others(12): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1084C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 1084 | chr13 | 46126507 | |||||
chr13:46126610 | C | A | 1 | a0001c0001t0024 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 981 | chr13 | 46126610 | |||||
chr13:46126650 | T | C | 2 | a0001c0001t0009a0001c0001t0022 | 5 | HG01109.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*941A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 941 | chr13 | 46126650 | |||||
chr13:46126685 | C | T | 1 | a0001c0001t0026 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*906G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 906 | chr13 | 46126685 | |||||
chr13:46126690 | T | C | 1 | a0001c0001t0025 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 901 | chr13 | 46126690 | |||||
chr13:46126895 | A | C | 1 | a0001c0001t0019 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*696T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 696 | chr13 | 46126895 | |||||
chr13:46126967 | A | C | 1 | a0001c0001t0018 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 624 | chr13 | 46126967 | |||||
chr13:46127038 | G | A | 1 | a0006c0011t0021 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 553 | chr13 | 46127038 | |||||
chr13:46127039 | G | C | 3 | a0001c0001t0004a0001c0001t0028a0001c0003t0004 | 21 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*552C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 552 | chr13 | 46127039 | |||||
chr13:46127056 | C | T | 2 | a0001c0001t0022a0002c0002t0016 | 3 | HG01109.hp2 HG02723.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*535G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 535 | chr13 | 46127056 | |||||
chr13:46127071 | G | A | 1 | a0001c0001t0015 | 2 | HG02083.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 520 | chr13 | 46127071 | |||||
chr13:46127098 | A | T | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
3_prime_UTR_variant | MODIFIER | c.*493T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 493 | chr13 | 46127098 | |||||
chr13:46127203 | C | T | 2 | a0001c0001t0007a0002c0002t0007 | 6 | HG01891.hp1 HG02809.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*388G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 388 | chr13 | 46127203 | |||||
chr13:46127236 | T | A | 20 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(17): Show | 173 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 355 | chr13 | 46127236 | |||||
chr13:46127445 | G | T | 1 | a0001c0001t0017 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 146 | chr13 | 46127445 | |||||
chr13:46127542 | C | T | 2 | a0001c0001t0012a0001c0001t0013 | 4 | HG02257.hp2 NA18942.hp1 NA19062.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 49 | chr13 | 46127542 | |||||
chr13:46127543 | G | A | 2 | a0001c0001t0010a0001c0001t0027 | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*48C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 48 | chr13 | 46127543 | |||||
chr13:46127566 | G | A | 1 | a0001c0001t0026 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 25 | chr13 | 46127566 | |||||
chr13:46127579 | C | A | 1 | a0001c0001t0027 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 16/16 | 12 | chr13 | 46127579 | |||||
chr13:46182126 | C | A | 1 | a0001c0001t0028 | 1 | NA18981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/16 | 22464 | chr13 | 46182126 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46127805 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1752-82G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46127805 | ||||||
chr13:46127903 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1752-180G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46127903 | ||||||
chr13:46127915 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1752-192G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46127915 | ||||||
chr13:46127981 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1752-258A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46127981 | ||||||
chr13:46127987 | CT | C | 152 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 155 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1752-265delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46127987 | ||||||
chr13:46128003 | G | GT | 5 | a0001c0001t0006g0276a0001c0001t0006g0305a0001c0001t0007g0005others(2): Show | 6 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1752-281dupA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128003 | ||||||
chr13:46128003 | GT | G | 137 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 139 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.1752-281delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128003 | ||||||
chr13:46128003 | GTT | G | 168 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0001t0001g0215others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1752-282_1752-281d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128003 | ||||||
chr13:46128003 | GTTT | G | 20 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0230others(17): Show | 22 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1752-283_1752-281d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128003 | ||||||
chr13:46128111 | G | T | 1 | a0001c0001t0002g0263 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1752-388C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128111 | ||||||
chr13:46128167 | A | C | 6 | a0001c0001t0006g0206a0001c0001t0006g0208a0001c0001t0009g0039others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1752-444T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128167 | ||||||
chr13:46128219 | T | C | 1 | a0001c0003t0004g0301 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1752-496A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128219 | ||||||
chr13:46128245 | CA | C | 6 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0212others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1752-523delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128245 | ||||||
chr13:46128266 | T | C | 29 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0230others(26): Show | 32 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1752-543A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128266 | ||||||
chr13:46128324 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1752-601G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128324 | ||||||
chr13:46128327 | G | A | 5 | a0001c0001t0002g0057a0001c0001t0002g0281a0001c0001t0002g0298others(2): Show | 5 | HG00323.hp1 HG00738.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-604C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128327 | ||||||
chr13:46128350 | A | G | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1752-627T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128350 | ||||||
chr13:46128356 | C | T | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1752-633G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128356 | ||||||
chr13:46128360 | T | A | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1752-637A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128360 | ||||||
chr13:46128364 | C | T | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1752-641G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128364 | ||||||
chr13:46128369 | C | T | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1752-646G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128369 | ||||||
chr13:46128370 | G | A | 139 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0283others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1752-647C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128370 | ||||||
chr13:46128373 | T | C | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1752-650A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128373 | ||||||
chr13:46128392 | A | T | 6 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0212others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1752-669T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128392 | ||||||
chr13:46128395 | G | A | 303 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(300): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1752-672C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128395 | ||||||
chr13:46128402 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1752-679A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128402 | ||||||
chr13:46128409 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1752-686G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128409 | ||||||
chr13:46128411 | A | G | 10 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0199others(7): Show | 10 | HG02451.hp1 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1752-688T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128411 | ||||||
chr13:46128467 | G | A | 343 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(340): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1752-744C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128467 | ||||||
chr13:46128468 | T | G | 2 | a0001c0001t0001g0254a0001c0003t0004g0301 | 2 | HG02735.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1752-745A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128468 | ||||||
chr13:46128470 | C | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0130a0001c0001t0001g0220 | 3 | HG00438.hp1 NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1752-747G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128470 | ||||||
chr13:46128471 | G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0254 | 2 | NA18961.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1752-748C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128471 | ||||||
chr13:46128481 | C | G | 1 | a0001c0001t0003g0216 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1752-758G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128481 | ||||||
chr13:46128523 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1752-800C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128523 | ||||||
chr13:46128547 | A | G | 1 | a0001c0001t0026g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1752-824T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128547 | ||||||
chr13:46128553 | G | A | 3 | a0001c0001t0009g0039a0001c0001t0009g0222a0001c0001t0022g0133 | 3 | HG01109.hp2 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1752-830C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128553 | ||||||
chr13:46128562 | T | C | 4 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-839A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128562 | ||||||
chr13:46128584 | T | C | 2 | a0001c0001t0002g0119a0001c0001t0002g0253 | 2 | NA18949.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1752-861A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128584 | ||||||
chr13:46128591 | C | T | 1 | a0001c0001t0022g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1752-868G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128591 | ||||||
chr13:46128599 | G | GA | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752-877dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128599 | ||||||
chr13:46128653 | C | G | 1 | a0001c0001t0001g0334 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1752-930G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128653 | ||||||
chr13:46128656 | A | T | 34 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0230others(31): Show | 37 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1752-933T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128656 | ||||||
chr13:46128703 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1752-980T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128703 | ||||||
chr13:46128771 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1752-1048G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128771 | ||||||
chr13:46128811 | T | C | 137 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1752-1088A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128811 | ||||||
chr13:46128884 | T | TACTATGG others(11): Show |
272 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1752-1179_1752-116 others(22): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128884 | ||||||
chr13:46128990 | G | C | 31 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0230others(28): Show | 33 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1752-1267C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46128990 | ||||||
chr13:46129007 | G | A | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(314): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1752-1284C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129007 | ||||||
chr13:46129104 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1752-1381C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129104 | ||||||
chr13:46129180 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1752-1457G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129180 | ||||||
chr13:46129262 | C | G | 1 | a0001c0003t0004g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1752-1539G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129262 | ||||||
chr13:46129318 | C | T | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1751+1496G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129318 | ||||||
chr13:46129351 | AC | A | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1751+1462delG | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129351 | ||||||
chr13:46129782 | G | C | 2 | a0001c0001t0011g0246a0001c0001t0011g0247 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1751+1032C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129782 | ||||||
chr13:46129854 | C | G | 2 | a0001c0001t0003g0307a0003c0006t0003g0203 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1751+960G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129854 | ||||||
chr13:46129876 | G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0199others(1): Show | 4 | HG02451.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751+938C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129876 | ||||||
chr13:46129923 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1751+891G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129923 | ||||||
chr13:46129953 | G | A | 7 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0231others(4): Show | 8 | HG01891.hp1 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1751+861C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46129953 | ||||||
chr13:46130078 | A | G | 138 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1751+736T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130078 | ||||||
chr13:46130125 | C | T | 31 | a0001c0001t0006g0095a0001c0001t0006g0097a0001c0001t0006g0204others(28): Show | 31 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1751+689G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130125 | ||||||
chr13:46130160 | T | A | 1 | a0001c0001t0026g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1751+654A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130160 | ||||||
chr13:46130233 | G | A | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1751+581C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130233 | ||||||
chr13:46130261 | G | C | 1 | a0001c0001t0006g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1751+553C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130261 | ||||||
chr13:46130487 | T | C | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1751+327A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130487 | ||||||
chr13:46130588 | G | GTTT | 6 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0212others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1751+223_1751+225d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130588 | ||||||
chr13:46130588 | GT | G | 155 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289others(152): Show | 157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1751+225delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 15/15 | chr13 | 46130588 | ||||||
chr13:46130952 | C | A | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-14G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46130952 | ||||||
chr13:46131137 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1627-199C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131137 | ||||||
chr13:46131260 | G | A | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627-322C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131260 | ||||||
chr13:46131593 | T | A | 322 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1627-655A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131593 | ||||||
chr13:46131644 | T | C | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-706A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131644 | ||||||
chr13:46131665 | T | C | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-727A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131665 | ||||||
chr13:46131708 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1627-770G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131708 | ||||||
chr13:46131717 | A | C | 7 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0231others(4): Show | 8 | HG01891.hp1 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1627-779T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131717 | ||||||
chr13:46131738 | G | C | 322 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1627-800C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131738 | ||||||
chr13:46131795 | G | C | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627-857C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131795 | ||||||
chr13:46131827 | A | C | 1 | a0001c0001t0002g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1627-889T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46131827 | ||||||
chr13:46132001 | CT | C | 40 | a0001c0001t0006g0095a0001c0001t0006g0097a0001c0001t0006g0204others(37): Show | 40 | HG00673.hp1 HG01070.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1627-1064delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132001 | ||||||
chr13:46132001 | CTT | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(312): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1627-1065_1627-106 others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132001 | ||||||
chr13:46132001 | CTTT | C | 10 | a0001c0001t0001g0148a0001c0001t0002g0221a0001c0001t0002g0256others(7): Show | 11 | HG00323.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1627-1066_1627-106 others(7): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132001 | ||||||
