geneid | 348801 |
---|---|
ensemblid | ENSG00000206535.8 |
hgncid | 28014 |
symbol | LNP1 |
name | leukemia NUP98 fusion partner 1 |
refseq_nuc | NM_001085451.2 |
refseq_prot | NP_001078920.1 |
ensembl_nuc | ENST00000383693.8 |
ensembl_prot | ENSP00000373191.3 |
mane_status | MANE Select |
chr | chr3 |
start | 100401539 |
end | 100456319 |
strand | + |
ver | v1.2 |
region | chr3:100401539-100456319 |
region5000 | chr3:100396539-100461319 |
regionname0 | LNP1_chr3_100401539_100456319 |
regionname5000 | LNP1_chr3_100396539_100461319 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 197 | 207 | 45 | 24 | 113 | 6 | 18 | 91 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002 | 1/0 | 178 | 191 | 45 | 48 | 67 | 6 | 24 | 49 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 594 | 206 | 44 | 24 | 113 | 6 | 18 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
c0002 | 1/0 | 537 | 190 | 44 | 48 | 67 | 6 | 24 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
c0003 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
c0004 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1328 | 232 | 60 | 35 | 120 | 1 | 16 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0002 | 0/1 | 1328 | 68 | 0 | 13 | 36 | 6 | 12 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0003 | 1/0 | 1328 | 67 | 7 | 22 | 18 | 5 | 14 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0004 | 0/0 | 1328 | 12 | 11 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0005 | 0/0 | 1328 | 7 | 7 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0006 | 0/0 | 1328 | 5 | 0 | 0 | 5 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0007 | 0/0 | 1328 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0008 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0009 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0010 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0011 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0012 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
t0013 | 0/0 | 1328 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0016 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 594 | 206 | 44 | 24 | 113 | 6 | 18 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0004 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002 | 1/0 | 537 | 190 | 44 | 48 | 67 | 6 | 24 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0003 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1921 | 128 | 37 | 13 | 73 | 0 | 5 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0001t0002 | 0/1 | 1921 | 63 | 0 | 9 | 36 | 6 | 11 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0001t0003 | 0/0 | 1921 | 3 | 0 | 1 | 0 | 0 | 2 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0001t0005 | 0/0 | 1921 | 7 | 7 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0001t0006 | 0/0 | 1921 | 4 | 0 | 0 | 4 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0001t0007 | 0/0 | 1921 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0001c0004t0004 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0001 | 0/0 | 1864 | 104 | 23 | 22 | 47 | 1 | 11 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0002 | 0/0 | 1864 | 5 | 0 | 4 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0003 | 1/0 | 1864 | 64 | 7 | 21 | 18 | 5 | 12 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0004 | 0/0 | 1864 | 11 | 10 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0006 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0008 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0009 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0011 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0012 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0002t0013 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
a0002c0003t0010 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | copy fasta | chr3 | 100396539 | 100461319 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0016 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0006g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0001t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0001c0004t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0003g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0002t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
a0002c0003t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0318 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0344 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00140 | hp1 | a0002 | c0002 | t0003 | g0084 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0308 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0092 | EUR | FIN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0178 | EUR | FIN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00639 | hp1 | a0002 | c0002 | t0003 | g0097 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0364 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01070 | hp2 | a0002 | c0002 | t0003 | g0113 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0118 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0307 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01081 | hp1 | a0002 | c0002 | t0003 | g0129 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01099 | hp1 | a0002 | c0002 | t0004 | g0149 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01099 | hp2 | a0002 | c0002 | t0003 | g0107 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01167 | hp1 | a0002 | c0002 | t0003 | g0114 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01169 | hp2 | a0002 | c0002 | t0003 | g0119 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0146 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01192 | hp1 | a0002 | c0002 | t0003 | g0091 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01255 | hp2 | a0002 | c0002 | t0003 | g0093 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0117 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0313 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0374 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0311 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01516 | hp1 | a0002 | c0002 | t0003 | g0128 | EUR | IBS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0336 | EUR | IBS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0090 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01934 | hp1 | a0002 | c0002 | t0003 | g0127 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01934 | hp2 | a0002 | c0002 | t0003 | g0094 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0373 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01943 | hp2 | a0002 | c0002 | t0003 | g0130 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0096 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01978 | hp1 | a0002 | c0002 | t0003 | g0126 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0347 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01993 | hp2 | a0002 | c0002 | t0003 | g0122 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0284 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0078 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0342 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02155 | hp2 | a0002 | c0002 | t0003 | g0131 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0139 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0145 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0124 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0150 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02615 | hp1 | a0001 | c0004 | t0004 | g0203 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02615 | hp2 | a0002 | c0002 | t0008 | g0165 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0116 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0112 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02717 | hp2 | a0002 | c0002 | t0004 | g0192 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0104 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02738 | hp2 | a0002 | c0002 | t0003 | g0102 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0120 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0164 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02970 | hp2 | a0002 | c0002 | t0003 | g0098 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0276 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03041 | hp1 | a0002 | c0002 | t0004 | g0077 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03130 | hp1 | a0002 | c0002 | t0004 | g0176 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03195 | hp2 | a0002 | c0002 | t0009 | g0045 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03225 | hp2 | a0002 | c0002 | t0004 | g0076 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0108 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0274 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03486 | hp2 | a0002 | c0003 | t0010 | g0205 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0132 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0348 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0137 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03579 | hp1 | a0002 | c0002 | t0012 | g0305 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0134 