chr13:46132072 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1627-1134G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132072 | ||||||
chr13:46132101 | G | GTGGC | 169 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1627-1167_1627-116 others(8): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132101 | ||||||
chr13:46132300 | C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0096a0001c0001t0002g0304others(1): Show | 4 | HG02109.hp1 HG02148.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1627-1362G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132300 | ||||||
chr13:46132463 | C | A | 168 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1627-1525G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132463 | ||||||
chr13:46132531 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1627-1593C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132531 | ||||||
chr13:46132609 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1626+1518A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132609 | ||||||
chr13:46132653 | C | T | 329 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1626+1474G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132653 | ||||||
chr13:46132754 | A | G | 333 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1626+1373T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132754 | ||||||
chr13:46132791 | C | G | 138 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1626+1336G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132791 | ||||||
chr13:46132807 | C | T | 2 | a0001c0001t0002g0111a0001c0001t0002g0323 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1626+1320G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132807 | ||||||
chr13:46132929 | A | G | 138 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1626+1198T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46132929 | ||||||
chr13:46133002 | T | C | 169 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1626+1125A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133002 | ||||||
chr13:46133005 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1626+1122A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133005 | ||||||
chr13:46133101 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1626+1026T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133101 | ||||||
chr13:46133172 | A | C | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1626+955T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133172 | ||||||
chr13:46133224 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1626+903C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133224 | ||||||
chr13:46133580 | C | T | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1626+547G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133580 | ||||||
chr13:46133701 | T | A | 329 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1626+426A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133701 | ||||||
chr13:46133732 | G | A | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1626+395C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133732 | ||||||
chr13:46133771 | G | T | 7 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0231others(4): Show | 8 | HG01891.hp1 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1626+356C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133771 | ||||||
chr13:46133980 | A | T | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1626+147T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46133980 | ||||||
chr13:46134063 | A | C | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1626+64T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46134063 | ||||||
chr13:46134113 | A | G | 1 | a0001c0001t0008g0261 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1626+14T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 14/15 | chr13 | 46134113 | ||||||
chr13:46134469 | T | C | 6 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0231others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503-219A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134469 | ||||||
chr13:46134564 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1503-314G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134564 | ||||||
chr13:46134596 | C | A | 365 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(362): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1503-346G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134596 | ||||||
chr13:46134796 | T | A | 4 | a0001c0001t0003g0040a0001c0001t0003g0270a0001c0001t0003g0306others(1): Show | 4 | HG02976.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503-546A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134796 | ||||||
chr13:46134842 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1503-592C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134842 | ||||||
chr13:46134893 | C | G | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503-643G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134893 | ||||||
chr13:46134924 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1503-674G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46134924 | ||||||
chr13:46135041 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1503-791T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135041 | ||||||
chr13:46135091 | A | G | 7 | a0001c0001t0006g0097a0001c0001t0006g0204a0001c0001t0006g0206others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503-841T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135091 | ||||||
chr13:46135108 | C | CA | 179 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0024others(176): Show | 180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1503-859dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135108 | ||||||
chr13:46135124 | G | A | 158 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1503-874C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135124 | ||||||
chr13:46135125 | A | AAG | 15 | a0001c0001t0001g0132a0001c0003t0004g0001a0001c0003t0004g0002others(12): Show | 17 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1503-876_1503-875i others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135125 | ||||||
chr13:46135125 | A | G | 139 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 142 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1503-875T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135125 | ||||||
chr13:46135237 | T | G | 1 | a0001c0001t0002g0138 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1503-987A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135237 | ||||||
chr13:46135254 | T | C | 325 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1503-1004A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135254 | ||||||
chr13:46135482 | C | T | 1 | a0001c0001t0009g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1503-1232G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135482 | ||||||
chr13:46135675 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1503-1425T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135675 | ||||||
chr13:46135743 | C | CT | 128 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1503-1494dupA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135743 | ||||||
chr13:46135743 | C | CTT | 6 | a0001c0001t0001g0134a0001c0001t0001g0161a0001c0001t0001g0178others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503-1495_1503-149 others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135743 | ||||||
chr13:46135743 | CT | C | 179 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0024others(176): Show | 182 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1503-1494delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135743 | ||||||
chr13:46135940 | C | A | 1 | a0003c0006t0003g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1503-1690G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46135940 | ||||||
chr13:46136074 | T | TAC | 99 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0024others(96): Show | 100 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1503-1826_1503-182 others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | T | TACAC | 31 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1503-1828_1503-182 others(8): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | T | TACACAC | 5 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0123others(2): Show | 5 | HG00140.hp1 HG00741.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1503-1830_1503-182 others(10): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | T | TACACACA others(1): Show |
5 | a0001c0001t0002g0046a0001c0001t0006g0204a0001c0001t0006g0276others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1503-1832_1503-182 others(12): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | TAC | T | 123 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(120): Show | 124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1503-1826_1503-182 others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | TACAC | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0132others(24): Show | 30 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1503-1828_1503-182 others(8): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | TACACACA others(1): Show |
T | 10 | a0001c0001t0003g0047a0001c0001t0006g0212a0001c0001t0009g0200others(7): Show | 10 | HG02717.hp2 HG02723.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1503-1832_1503-182 others(12): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | TACACACA others(3): Show |
T | 1 | a0001c0001t0007g0231 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1503-1834_1503-182 others(14): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136074 | TACACACA others(5): Show |
T | 24 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0059others(21): Show | 24 | HG01074.hp2 HG01106.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1503-1836_1503-182 others(16): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136074 | ||||||
chr13:46136138 | A | G | 1 | a0001c0001t0026g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1503-1888T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136138 | ||||||
chr13:46136177 | C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0325 | 2 | HG01433.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1503-1927G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136177 | ||||||
chr13:46136353 | G | T | 5 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0240others(2): Show | 6 | HG02257.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503-2103C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136353 | ||||||
chr13:46136462 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1503-2212C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136462 | ||||||
chr13:46136741 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1503-2491C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136741 | ||||||
chr13:46136745 | A | G | 4 | a0001c0001t0006g0206a0001c0001t0006g0212a0001c0001t0009g0200others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503-2495T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136745 | ||||||
chr13:46136972 | A | G | 2 | a0002c0002t0016g0191a0002c0002t0016g0311 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1503-2722T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46136972 | ||||||
chr13:46137209 | TA | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(156): Show | 161 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1503-2960delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137209 | ||||||
chr13:46137224 | A | AAC | 21 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(18): Show | 21 | HG01074.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1503-2975_1503-297 others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137224 | ||||||
chr13:46137224 | A | AC | 3 | a0001c0001t0009g0039a0001c0001t0009g0222a0001c0001t0022g0133 | 3 | HG01109.hp2 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1503-2975dupG | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137224 | ||||||
chr13:46137224 | A | C | 5 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0240others(2): Show | 6 | HG02257.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503-2974T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137224 | ||||||
chr13:46137266 | G | C | 1 | a0001c0001t0022g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1503-3016C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137266 | ||||||
chr13:46137308 | C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289 | 3 | HG02074.hp2 NA18970.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1503-3058G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137308 | ||||||
chr13:46137312 | C | T | 55 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(52): Show | 58 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1503-3062G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137312 | ||||||
chr13:46137366 | T | C | 1 | a0001c0001t0006g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1503-3116A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137366 | ||||||
chr13:46137401 | G | A | 1 | a0002c0002t0003g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1503-3151C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137401 | ||||||
chr13:46137432 | T | C | 4 | a0001c0001t0006g0206a0001c0001t0006g0212a0001c0001t0009g0200others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503-3182A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137432 | ||||||
chr13:46137467 | C | T | 1 | a0001c0001t0025g0173 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1503-3217G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137467 | ||||||
chr13:46137498 | C | T | 139 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1503-3248G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137498 | ||||||
chr13:46137615 | T | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0033others(4): Show | 7 | NA18949.hp1 NA18949.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1503-3365A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137615 | ||||||
chr13:46137657 | T | G | 1 | a0001c0001t0002g0113 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1503-3407A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137657 | ||||||
chr13:46137821 | C | A | 3 | a0001c0001t0003g0216a0001c0001t0003g0307a0003c0006t0003g0203 | 3 | HG02109.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1503-3571G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137821 | ||||||
chr13:46137837 | C | T | 60 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(57): Show | 63 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.1503-3587G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137837 | ||||||
chr13:46137911 | A | G | 1 | a0002c0002t0003g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1503-3661T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46137911 | ||||||
chr13:46138029 | A | T | 60 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(57): Show | 63 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.1503-3779T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138029 | ||||||
chr13:46138052 | T | C | 1 | a0001c0001t0013g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1503-3802A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138052 | ||||||
chr13:46138230 | T | G | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1503-3980A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138230 | ||||||
chr13:46138242 | TA | T | 59 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(56): Show | 62 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.1503-3993delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138242 | ||||||
chr13:46138313 | T | C | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+3979A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138313 | ||||||
chr13:46138339 | A | G | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+3953T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138339 | ||||||
chr13:46138366 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1502+3926G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138366 | ||||||
chr13:46138421 | TTCTG | T | 7 | a0001c0001t0002g0177a0001c0001t0002g0180a0001c0001t0002g0181others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502+3867_1502+387 others(8): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138421 | ||||||
chr13:46138445 | G | A | 1 | a0001c0001t0008g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1502+3847C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138445 | ||||||
chr13:46138452 | A | G | 365 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(362): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1502+3840T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138452 | ||||||
chr13:46138632 | G | A | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+3660C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138632 | ||||||
chr13:46138739 | C | A | 5 | a0001c0001t0007g0005a0001c0001t0007g0209a0001c0001t0007g0240others(2): Show | 6 | HG02257.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1502+3553G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138739 | ||||||
chr13:46138782 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1502+3510C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138782 | ||||||
chr13:46138917 | G | T | 4 | a0001c0001t0006g0206a0001c0001t0006g0212a0001c0001t0009g0200others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502+3375C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138917 | ||||||
chr13:46138941 | C | T | 1 | a0001c0003t0004g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1502+3351G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138941 | ||||||
chr13:46138974 | A | G | 1 | a0001c0001t0025g0173 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1502+3318T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46138974 | ||||||
chr13:46139173 | A | G | 29 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(26): Show | 29 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1502+3119T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139173 | ||||||
chr13:46139459 | T | C | 1 | a0001c0001t0002g0345 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1502+2833A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139459 | ||||||
chr13:46139504 | T | G | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+2788A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139504 | ||||||
chr13:46139567 | G | A | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+2725C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139567 | ||||||
chr13:46139690 | T | C | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+2602A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139690 | ||||||
chr13:46139860 | G | C | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+2432C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139860 | ||||||
chr13:46139903 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1502+2389C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139903 | ||||||
chr13:46139904 | C | A | 63 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(60): Show | 66 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1502+2388G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139904 | ||||||
chr13:46139973 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1502+2319C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46139973 | ||||||
chr13:46140043 | A | G | 1 | a0002c0002t0003g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1502+2249T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140043 | ||||||
chr13:46140324 | G | A | 1 | a0001c0001t0004g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1502+1968C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140324 | ||||||
chr13:46140579 | C | T | 3 | a0001c0003t0004g0002a0001c0003t0004g0160a0001c0003t0004g0224 | 4 | HG01257.hp1 HG01346.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502+1713G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140579 | ||||||
chr13:46140750 | C | A | 203 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1502+1542G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140750 | ||||||
chr13:46140879 | G | C | 1 | a0001c0001t0009g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1502+1413C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140879 | ||||||
chr13:46140941 | G | A | 2 | a0001c0001t0002g0004a0001c0001t0002g0214 | 3 | HG01884.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1502+1351C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140941 | ||||||
chr13:46140965 | C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0251 | 2 | NA18988.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1502+1327G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46140965 | ||||||
chr13:46141084 | T | C | 203 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1502+1208A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141084 | ||||||
chr13:46141134 | A | G | 203 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1502+1158T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141134 | ||||||
chr13:46141155 | C | A | 2 | a0002c0002t0003g0089a0002c0002t0003g0232 | 2 | NA18941.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1502+1137G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141155 | ||||||
chr13:46141208 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1502+1084G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141208 | ||||||
chr13:46141384 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1502+908G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141384 | ||||||
chr13:46141405 | C | CA | 32 | a0001c0001t0001g0038a0001c0001t0001g0117a0001c0001t0001g0132others(29): Show | 34 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1502+886dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141405 | ||||||
chr13:46141405 | C | CAA | 107 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(104): Show | 110 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1502+885_1502+886d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141405 | ||||||
chr13:46141405 | C | CAAA | 41 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0027others(38): Show | 42 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1502+884_1502+886d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141405 | ||||||
chr13:46141477 | G | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(151): Show | 158 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1502+815C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141477 | ||||||
chr13:46141481 | T | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(151): Show | 158 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1502+811A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141481 | ||||||
chr13:46141519 | G | A | 2 | a0002c0002t0016g0191a0002c0002t0016g0311 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1502+773C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141519 | ||||||
chr13:46141610 | C | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0171a0001c0001t0001g0278others(6): Show | 9 | HG00733.hp2 HG00735.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1502+682G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141610 | ||||||
chr13:46141614 | C | G | 1 | a0001c0001t0002g0273 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1502+678G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141614 | ||||||
chr13:46141941 | T | C | 21 | a0001c0001t0001g0132a0001c0001t0010g0280a0001c0001t0010g0314others(18): Show | 23 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1502+351A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46141941 | ||||||
chr13:46142001 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1502+291A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46142001 | ||||||
chr13:46142019 | A | T | 1 | a0001c0001t0004g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1502+273T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46142019 | ||||||
chr13:46142028 | T | C | 49 | a0001c0001t0001g0132a0001c0001t0003g0047a0001c0001t0003g0216others(46): Show | 51 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1502+264A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46142028 | ||||||
chr13:46142095 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1502+197T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46142095 | ||||||
chr13:46142129 | G | A | 352 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(349): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1502+163C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 13/15 | chr13 | 46142129 | ||||||
chr13:46142548 | T | C | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1369-123A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 12/15 | chr13 | 46142548 | ||||||
chr13:46142666 | A | G | 1 | a0001c0001t0006g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1369-241T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 12/15 | chr13 | 46142666 | ||||||
chr13:46142912 | T | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 142 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1368+378A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 12/15 | chr13 | 46142912 | ||||||
chr13:46143065 | A | C | 1 | a0001c0001t0002g0345 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1368+225T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 12/15 | chr13 | 46143065 | ||||||
chr13:46143111 | T | C | 203 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1368+179A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 12/15 | chr13 | 46143111 | ||||||
chr13:46143202 | C | A | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1368+88G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 12/15 | chr13 | 46143202 | ||||||
chr13:46143535 | C | T | 1 | a0001c0003t0004g0302 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1254-131G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143535 | ||||||
chr13:46143662 | C | T | 2 | a0001c0001t0001g0070a0001c0001t0002g0268 | 2 | HG02004.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1254-258G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143662 | ||||||
chr13:46143804 | C | T | 1 | a0001c0001t0009g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1254-400G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143804 | ||||||
chr13:46143805 | G | A | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1254-401C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143805 | ||||||
chr13:46143838 | G | A | 1 | a0002c0002t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1254-434C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143838 | ||||||
chr13:46143862 | C | T | 1 | a0001c0003t0004g0335 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1254-458G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143862 | ||||||
chr13:46143863 | A | G | 63 | a0001c0001t0001g0132a0001c0001t0002g0004a0001c0001t0003g0047others(60): Show | 67 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1254-459T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143863 | ||||||
chr13:46143947 | T | C | 5 | a0001c0001t0002g0004a0001c0001t0007g0005a0001c0001t0007g0209others(2): Show | 7 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1253+495A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143947 | ||||||
chr13:46143948 | C | T | 1 | a0001c0001t0001g0369 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1253+494G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143948 | ||||||
chr13:46143981 | G | T | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253+461C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143981 | ||||||
chr13:46143983 | G | A | 7 | a0001c0001t0002g0177a0001c0001t0002g0180a0001c0001t0002g0181others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1253+459C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46143983 | ||||||
chr13:46144091 | A | G | 23 | a0001c0001t0001g0132a0001c0001t0004g0227a0001c0001t0004g0228others(20): Show | 25 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1253+351T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46144091 | ||||||
chr13:46144366 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1253+76G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46144366 | ||||||
chr13:46144368 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1253+74A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46144368 | ||||||
chr13:46144372 | G | C | 1 | a0001c0001t0002g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1253+70C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46144372 | ||||||
chr13:46144402 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1253+40A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 11/15 | chr13 | 46144402 | ||||||
chr13:46144587 | T | C | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1175-67A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46144587 | ||||||
chr13:46144867 | A | G | 2 | a0001c0001t0006g0095a0001c0001t0006g0208 | 2 | HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1175-347T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46144867 | ||||||
chr13:46144879 | AATTGAGA others(29): Show |
A | 1 | a0001c0001t0028g0374 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1175-395_1175-360d others(38): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46144879 | ||||||
chr13:46144881 | T | A | 1 | a0001c0001t0002g0004 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1175-361A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46144881 | ||||||
chr13:46144886 | A | T | 2 | a0001c0001t0006g0095a0001c0001t0006g0208 | 2 | HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1175-366T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46144886 | ||||||
chr13:46145014 | G | C | 7 | a0001c0001t0002g0004a0001c0001t0007g0005a0001c0001t0007g0209others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175-494C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145014 | ||||||
chr13:46145021 | G | A | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1175-501C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145021 | ||||||
chr13:46145136 | A | G | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1175-616T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145136 | ||||||
chr13:46145156 | A | G | 18 | a0001c0001t0001g0132a0001c0001t0026g0184a0001c0003t0004g0001others(15): Show | 20 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1175-636T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145156 | ||||||
chr13:46145399 | C | G | 1 | a0001c0001t0011g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-879G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145399 | ||||||
chr13:46145616 | TAAAAGAG others(319): Show |
T | 78 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0070others(75): Show | 82 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1174+966_1175-1097 others(3): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145616 | ||||||
chr13:46145800 | T | C | 150 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0024others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1174+1108A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145800 | ||||||
chr13:46145836 | G | C | 1 | a0001c0001t0002g0300 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1174+1072C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145836 | ||||||
chr13:46145908 | C | CA | 19 | a0001c0001t0001g0049a0001c0001t0001g0168a0001c0001t0001g0199others(16): Show | 19 | HG00642.hp1 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1174+999dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CA | C | 83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(80): Show | 84 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1174+999delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAA | C | 90 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0021others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1174+998_1174+999d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAA | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0101others(21): Show | 25 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1174+997_1174+999d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAA | C | 21 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(18): Show | 21 | HG00140.hp1 HG01069.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1174+996_1174+999d others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1174+990_1174+999d others(12): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1174+988_1174+999d others(14): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0107 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1174+987_1174+999d others(15): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0150a0001c0001t0002g0298 | 2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1174+985_1174+999d others(17): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0002g0111a0001c0001t0002g0323a0001c0001t0019g0055 | 3 | HG03688.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1174+984_1174+999d others(18): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1174+983_1174+999d others(19): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145908 | CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0001g0369a0001c0001t0002g0114a0001c0001t0003g0040 | 3 | HG02976.hp2 NA18975.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1174+982_1174+999d others(20): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145908 | ||||||
chr13:46145914 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1174+994T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145914 | ||||||
chr13:46145956 | C | T | 36 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0070others(33): Show | 38 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1174+952G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46145956 | ||||||
chr13:46146031 | G | A | 1 | a0001c0001t0006g0116 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1174+877C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146031 | ||||||
chr13:46146292 | G | A | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1174+616C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146292 | ||||||
chr13:46146313 | G | C | 2 | a0001c0001t0001g0042a0001c0001t0018g0152 | 2 | HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1174+595C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146313 | ||||||
chr13:46146335 | A | T | 1 | a0002c0002t0003g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1174+573T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146335 | ||||||
chr13:46146342 | T | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1174+566A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146342 | ||||||
chr13:46146598 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1174+310G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146598 | ||||||
chr13:46146659 | C | T | 1 | a0001c0005t0001g0154 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1174+249G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146659 | ||||||
chr13:46146706 | G | A | 7 | a0001c0001t0002g0004a0001c0001t0007g0005a0001c0001t0007g0209others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174+202C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 10/15 | chr13 | 46146706 | ||||||
chr13:46147334 | A | T | 1 | a0001c0001t0002g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.979-231T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147334 | ||||||
chr13:46147407 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.979-304A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147407 | ||||||
chr13:46147427 | C | A | 36 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0070others(33): Show | 38 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.979-324G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147427 | ||||||
chr13:46147445 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.979-342T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147445 | ||||||
chr13:46147485 | A | C | 1 | a0001c0001t0002g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.979-382T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147485 | ||||||
chr13:46147599 | C | T | 7 | a0001c0001t0002g0004a0001c0001t0007g0005a0001c0001t0007g0209others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.979-496G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147599 | ||||||
chr13:46147634 | T | C | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-531A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147634 | ||||||
chr13:46147889 | A | T | 3 | a0001c0001t0002g0326a0001c0001t0014g0275a0001c0001t0014g0365 | 3 | HG02056.hp1 HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.978+463T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147889 | ||||||
chr13:46147900 | T | G | 25 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(22): Show | 25 | HG01074.hp2 HG01884.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.978+452A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147900 | ||||||
chr13:46147926 | C | T | 1 | a0005c0012t0002g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.978+426G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46147926 | ||||||
chr13:46148114 | T | G | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.978+238A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46148114 | ||||||
chr13:46148223 | C | T | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+129G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46148223 | ||||||
chr13:46148255 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.978+97C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46148255 | ||||||
chr13:46148255 | G | C | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.978+97C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46148255 | ||||||
chr13:46148291 | T | C | 7 | a0001c0001t0002g0004a0001c0001t0007g0005a0001c0001t0007g0209others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.978+61A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46148291 | ||||||
chr13:46148308 | A | C | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.978+44T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 9/15 | chr13 | 46148308 | ||||||
chr13:46148568 | C | CTTAA | 201 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(198): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.883-125_883-122dup others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148568 | ||||||
chr13:46148755 | A | G | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-308T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148755 | ||||||
chr13:46148769 | A | AAT | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-324_883-323dup others(2): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148769 | ||||||
chr13:46148822 | A | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0131a0001c0001t0001g0264 | 3 | NA18979.hp2 NA18991.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.883-375T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148822 | ||||||
chr13:46148889 | C | T | 1 | a0001c0003t0004g0166 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.883-442G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148889 | ||||||
chr13:46148937 | C | T | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.883-490G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148937 | ||||||
chr13:46148973 | G | A | 28 | a0001c0001t0003g0047a0001c0001t0003g0216a0001c0001t0003g0307others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.883-526C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46148973 | ||||||
chr13:46149032 | T | C | 1 | a0001c0001t0023g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.883-585A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149032 | ||||||
chr13:46149133 | T | C | 1 | a0002c0002t0005g0360 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.883-686A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149133 | ||||||
chr13:46149159 | T | A | 161 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.883-712A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149159 | ||||||
chr13:46149238 | G | A | 5 | a0002c0002t0003g0245a0002c0002t0003g0248a0002c0002t0003g0249others(2): Show | 5 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-791C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149238 | ||||||
chr13:46149459 | T | C | 203 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.883-1012A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149459 | ||||||
chr13:46149487 | A | C | 1 | a0001c0001t0002g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.883-1040T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149487 | ||||||
chr13:46149580 | A | G | 360 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(357): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.883-1133T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149580 | ||||||
chr13:46149648 | G | A | 1 | a0002c0002t0003g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.883-1201C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149648 | ||||||
chr13:46149978 | A | G | 125 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.882+958T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46149978 | ||||||
chr13:46150031 | C | T | 145 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0033others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.882+905G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150031 | ||||||
chr13:46150112 | T | C | 3 | a0001c0001t0006g0212a0001c0001t0009g0200a0001c0001t0009g0303 | 3 | HG02717.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882+824A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150112 | ||||||
chr13:46150249 | T | G | 2 | a0001c0001t0003g0307a0003c0006t0003g0203 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.882+687A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150249 | ||||||
chr13:46150285 | T | C | 3 | a0001c0003t0004g0002a0001c0003t0004g0160a0001c0003t0004g0224 | 4 | HG01257.hp1 HG01346.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+651A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150285 | ||||||
chr13:46150466 | A | G | 2 | a0001c0001t0002g0017a0001c0003t0004g0302 | 2 | HG01516.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.882+470T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150466 | ||||||
chr13:46150636 | T | G | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+300A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150636 | ||||||
chr13:46150720 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882+216A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150720 | ||||||
chr13:46150742 | T | C | 1 | a0001c0001t0002g0020 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.882+194A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150742 | ||||||
chr13:46150759 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.882+177C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150759 | ||||||
chr13:46150804 | C | A | 1 | a0001c0001t0002g0273 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.882+132G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 8/15 | chr13 | 46150804 | ||||||
chr13:46151127 | GA | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0070others(10): Show | 13 | HG00642.hp2 HG01123.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.740-50delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151127 | ||||||
chr13:46151134 | G | T | 1 | a0001c0001t0007g0240 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.740-56C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151134 | ||||||
chr13:46151135 | T | C | 5 | a0001c0001t0010g0280a0001c0001t0010g0314a0001c0001t0010g0338others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-57A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151135 | ||||||
chr13:46151260 | G | A | 29 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0034others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.740-182C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151260 | ||||||
chr13:46151421 | A | G | 47 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0070others(44): Show | 51 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.740-343T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151421 | ||||||
chr13:46151516 | A | G | 6 | a0001c0001t0003g0216a0002c0002t0001g0308a0002c0002t0001g0331others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-438T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151516 | ||||||
chr13:46151702 | T | G | 7 | a0001c0001t0002g0004a0001c0001t0006g0212a0001c0001t0007g0005others(4): Show | 9 | HG01891.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-624A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151702 | ||||||
chr13:46151791 | A | G | 2 | a0001c0001t0009g0039a0001c0001t0009g0222 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.740-713T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151791 | ||||||
chr13:46151946 | C | T | 1 | a0001c0001t0002g0332 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.739+834G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151946 | ||||||
chr13:46151947 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.739+833C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46151947 | ||||||
chr13:46152286 | C | T | 5 | a0001c0001t0002g0075a0001c0001t0002g0113a0001c0001t0002g0170others(2): Show | 5 | HG00621.hp1 NA18952.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.739+494G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152286 | ||||||
chr13:46152290 | C | T | 6 | a0001c0001t0002g0259a0001c0001t0010g0280a0001c0001t0010g0314others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+490G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152290 | ||||||
chr13:46152408 | T | C | 1 | a0001c0001t0026g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.739+372A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152408 | ||||||
chr13:46152495 | G | C | 1 | a0001c0001t0002g0332 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.739+285C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152495 | ||||||
chr13:46152552 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.739+228T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152552 | ||||||
chr13:46152557 | C | A | 1 | a0002c0002t0016g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.739+223G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152557 | ||||||
chr13:46152728 | C | T | 11 | a0001c0001t0002g0081a0001c0001t0002g0336a0001c0001t0003g0320others(8): Show | 11 | HG02258.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.739+52G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 7/15 | chr13 | 46152728 | ||||||
chr13:46153036 | C | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0185 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.574-91G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153036 | ||||||
chr13:46153270 | T | C | 359 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(356): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.574-325A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153270 | ||||||
chr13:46153443 | A | G | 1 | a0001c0003t0004g0301 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.574-498T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153443 | ||||||
chr13:46153450 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.574-505G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153450 | ||||||
chr13:46153473 | G | T | 18 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0254others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.574-528C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153473 | ||||||
chr13:46153474 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.574-529C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153474 | ||||||
chr13:46153539 | A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0185 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.574-594T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153539 | ||||||
chr13:46153584 | C | T | 2 | a0001c0001t0015g0324a0001c0001t0015g0346 | 2 | HG02083.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.574-639G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153584 | ||||||
chr13:46153648 | C | G | 2 | a0001c0001t0015g0324a0001c0001t0015g0346 | 2 | HG02083.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.574-703G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153648 | ||||||
chr13:46153753 | CTG | C | 18 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0254others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.574-810_574-809del others(2): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153753 | ||||||
chr13:46153859 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.574-914C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46153859 | ||||||
chr13:46154036 | T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0344 | 2 | HG00735.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.573+769A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154036 | ||||||
chr13:46154050 | A | C | 1 | a0001c0001t0025g0173 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.573+755T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154050 | ||||||
chr13:46154080 | G | A | 4 | a0001c0001t0002g0213a0001c0001t0013g0016a0001c0001t0013g0202others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+725C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154080 | ||||||
chr13:46154111 | A | G | 1 | a0002c0002t0001g0331 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.573+694T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154111 | ||||||
chr13:46154390 | T | G | 46 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0044others(43): Show | 48 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.573+415A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154390 | ||||||
chr13:46154402 | G | A | 2 | a0001c0005t0001g0154a0001c0005t0001g0169 | 2 | NA18946.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.573+403C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154402 | ||||||
chr13:46154448 | T | C | 173 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(170): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.573+357A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154448 | ||||||
chr13:46154453 | C | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0033others(12): Show | 15 | HG00558.hp1 HG00673.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+352G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154453 | ||||||
chr13:46154462 | G | A | 6 | a0001c0001t0002g0081a0001c0001t0007g0240a0001c0001t0011g0235others(3): Show | 6 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+343C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154462 | ||||||
chr13:46154523 | T | C | 2 | a0001c0001t0003g0216a0001c0001t0022g0133 | 2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.573+282A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154523 | ||||||
chr13:46154590 | C | G | 1 | a0001c0003t0004g0301 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.573+215G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154590 | ||||||
chr13:46154596 | T | C | 8 | a0001c0001t0001g0070a0001c0001t0001g0146a0001c0001t0001g0274others(5): Show | 9 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+209A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154596 | ||||||
chr13:46154636 | T | C | 219 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0019others(216): Show | 223 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.573+169A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154636 | ||||||
chr13:46154681 | T | A | 5 | a0001c0001t0001g0220a0001c0001t0002g0065a0001c0001t0008g0233others(2): Show | 5 | NA18941.hp2 NA18979.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+124A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154681 | ||||||
chr13:46154789 | C | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.573+16G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 6/15 | chr13 | 46154789 | ||||||
chr13:46154899 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.492-13G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46154899 | ||||||
chr13:46154977 | A | C | 18 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0254others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.492-91T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46154977 | ||||||
chr13:46155048 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.492-162T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155048 | ||||||
chr13:46155124 | C | T | 138 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0021others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.492-238G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155124 | ||||||
chr13:46155281 | T | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0207 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.492-395A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155281 | ||||||
chr13:46155297 | T | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.492-411A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155297 | ||||||
chr13:46155308 | C | T | 1 | a0001c0001t0006g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.492-422G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155308 | ||||||
chr13:46155335 | A | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0009g0200others(1): Show | 4 | HG01975.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-449T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155335 | ||||||
chr13:46155699 | A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0289 | 3 | HG02074.hp2 NA18970.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.491+739T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155699 | ||||||
chr13:46155979 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.491+459A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46155979 | ||||||
chr13:46156030 | C | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0283a0001c0003t0004g0001others(1): Show | 5 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.491+408G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156030 | ||||||
chr13:46156093 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.491+345A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156093 | ||||||
chr13:46156148 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.491+290G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156148 | ||||||
chr13:46156158 | A | T | 1 | a0001c0001t0002g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.491+280T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156158 | ||||||
chr13:46156166 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.491+272A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156166 | ||||||
chr13:46156215 | T | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.491+223A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156215 | ||||||
chr13:46156372 | C | T | 18 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0254others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.491+66G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156372 | ||||||
chr13:46156422 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.491+16T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 5/15 | chr13 | 46156422 | ||||||
chr13:46156671 | G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0185 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.359-101C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156671 | ||||||
chr13:46156811 | GTTTCT | G | 15 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0313others(12): Show | 15 | HG00639.hp2 HG01070.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.359-246_359-242del others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156811 | ||||||
chr13:46156825 | C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.359-255G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156825 | ||||||
chr13:46156825 | CT | C | 6 | a0001c0001t0001g0146a0001c0001t0001g0266a0001c0001t0002g0020others(3): Show | 6 | HG01256.hp2 HG01975.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-256delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156825 | ||||||
chr13:46156874 | T | G | 94 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0024others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.359-304A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156874 | ||||||
chr13:46156891 | G | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0003g0216 | 3 | HG02572.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.359-321C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156891 | ||||||
chr13:46156917 | T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0207 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.359-347A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156917 | ||||||
chr13:46156969 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.359-399G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46156969 | ||||||
chr13:46157075 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-505G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157075 | ||||||
chr13:46157115 | C | A | 17 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0002g0010others(14): Show | 17 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.359-545G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157115 | ||||||
chr13:46157257 | C | CAT | 91 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0024others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.359-689_359-688dup others(2): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157257 | ||||||
chr13:46157257 | C | CATAT | 3 | a0001c0001t0001g0193a0001c0001t0003g0040a0001c0001t0009g0039 | 3 | HG01192.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.359-691_359-688dup others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157257 | ||||||
chr13:46157287 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-717A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157287 | ||||||
chr13:46157389 | T | G | 6 | a0001c0001t0003g0320a0001c0001t0006g0095a0001c0001t0006g0097others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-819A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157389 | ||||||
chr13:46157600 | T | C | 129 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0021others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.358+922A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157600 | ||||||
chr13:46157618 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.358+904A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157618 | ||||||
chr13:46157655 | G | A | 7 | a0002c0002t0005g0003a0002c0002t0005g0072a0002c0002t0005g0129others(4): Show | 8 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+867C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157655 | ||||||
chr13:46157732 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.358+790T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157732 | ||||||
chr13:46157741 | C | CT | 51 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0042others(48): Show | 52 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.358+780dupA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157741 | ||||||
chr13:46157741 | CT | C | 31 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0092others(28): Show | 31 | HG00733.hp2 HG01167.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.358+780delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157741 | ||||||
chr13:46157741 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0003g0040a0001c0001t0009g0039 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.358+769_358+780del others(12): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157741 | ||||||
chr13:46157790 | A | C | 1 | a0001c0003t0004g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.358+732T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157790 | ||||||
chr13:46157817 | G | A | 18 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0254others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.358+705C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157817 | ||||||
chr13:46157839 | T | C | 4 | a0001c0001t0003g0022a0001c0001t0003g0087a0001c0001t0003g0099others(1): Show | 4 | HG03225.hp1 NA18970.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+683A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157839 | ||||||
chr13:46157844 | T | C | 1 | a0001c0001t0002g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.358+678A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157844 | ||||||
chr13:46157858 | T | C | 151 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0021others(148): Show | 153 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.358+664A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157858 | ||||||
chr13:46157870 | C | A | 8 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0196others(5): Show | 8 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+652G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46157870 | ||||||
chr13:46158018 | T | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0168others(34): Show | 37 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.358+504A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46158018 | ||||||
chr13:46158034 | T | C | 131 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(128): Show | 133 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.358+488A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46158034 | ||||||
chr13:46158123 | T | C | 1 | a0002c0002t0016g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.358+399A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46158123 | ||||||
chr13:46158193 | T | C | 1 | a0001c0001t0009g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.358+329A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46158193 | ||||||
chr13:46158236 | A | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.358+286T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46158236 | ||||||
chr13:46158317 | C | A | 6 | a0001c0001t0011g0246a0001c0001t0011g0247a0002c0002t0003g0245others(3): Show | 6 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+205G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 4/15 | chr13 | 46158317 | ||||||
chr13:46158705 | A | G | 2 | a0001c0001t0002g0096a0001c0001t0002g0304 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.229-54T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 3/15 | chr13 | 46158705 | ||||||
chr13:46158713 | G | T | 1 | a0002c0002t0005g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.229-62C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 3/15 | chr13 | 46158713 | ||||||
chr13:46158743 | G | A | 1 | a0001c0003t0004g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.228+83C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 3/15 | chr13 | 46158743 | ||||||
chr13:46159100 | A | G | 132 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.65-111T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 2/15 | chr13 | 46159100 | ||||||
chr13:46159105 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-116T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 2/15 | chr13 | 46159105 | ||||||
chr13:46159105 | A | G | 56 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0001g0145others(53): Show | 57 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.65-116T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 2/15 | chr13 | 46159105 | ||||||
chr13:46159478 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+121T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 2/15 | chr13 | 46159478 | ||||||
chr13:46159488 | G | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+111C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 2/15 | chr13 | 46159488 | ||||||
chr13:46159788 | C | A | 2 | a0001c0001t0001g0254a0001c0001t0002g0252 | 2 | NA18959.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-24-102G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46159788 | ||||||
chr13:46160002 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-24-316T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160002 | ||||||
chr13:46160035 | C | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0177others(6): Show | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-349G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160035 | ||||||
chr13:46160072 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-24-386G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160072 | ||||||
chr13:46160266 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-24-580T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160266 | ||||||
chr13:46160432 | C | G | 1 | a0001c0001t0002g0077 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-24-746G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160432 | ||||||
chr13:46160553 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-867A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160553 | ||||||
chr13:46160754 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-1068C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46160754 | ||||||
chr13:46161017 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-1331C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161017 | ||||||
chr13:46161267 | C | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-1581G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161267 | ||||||
chr13:46161290 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-1604T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161290 | ||||||
chr13:46161310 | T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0283a0001c0003t0004g0001 | 4 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-1624A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161310 | ||||||
chr13:46161313 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-1627T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161313 | ||||||
chr13:46161384 | A | G | 2 | a0001c0001t0003g0040a0001c0001t0009g0039 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-1698T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161384 | ||||||
chr13:46161542 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-24-1856A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161542 | ||||||
chr13:46161569 | T | C | 3 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0211 | 3 | HG00438.hp2 HG02080.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-24-1883A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161569 | ||||||
chr13:46161785 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2099G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161785 | ||||||
chr13:46161884 | G | A | 1 | a0002c0002t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-24-2198C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161884 | ||||||
chr13:46161942 | C | G | 6 | a0001c0001t0003g0320a0001c0001t0006g0095a0001c0001t0006g0097others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-2256G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161942 | ||||||
chr13:46161945 | G | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0192 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-24-2259C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161945 | ||||||
chr13:46161961 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2275T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46161961 | ||||||
chr13:46162170 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2484G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162170 | ||||||
chr13:46162185 | C | T | 3 | a0001c0001t0002g0290a0001c0001t0012g0159a0001c0001t0012g0362 | 3 | NA18942.hp1 NA19012.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-24-2499G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162185 | ||||||
chr13:46162219 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2533A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162219 | ||||||
chr13:46162246 | TCTCCCTC others(9): Show |
T | 2 | a0001c0001t0003g0040a0001c0001t0009g0039 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-2576_-24-2561d others(18): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162246 | ||||||
chr13:46162254 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2568G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162254 | ||||||
chr13:46162254 | CCCCTCCC others(3): Show |
C | 1 | a0001c0001t0002g0083 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-24-2578_-24-2569d others(12): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162254 | ||||||
chr13:46162258 | T | TC | 6 | a0001c0001t0001g0044a0001c0001t0001g0076a0001c0001t0002g0058others(3): Show | 6 | HG01099.hp1 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-2573dupG | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162258 | ||||||
chr13:46162268 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2582A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162268 | ||||||
chr13:46162270 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2584G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162270 | ||||||
chr13:46162284 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2598A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162284 | ||||||
chr13:46162293 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2607A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162293 | ||||||
chr13:46162300 | A | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2614T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162300 | ||||||
chr13:46162304 | A | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2618T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162304 | ||||||
chr13:46162306 | G | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2620C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162306 | ||||||
chr13:46162307 | G | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2621C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162307 | ||||||
chr13:46162319 | C | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2633G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162319 | ||||||
chr13:46162324 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2638A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162324 | ||||||
chr13:46162325 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2639A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162325 | ||||||
chr13:46162330 | C | T | 2 | a0001c0001t0001g0100a0002c0002t0006g0104 | 2 | HG02071.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-24-2644G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162330 | ||||||
chr13:46162332 | T | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2646A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162332 | ||||||
chr13:46162417 | A | C | 2 | a0001c0001t0002g0041a0001c0001t0002g0052 | 2 | HG01081.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-24-2731T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162417 | ||||||
chr13:46162444 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2758G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162444 | ||||||
chr13:46162447 | G | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG02683.hp2 HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-24-2761C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162447 | ||||||
chr13:46162456 | G | C | 347 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(344): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-24-2770C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162456 | ||||||
chr13:46162510 | C | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0267 | 2 | NA18952.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-24-2824G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162510 | ||||||
chr13:46162543 | C | G | 2 | a0001c0001t0002g0010a0001c0001t0009g0222 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-24-2857G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162543 | ||||||
chr13:46162561 | G | C | 131 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-24-2875C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162561 | ||||||
chr13:46162570 | G | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-2884C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162570 | ||||||
chr13:46162623 | G | A | 6 | a0001c0001t0003g0320a0001c0001t0006g0095a0001c0001t0006g0097others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-2937C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162623 | ||||||
chr13:46162636 | A | G | 6 | a0001c0001t0003g0320a0001c0001t0006g0095a0001c0001t0006g0097others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-2950T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162636 | ||||||
chr13:46162645 | A | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0168others(9): Show | 12 | HG01109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-24-2959T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162645 | ||||||
chr13:46162713 | A | C | 1 | a0001c0001t0007g0240 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-24-3027T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162713 | ||||||
chr13:46162713 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3027T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162713 | ||||||
chr13:46162725 | T | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3039A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162725 | ||||||
chr13:46162752 | T | C | 71 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-24-3066A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162752 | ||||||
chr13:46162795 | C | T | 1 | a0002c0002t0005g0360 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-24-3109G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162795 | ||||||
chr13:46162800 | C | T | 1 | a0002c0002t0003g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-24-3114G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162800 | ||||||
chr13:46162832 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-24-3146G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162832 | ||||||
chr13:46162855 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-24-3169C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162855 | ||||||
chr13:46162859 | G | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0026g0184 | 3 | HG02895.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-24-3173C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162859 | ||||||
chr13:46162867 | A | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3181T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162867 | ||||||
chr13:46162877 | CGTCTGAG others(33): Show |
C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3231_-24-3192d others(42): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162877 | ||||||
chr13:46162882 | G | A | 1 | a0001c0001t0022g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-24-3196C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162882 | ||||||
chr13:46162908 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-24-3222G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162908 | ||||||
chr13:46162942 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3256C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162942 | ||||||
chr13:46162985 | CGGCAGCC others(63): Show |
C | 1 | a0001c0003t0004g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-24-3369_-24-3300d others(72): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162985 | ||||||
chr13:46162987 | GCAGCCGC others(39): Show |
G | 18 | a0001c0001t0001g0091a0001c0001t0001g0215a0001c0001t0001g0254others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-24-3347_-24-3302d others(48): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46162987 | ||||||
chr13:46163043 | C | T | 37 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0168others(34): Show | 38 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.-24-3357G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163043 | ||||||
chr13:46163047 | C | T | 1 | a0001c0008t0002g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-24-3361G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163047 | ||||||
chr13:46163120 | A | AC | 30 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0024others(27): Show | 30 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-24-3435dupG | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163120 | ||||||
chr13:46163154 | A | G | 1 | a0002c0002t0003g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-24-3468T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163154 | ||||||
chr13:46163165 | G | T | 131 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-24-3479C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163165 | ||||||
chr13:46163222 | G | A | 1 | a0001c0003t0004g0301 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-24-3536C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163222 | ||||||
chr13:46163403 | C | A | 18 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0196others(15): Show | 18 | HG01109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-24-3717G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163403 | ||||||
chr13:46163429 | T | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-24-3743A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163429 | ||||||
chr13:46163516 | T | A | 7 | a0001c0001t0001g0254a0001c0001t0002g0046a0001c0001t0002g0176others(4): Show | 7 | NA18954.hp1 NA18959.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24-3830A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163516 | ||||||
chr13:46163583 | T | C | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3897A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163583 | ||||||
chr13:46163584 | G | A | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3898C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163584 | ||||||
chr13:46163596 | A | G | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3910T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163596 | ||||||
chr13:46163608 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-3922G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163608 | ||||||
chr13:46163632 | T | TAAA | 7 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0196others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24-3947_-24-3946i others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163632 | ||||||
chr13:46163632 | TTA | T | 5 | a0001c0001t0003g0320a0001c0001t0006g0095a0001c0001t0006g0097others(2): Show | 5 | HG02145.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-3948_-24-3947d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163632 | ||||||
chr13:46163633 | T | A | 29 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0168others(26): Show | 30 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-24-3947A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163633 | ||||||
chr13:46163633 | T | TA | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(91): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-24-3948dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163633 | ||||||
chr13:46163633 | TA | T | 9 | a0001c0001t0001g0359a0001c0001t0002g0213a0001c0001t0002g0262others(6): Show | 10 | HG01934.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-3948delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163633 | ||||||
chr13:46163646 | A | AC | 5 | a0001c0001t0001g0254a0001c0001t0002g0046a0001c0001t0002g0176others(2): Show | 5 | NA18959.hp2 NA18978.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-3961_-24-3960i others(3): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163646 | ||||||
chr13:46163648 | A | C | 2 | a0001c0001t0006g0208a0001c0001t0007g0231 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-24-3962T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163648 | ||||||
chr13:46163653 | C | A | 9 | a0001c0001t0003g0216a0001c0001t0003g0307a0001c0001t0003g0320others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24-3967G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163653 | ||||||
chr13:46163671 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-24-3985T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163671 | ||||||
chr13:46163809 | T | C | 1 | a0001c0001t0028g0374 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-24-4123A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163809 | ||||||
chr13:46163889 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-24-4203C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163889 | ||||||
chr13:46163929 | A | G | 4 | a0001c0001t0002g0327a0001c0001t0002g0356a0001c0001t0002g0361others(1): Show | 4 | HG00639.hp1 HG02683.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-4243T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163929 | ||||||
chr13:46163942 | T | C | 3 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0003g0216 | 3 | HG02572.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-24-4256A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46163942 | ||||||
chr13:46164013 | T | C | 2 | a0001c0001t0001g0101a0001c0001t0002g0059 | 2 | HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-24-4327A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164013 | ||||||
chr13:46164126 | A | G | 1 | a0002c0002t0003g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-24-4440T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164126 | ||||||
chr13:46164396 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-24-4710G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164396 | ||||||
chr13:46164399 | G | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-24-4713C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164399 | ||||||
chr13:46164483 | G | A | 1 | a0001c0001t0026g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-24-4797C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164483 | ||||||
chr13:46164519 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-24-4833G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164519 | ||||||
chr13:46164610 | A | T | 4 | a0001c0001t0002g0336a0001c0001t0009g0303a0002c0002t0003g0310others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-4924T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164610 | ||||||
chr13:46164939 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-24-5253T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164939 | ||||||
chr13:46164947 | C | T | 67 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-24-5261G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46164947 | ||||||
chr13:46165153 | G | T | 1 | a0001c0001t0002g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-24-5467C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165153 | ||||||
chr13:46165306 | G | A | 1 | a0001c0001t0019g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-24-5620C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165306 | ||||||
chr13:46165361 | G | A | 6 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0177others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-5675C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165361 | ||||||
chr13:46165370 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-24-5684A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165370 | ||||||
chr13:46165490 | T | C | 16 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0196others(13): Show | 16 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24-5804A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165490 | ||||||
chr13:46165534 | A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(3): Show | 6 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-5848T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165534 | ||||||
chr13:46165644 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-5958C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165644 | ||||||
chr13:46165869 | A | T | 1 | a0001c0001t0020g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-24-6183T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165869 | ||||||
chr13:46165899 | G | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0003g0216 | 3 | HG02572.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-24-6213C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165899 | ||||||
chr13:46165920 | G | A | 6 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0177others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-6234C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165920 | ||||||
chr13:46165962 | GAAAA | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-6280_-24-6277d others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165962 | ||||||
chr13:46165963 | A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0185 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-24-6277T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165963 | ||||||
chr13:46165999 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-24-6313T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46165999 | ||||||
chr13:46166162 | A | T | 71 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-24-6476T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166162 | ||||||
chr13:46166334 | G | C | 1 | a0002c0002t0016g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-24-6648C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166334 | ||||||
chr13:46166386 | G | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-6700C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166386 | ||||||
chr13:46166676 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-24-6990C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166676 | ||||||
chr13:46166843 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-24-7157A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166843 | ||||||
chr13:46166897 | A | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7211T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166897 | ||||||
chr13:46166999 | T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7313A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46166999 | ||||||
chr13:46167368 | T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7682A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167368 | ||||||
chr13:46167373 | T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7687A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167373 | ||||||
chr13:46167427 | A | G | 96 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(93): Show | 98 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-24-7741T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167427 | ||||||
chr13:46167437 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7751C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167437 | ||||||
chr13:46167522 | T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7836A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167522 | ||||||
chr13:46167552 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-24-7866C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167552 | ||||||
chr13:46167683 | A | ATAT | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-8000_-24-7998d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167683 | ||||||
chr13:46167692 | G | T | 2 | a0001c0001t0006g0212a0001c0001t0013g0202 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24-8006C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167692 | ||||||
chr13:46167787 | C | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0003g0216 | 3 | HG02572.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-24-8101G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167787 | ||||||
chr13:46167885 | T | C | 2 | a0001c0001t0006g0208a0001c0001t0007g0231 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-24-8199A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46167885 | ||||||
chr13:46168154 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-24-8468T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168154 | ||||||
chr13:46168181 | T | A | 1 | a0001c0001t0001g0351 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-24-8495A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168181 | ||||||
chr13:46168196 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-24-8510T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168196 | ||||||
chr13:46168404 | G | A | 132 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-24-8718C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168404 | ||||||
chr13:46168415 | A | C | 1 | a0002c0002t0005g0129 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-24-8729T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168415 | ||||||
chr13:46168458 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-24-8772G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168458 | ||||||
chr13:46168543 | G | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0283a0001c0003t0004g0001 | 4 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-8857C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168543 | ||||||
chr13:46168556 | C | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0177others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-8870G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168556 | ||||||
chr13:46168632 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-24-8946G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168632 | ||||||
chr13:46168653 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-8967C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168653 | ||||||
chr13:46168661 | G | A | 1 | a0001c0001t0002g0345 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-24-8975C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168661 | ||||||
chr13:46168713 | A | G | 2 | a0001c0001t0008g0261a0001c0001t0008g0372 | 2 | NA18966.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24-9027T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168713 | ||||||
chr13:46168791 | C | T | 1 | a0002c0002t0005g0028 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-24-9105G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168791 | ||||||
chr13:46168792 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-24-9106C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46168792 | ||||||
chr13:46169043 | C | T | 2 | a0001c0001t0006g0212a0001c0001t0013g0202 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24-9357G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169043 | ||||||
chr13:46169059 | G | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-9373C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169059 | ||||||
chr13:46169061 | A | T | 1 | a0001c0001t0006g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-9375T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169061 | ||||||
chr13:46169072 | C | T | 1 | a0001c0001t0020g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-24-9386G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169072 | ||||||
chr13:46169111 | G | T | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-24-9425C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169111 | ||||||
chr13:46169256 | C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-9570G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169256 | ||||||
chr13:46169261 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-9575C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169261 | ||||||
chr13:46169363 | C | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0003g0216 | 3 | HG02572.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-24-9677G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169363 | ||||||
chr13:46169701 | C | T | 15 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0313others(12): Show | 15 | HG00639.hp2 HG01070.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24-10015G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169701 | ||||||
chr13:46169730 | G | A | 1 | a0001c0001t0002g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-24-10044C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169730 | ||||||
chr13:46169835 | A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-10149T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169835 | ||||||
chr13:46169947 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-10261C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46169947 | ||||||
chr13:46170010 | A | T | 132 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-24-10324T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170010 | ||||||
chr13:46170146 | A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-10460T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170146 | ||||||
chr13:46170149 | T | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0364 | 2 | NA18946.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-24-10463A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170149 | ||||||
chr13:46170164 | T | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0368a0001c0001t0002g0004others(10): Show | 14 | HG01496.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-24-10478A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170164 | ||||||
chr13:46170311 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-10625C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170311 | ||||||
chr13:46170317 | G | A | 71 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(68): Show | 72 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.-24-10631C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170317 | ||||||
chr13:46170502 | C | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-24-10816G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170502 | ||||||
chr13:46170580 | A | AT | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-10895dupA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170580 | ||||||
chr13:46170583 | T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-10897A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170583 | ||||||
chr13:46170644 | C | T | 2 | a0001c0001t0006g0208a0001c0001t0007g0231 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-24-10958G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170644 | ||||||
chr13:46170645 | G | A | 2 | a0001c0001t0003g0040a0001c0001t0009g0039 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-10959C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170645 | ||||||
chr13:46170742 | A | G | 1 | a0002c0002t0003g0198 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-24-11056T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170742 | ||||||
chr13:46170852 | G | A | 3 | a0001c0001t0001g0013a0001c0001t0002g0127a0001c0001t0002g0265 | 3 | HG03540.hp2 NA18971.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-24-11166C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46170852 | ||||||
chr13:46171396 | G | A | 111 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0025others(108): Show | 113 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-25+10715C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171396 | ||||||
chr13:46171503 | C | A | 8 | a0001c0001t0001g0368a0001c0001t0002g0082a0001c0001t0002g0325others(5): Show | 8 | HG01433.hp1 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+10608G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171503 | ||||||
chr13:46171533 | C | A | 3 | a0001c0001t0002g0111a0001c0001t0002g0323a0001c0001t0014g0275 | 3 | HG02056.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-25+10578G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171533 | ||||||
chr13:46171758 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-25+10353T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171758 | ||||||
chr13:46171784 | T | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-25+10327A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171784 | ||||||
chr13:46171800 | A | C | 117 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-25+10311T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171800 | ||||||
chr13:46171814 | T | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-25+10297A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171814 | ||||||
chr13:46171878 | T | A | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-25+10233A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171878 | ||||||
chr13:46171911 | T | C | 1 | a0001c0003t0004g0302 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-25+10200A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46171911 | ||||||
chr13:46172222 | G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG02683.hp2 HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-25+9889C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172222 | ||||||
chr13:46172407 | C | T | 8 | a0001c0001t0001g0368a0001c0001t0002g0082a0001c0001t0002g0325others(5): Show | 8 | HG01433.hp1 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+9704G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172407 | ||||||
chr13:46172415 | C | CA | 5 | a0001c0001t0002g0004a0001c0001t0002g0177a0001c0001t0002g0185others(2): Show | 6 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+9695dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172415 | ||||||
chr13:46172420 | G | C | 2 | a0001c0001t0008g0261a0001c0001t0008g0372 | 2 | NA18966.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-25+9691C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172420 | ||||||
chr13:46172484 | A | G | 3 | a0001c0003t0004g0002a0001c0003t0004g0160a0001c0003t0004g0224 | 4 | HG01257.hp1 HG01346.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+9627T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172484 | ||||||
chr13:46172526 | G | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(74): Show | 79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-25+9585C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172526 | ||||||
chr13:46172592 | G | A | 2 | a0001c0001t0006g0208a0001c0001t0007g0231 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-25+9519C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172592 | ||||||
chr13:46172766 | G | GGTTT | 133 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-25+9341_-25+9344d others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172766 | ||||||
chr13:46172886 | C | T | 1 | a0002c0002t0003g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-25+9225G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172886 | ||||||
chr13:46172994 | T | C | 116 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-25+9117A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46172994 | ||||||
chr13:46173049 | A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(143): Show | 148 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-25+9062T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173049 | ||||||
chr13:46173280 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-25+8831C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173280 | ||||||
chr13:46173332 | C | T | 2 | a0001c0003t0001g0084a0001c0003t0001g0340 | 2 | NA18974.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-25+8779G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173332 | ||||||
chr13:46173333 | G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0001g0134others(34): Show | 37 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.-25+8778C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173333 | ||||||
chr13:46173457 | G | A | 1 | a0002c0002t0005g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-25+8654C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173457 | ||||||
chr13:46173485 | A | G | 1 | a0001c0001t0002g0361 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-25+8626T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173485 | ||||||
chr13:46173592 | GT | G | 344 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(341): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-25+8518delA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173592 | ||||||
chr13:46173786 | G | A | 9 | a0001c0001t0001g0322a0001c0001t0001g0368a0001c0001t0002g0082others(6): Show | 9 | HG01433.hp1 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+8325C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173786 | ||||||
chr13:46173905 | A | C | 3 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0003g0216 | 3 | HG02572.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-25+8206T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173905 | ||||||
chr13:46173954 | T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0009g0222others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+8157A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46173954 | ||||||
chr13:46174074 | T | C | 97 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-25+8037A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174074 | ||||||
chr13:46174075 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-25+8036A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174075 | ||||||
chr13:46174098 | G | A | 1 | a0001c0001t0006g0144 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-25+8013C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174098 | ||||||
chr13:46174303 | C | A | 1 | a0001c0001t0009g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-25+7808G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174303 | ||||||
chr13:46174304 | A | AT | 98 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(95): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-25+7806dupA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174304 | ||||||
chr13:46174313 | A | T | 138 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0013others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-25+7798T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174313 | ||||||
chr13:46174314 | A | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0006g0212others(2): Show | 5 | HG01109.hp1 HG02717.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+7797T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174314 | ||||||
chr13:46174352 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-25+7759T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174352 | ||||||
chr13:46174353 | C | T | 104 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(101): Show | 106 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-25+7758G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174353 | ||||||
chr13:46174354 | G | A | 1 | a0001c0001t0023g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-25+7757C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174354 | ||||||
chr13:46174430 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-25+7681G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174430 | ||||||
chr13:46174453 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-25+7658G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174453 | ||||||
chr13:46174543 | T | C | 28 | a0001c0001t0001g0091a0001c0001t0001g0134a0001c0001t0001g0161others(25): Show | 28 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25+7568A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174543 | ||||||
chr13:46174566 | G | A | 8 | a0001c0001t0001g0368a0001c0001t0002g0082a0001c0001t0002g0325others(5): Show | 8 | HG01433.hp1 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+7545C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174566 | ||||||
chr13:46174629 | A | C | 22 | a0001c0001t0001g0091a0001c0001t0001g0117a0001c0001t0001g0134others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-25+7482T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174629 | ||||||
chr13:46174706 | C | T | 9 | a0001c0001t0001g0023a0001c0001t0001g0201a0001c0001t0003g0216others(6): Show | 9 | HG01070.hp2 HG01496.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+7405G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174706 | ||||||
chr13:46174778 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-25+7333C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174778 | ||||||
chr13:46174819 | C | T | 10 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0313others(7): Show | 10 | HG00639.hp2 HG01243.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+7292G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174819 | ||||||
chr13:46174834 | C | CA | 96 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(93): Show | 98 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-25+7276dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174834 | ||||||
chr13:46174834 | C | CAAA | 6 | a0001c0001t0001g0322a0001c0001t0002g0004a0001c0001t0002g0177others(3): Show | 7 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+7274_-25+7276d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174834 | ||||||
chr13:46174834 | CA | C | 11 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0146others(8): Show | 11 | HG01070.hp1 HG01256.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+7276delT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174834 | ||||||
chr13:46174834 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0001g0070a0001c0001t0001g0283a0001c0001t0018g0152others(1): Show | 5 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+7266_-25+7276d others(13): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174834 | ||||||
chr13:46174845 | A | G | 1 | a0001c0001t0002g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-25+7266T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174845 | ||||||
chr13:46174952 | T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(78): Show | 83 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-25+7159A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46174952 | ||||||
chr13:46175024 | A | G | 4 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0013g0016others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+7087T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175024 | ||||||
chr13:46175038 | A | G | 9 | a0001c0001t0001g0193a0001c0001t0001g0368a0001c0001t0002g0082others(6): Show | 9 | HG01192.hp2 HG01433.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+7073T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175038 | ||||||
chr13:46175106 | C | T | 40 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0033others(37): Show | 42 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-25+7005G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175106 | ||||||
chr13:46175119 | A | G | 16 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0001g0196others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+6992T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175119 | ||||||
chr13:46175179 | T | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-25+6932A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175179 | ||||||
chr13:46175244 | G | A | 7 | a0001c0001t0002g0010a0001c0001t0011g0246a0001c0001t0011g0247others(4): Show | 7 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+6867C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175244 | ||||||
chr13:46175271 | C | A | 35 | a0001c0001t0001g0036a0001c0001t0001g0115a0001c0001t0001g0128others(32): Show | 36 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-25+6840G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175271 | ||||||
chr13:46175508 | T | A | 1 | a0001c0001t0006g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25+6603A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175508 | ||||||
chr13:46175534 | G | A | 334 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(331): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-25+6577C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175534 | ||||||
chr13:46175582 | G | A | 45 | a0001c0001t0001g0013a0001c0001t0001g0178a0001c0001t0001g0183others(42): Show | 46 | HG01070.hp2 HG01074.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-25+6529C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175582 | ||||||
chr13:46175603 | C | T | 65 | a0001c0001t0001g0038a0001c0001t0001g0090a0001c0001t0001g0117others(62): Show | 66 | HG00140.hp1 HG00558.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.-25+6508G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175603 | ||||||
chr13:46175631 | T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0188a0001c0001t0003g0270others(3): Show | 6 | HG02145.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+6480A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175631 | ||||||
chr13:46175646 | T | C | 119 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(116): Show | 120 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-25+6465A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175646 | ||||||
chr13:46175666 | C | T | 10 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0205others(7): Show | 10 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+6445G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175666 | ||||||
chr13:46175689 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-25+6422G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175689 | ||||||
chr13:46175819 | G | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0364 | 2 | NA18946.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-25+6292C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175819 | ||||||
chr13:46175867 | A | G | 100 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0042others(97): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-25+6244T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175867 | ||||||
chr13:46175945 | T | C | 137 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0021others(134): Show | 139 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-25+6166A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175945 | ||||||
chr13:46175980 | A | T | 17 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0205others(14): Show | 17 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-25+6131T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46175980 | ||||||
chr13:46176096 | T | C | 4 | a0001c0001t0001g0132a0001c0001t0002g0371a0001c0001t0004g0373others(1): Show | 4 | NA18966.hp2 NA19007.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+6015A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176096 | ||||||
chr13:46176200 | G | A | 20 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0183others(17): Show | 21 | HG01243.hp2 HG01891.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.-25+5911C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176200 | ||||||
chr13:46176260 | C | T | 195 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(192): Show | 196 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.-25+5851G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176260 | ||||||
chr13:46176356 | G | GA | 52 | a0001c0001t0001g0013a0001c0001t0001g0146a0001c0001t0001g0148others(49): Show | 54 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-25+5754dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176356 | ||||||
chr13:46176395 | A | T | 63 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0146others(60): Show | 65 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.-25+5716T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176395 | ||||||
chr13:46176416 | G | T | 7 | a0001c0001t0001g0145a0001c0001t0011g0246a0001c0001t0011g0247others(4): Show | 7 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+5695C>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176416 | ||||||
chr13:46176497 | A | T | 1 | a0005c0012t0002g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-25+5614T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176497 | ||||||
chr13:46176649 | G | GT | 11 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(8): Show | 11 | HG00323.hp1 HG00733.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+5461dupA | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176649 | ||||||
chr13:46176676 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-25+5435G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176676 | ||||||
chr13:46176688 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-25+5423T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176688 | ||||||
chr13:46176709 | A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18953.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-25+5402T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176709 | ||||||
chr13:46176746 | T | C | 6 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0327others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+5365A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176746 | ||||||
chr13:46176808 | A | C | 1 | a0001c0001t0011g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-25+5303T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176808 | ||||||
chr13:46176865 | G | A | 1 | a0002c0002t0003g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-25+5246C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176865 | ||||||
chr13:46176869 | G | A | 1 | a0002c0002t0003g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-25+5242C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176869 | ||||||
chr13:46176875 | T | G | 1 | a0002c0002t0003g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-25+5236A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176875 | ||||||
chr13:46176875 | T | TTG | 22 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0188others(19): Show | 23 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25+5234_-25+5235d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176875 | ||||||
chr13:46176875 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0011g0246a0001c0001t0011g0247a0002c0002t0003g0245others(3): Show | 6 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+5228_-25+5235d others(10): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176875 | ||||||
chr13:46176875 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-25+5222_-25+5235d others(16): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176875 | ||||||
chr13:46176875 | TTG | T | 113 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0037others(110): Show | 114 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-25+5234_-25+5235d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176875 | ||||||
chr13:46176900 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-25+5211A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176900 | ||||||
chr13:46176900 | T | C | 7 | a0001c0001t0001g0171a0001c0001t0002g0149a0001c0001t0002g0174others(4): Show | 8 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+5211A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176900 | ||||||
chr13:46176902 | T | A | 124 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(121): Show | 125 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-25+5209A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176902 | ||||||
chr13:46176902 | T | TGA | 85 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(82): Show | 85 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-25+5207_-25+5208d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176902 | ||||||
chr13:46176902 | T | TGTGA | 12 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(9): Show | 12 | HG01123.hp2 HG02040.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25+5208_-25+5209i others(6): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176902 | ||||||
chr13:46176904 | A | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0269others(7): Show | 10 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+5207T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176904 | ||||||
chr13:46176911 | G | A | 2 | a0001c0001t0002g0192a0002c0002t0016g0191 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-25+5200C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46176911 | ||||||
chr13:46177162 | C | T | 2 | a0001c0001t0001g0274a0001c0001t0014g0275 | 2 | HG01123.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-25+4949G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177162 | ||||||
chr13:46177188 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-25+4923T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177188 | ||||||
chr13:46177367 | C | T | 27 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0139others(24): Show | 27 | HG00558.hp1 HG01496.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+4744G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177367 | ||||||
chr13:46177460 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-25+4651A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177460 | ||||||
chr13:46177501 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-25+4610C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177501 | ||||||
chr13:46177512 | C | A | 27 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0139others(24): Show | 27 | HG00558.hp1 HG01496.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+4599G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177512 | ||||||
chr13:46177554 | C | G | 1 | a0001c0001t0001g0367 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-25+4557G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177554 | ||||||
chr13:46177557 | T | G | 1 | a0001c0001t0001g0367 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-25+4554A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177557 | ||||||
chr13:46177628 | G | A | 1 | a0005c0012t0002g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-25+4483C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177628 | ||||||
chr13:46177648 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-25+4463C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177648 | ||||||
chr13:46177686 | G | A | 6 | a0001c0001t0011g0246a0001c0001t0011g0247a0002c0002t0003g0245others(3): Show | 6 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+4425C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177686 | ||||||
chr13:46177778 | T | C | 2 | a0001c0001t0023g0194a0005c0012t0002g0195 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-25+4333A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177778 | ||||||
chr13:46177851 | T | TTGC | 9 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0003g0270others(6): Show | 9 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+4257_-25+4259d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177851 | ||||||
chr13:46177854 | C | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0037others(89): Show | 93 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25+4257G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177854 | ||||||
chr13:46177864 | T | A | 1 | a0001c0001t0022g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25+4247A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177864 | ||||||
chr13:46177883 | AATG | A | 8 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0205others(5): Show | 8 | HG02886.hp2 HG02922.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+4225_-25+4227d others(5): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177883 | ||||||
chr13:46177924 | T | TA | 249 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(246): Show | 251 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(248): Show |
intron_variant | MODIFIER | c.-25+4186dupT | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177924 | ||||||
chr13:46177928 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-25+4183T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46177928 | ||||||
chr13:46178027 | C | CATGTTTA others(11): Show |
20 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0188others(17): Show | 21 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-25+4083_-25+4084i others(20): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178027 | ||||||
chr13:46178028 | T | A | 20 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0188others(17): Show | 21 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-25+4083A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178028 | ||||||
chr13:46178226 | A | G | 1 | a0001c0001t0023g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-25+3885T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178226 | ||||||
chr13:46178234 | A | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0003g0270others(6): Show | 9 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+3877T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178234 | ||||||
chr13:46178235 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-25+3876G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178235 | ||||||
chr13:46178271 | C | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0023others(16): Show | 19 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-25+3840G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178271 | ||||||
chr13:46178380 | T | A | 1 | a0001c0001t0002g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-25+3731A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178380 | ||||||
chr13:46178381 | A | T | 1 | a0001c0001t0002g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-25+3730T>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178381 | ||||||
chr13:46178453 | C | G | 1 | a0001c0001t0013g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-25+3658G>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178453 | ||||||
chr13:46178496 | C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0002g0147 | 3 | HG01256.hp2 HG01943.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-25+3615G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178496 | ||||||
chr13:46178536 | C | A | 190 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(187): Show | 191 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.-25+3575G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178536 | ||||||
chr13:46178563 | G | A | 190 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(187): Show | 191 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.-25+3548C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178563 | ||||||
chr13:46178569 | G | A | 246 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(243): Show | 248 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(245): Show |
intron_variant | MODIFIER | c.-25+3542C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178569 | ||||||
chr13:46178653 | C | T | 1 | a0001c0003t0001g0340 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-25+3458G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178653 | ||||||
chr13:46178678 | G | A | 199 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(196): Show | 200 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.-25+3433C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178678 | ||||||
chr13:46178734 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-25+3377C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178734 | ||||||
chr13:46178739 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-25+3372T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178739 | ||||||
chr13:46178892 | T | G | 6 | a0001c0001t0011g0246a0001c0001t0011g0247a0002c0002t0003g0245others(3): Show | 6 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+3219A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178892 | ||||||
chr13:46178987 | A | G | 28 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0139others(25): Show | 28 | HG00558.hp1 HG01496.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25+3124T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46178987 | ||||||
chr13:46179067 | T | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0136a0001c0001t0001g0137others(34): Show | 37 | HG00558.hp1 HG01070.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-25+3044A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179067 | ||||||
chr13:46179072 | T | C | 2 | a0001c0001t0023g0194a0005c0012t0002g0195 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-25+3039A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179072 | ||||||
chr13:46179102 | T | C | 1 | a0001c0001t0006g0144 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-25+3009A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179102 | ||||||
chr13:46179251 | A | G | 6 | a0001c0001t0011g0246a0001c0001t0011g0247a0002c0002t0003g0245others(3): Show | 6 | HG01070.hp2 HG01496.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+2860T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179251 | ||||||
chr13:46179360 | G | A | 15 | a0001c0001t0001g0196a0001c0001t0001g0199a0001c0001t0001g0201others(12): Show | 16 | HG01975.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+2751C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179360 | ||||||
chr13:46179382 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-25+2729T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179382 | ||||||
chr13:46179407 | A | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0257others(25): Show | 28 | HG01070.hp2 HG01109.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.-25+2704T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179407 | ||||||
chr13:46179437 | A | G | 197 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0021others(194): Show | 198 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.-25+2674T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179437 | ||||||
chr13:46179866 | A | G | 1 | a0001c0001t0006g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-25+2245T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179866 | ||||||
chr13:46179970 | T | TTC | 27 | a0001c0001t0001g0254a0001c0001t0001g0257a0001c0001t0001g0264others(24): Show | 27 | HG01070.hp2 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.-25+2139_-25+2140d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179970 | ||||||
chr13:46179998 | GCT | G | 7 | a0001c0001t0001g0207a0001c0001t0001g0334a0001c0001t0006g0206others(4): Show | 8 | HG00099.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+2111_-25+2112d others(4): Show |
LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46179998 | ||||||
chr13:46180017 | C | T | 2 | a0001c0001t0001g0013a0002c0002t0003g0014 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-25+2094G>A | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180017 | ||||||
chr13:46180060 | T | A | 27 | a0001c0001t0001g0254a0001c0001t0001g0257a0001c0001t0001g0264others(24): Show | 27 | HG01070.hp2 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.-25+2051A>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180060 | ||||||
chr13:46180181 | T | G | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-25+1930A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180181 | ||||||
chr13:46180284 | T | C | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG02080.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.-25+1827A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180284 | ||||||
chr13:46180486 | A | G | 3 | a0001c0001t0002g0337a0001c0001t0010g0338a0001c0001t0010g0339 | 3 | HG00140.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-25+1625T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180486 | ||||||
chr13:46180599 | T | C | 28 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0001g0220others(25): Show | 28 | HG00099.hp1 HG01257.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-25+1512A>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180599 | ||||||
chr13:46180637 | G | C | 3 | a0001c0001t0007g0240a0002c0002t0003g0241a0002c0002t0003g0242 | 3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-25+1474C>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180637 | ||||||
chr13:46180814 | A | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-25+1297T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46180814 | ||||||
chr13:46181251 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-25+860C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181251 | ||||||
chr13:46181298 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-25+813T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181298 | ||||||
chr13:46181417 | A | G | 1 | a0001c0001t0002g0336 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25+694T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181417 | ||||||
chr13:46181567 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-25+544A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181567 | ||||||
chr13:46181639 | A | C | 2 | a0001c0001t0001g0009a0001c0001t0002g0010 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-25+472T>G | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181639 | ||||||
chr13:46181716 | C | A | 27 | a0001c0001t0001g0254a0001c0001t0001g0257a0001c0001t0001g0264others(24): Show | 27 | HG01070.hp2 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.-25+395G>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181716 | ||||||
chr13:46181717 | A | G | 306 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0015others(303): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.-25+394T>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181717 | ||||||
chr13:46181745 | T | G | 32 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0348others(29): Show | 32 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-25+366A>C | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181745 | ||||||
chr13:46181886 | G | A | 1 | a0001c0001t0001g0368 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-25+225C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46181886 | ||||||
chr13:46182054 | G | A | 5 | a0001c0001t0001g0369a0001c0001t0002g0371a0001c0001t0004g0373others(2): Show | 5 | HG02040.hp1 NA18966.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+57C>T | LCP1 | ENSG00000136167.15 | transcript | ENST00000323076.7 | protein_coding | 1/15 | chr13 | 46182054 |