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0089 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0105 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0349 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0265 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0371 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0177 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0179 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0331 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0095 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0136 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0243 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18943 | hp1 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18960 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18962 | hp2 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18964 | hp1 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18969 | hp1 | a0002 | c0002 | t0003 | g0141 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18973 | hp1 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18977 | hp2 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18990 | hp1 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18998 | hp2 | a0002 | c0002 | t0013 | g0100 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19030 | hp2 | a0002 | c0002 | t0004 | g0193 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19043 | hp2 | a0002 | c0002 | t0011 | g0148 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19057 | hp2 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19067 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19077 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19078 | hp2 | a0002 | c0002 | t0006 | g0234 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19086 | hp1 | a0002 | c0002 | t0003 | g0101 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0025 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0147 | AFR | ASW | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | ASW | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0334 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0088 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20805 | hp1 | a0002 | c0002 | t0003 | g0142 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0319 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0356 | SAS | GIH | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20905 | hp2 | a0002 | c0002 | t0003 | g0083 | SAS | GIH | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01123 | hp1 | a0002 | c0002 | t0003 | g0135 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG03471 | hp2 | a0002 | c0002 | t0004 | g0079 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0103 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18955 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0016 | REF | REF | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0003 | g0115 | REF | REF | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100451756
|
A | ATCCTAGA others(50): Show |
1 | a0001 | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
disruptive_inframe_insertion | MODERATE | c.221_222insGGAATTCC others(49): Show |
p.Gln74_Glu75insGluP others(53): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/4 | 1156/1864 | 222/537 | 74/178 | INFO_REALIGN_3_PRIME | chr3 | 100451756 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100455788
|
C | T | 1 | a0002c0003 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.399C>T | p.Ser133Ser | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 1333/1864 | 399/537 | 133/178 | chr3 | 100455788 | ||
chr3:100455878
|
G | A | 1 | a0001c0001 | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
synonymous_variant | LOW | c.489G>A | p.Glu163Glu | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 1423/1864 | 489/537 | 163/178 | chr3 | 100455878 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100401637
|
C | T | 2 | a0001c0001t0006a0002c0002t0006 | 5 | HG00673.hp2 NA18955.hp1 NA18978.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-836C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 28093 | chr3 | 100401637 | |||||
chr3:100401879
|
G | A | 2 | a0001c0001t0007a0002c0002t0008 | 2 | HG01074.hp2 HG02615.hp2 |
5_prime_UTR_variant | MODIFIER | c.-594G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27851 | chr3 | 100401879 | |||||
chr3:100402006
|
G | A | 14 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
5_prime_UTR_variant | MODIFIER | c.-467G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27724 | chr3 | 100402006 | |||||
chr3:100402073
|
A | G | 1 | a0002c0002t0013 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-400A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27657 | chr3 | 100402073 | |||||
chr3:100402103
|
A | G | 1 | a0001c0001t0005 | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-370A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | chr3 | 100402103 | ||||||
chr3:100402182
|
G | A | 1 | a0002c0002t0009 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-291G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27548 | chr3 | 100402182 | |||||
chr3:100402277
|
G | A | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
5_prime_UTR_variant | MODIFIER | c.-196G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27453 | chr3 | 100402277 | |||||
chr3:100402296
|
T | C | 3 | a0001c0001t0002a0001c0001t0007a0002c0002t0002 | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(66): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-177T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | chr3 | 100402296 | ||||||
chr3:100402352
|
T | C | 1 | a0002c0003t0010 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27378 | chr3 | 100402352 | |||||
chr3:100456042
|
A | G | 3 | a0001c0004t0004a0002c0002t0004a0002c0002t0008 | 13 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*116A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 116 | chr3 | 100456042 | |||||
chr3:100456115
|
C | G | 1 | a0002c0002t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 189 | chr3 | 100456115 | |||||
chr3:100456206
|
A | G | 1 | a0001c0001t0005 | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*280A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 280 | chr3 | 100456206 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100402479
|
T | A | 1 | a0002c0002t0001g0019 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-34+40T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402479 | ||||||
chr3:100402643
|
AT | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(63): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.-34+217delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100402643 | |||||
chr3:100402786
|
A | C | 1 | a0001c0001t0002g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+347A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402786 | ||||||
chr3:100402789
|
C | A | 1 | a0001c0001t0002g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+350C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402789 | ||||||
chr3:100402792
|
T | A | 1 | a0001c0001t0002g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+353T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402792 | ||||||
chr3:100402793
|
T | A | 1 | a0001c0001t0002g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+354T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402793 | ||||||
chr3:100403061
|
A | G | 1 | a0002c0002t0003g0374 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-34+622A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403061 | ||||||
chr3:100403066
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-34+627C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403066 | ||||||
chr3:100403165
|
C | T | 1 | a0001c0001t0001g0372 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-34+726C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403165 | ||||||
chr3:100403220
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | NA18990.hp2 NA19058.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-34+781T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403220 | ||||||
chr3:100403237
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(305): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.-34+798C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403237 | ||||||
chr3:100403324
|
G | A | 1 | a0002c0002t0011g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34+885G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403324 | ||||||
chr3:100403412
|
T | C | 1 | a0002c0002t0003g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-34+973T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403412 | ||||||
chr3:100403995
|
T | A | 2 | a0002c0002t0004g0149a0002c0002t0004g0150 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-34+1556T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403995 | ||||||
chr3:100404016
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+1577T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404016 | ||||||
chr3:100404106
|
C | T | 1 | a0001c0001t0002g0371 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-34+1667C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404106 | ||||||
chr3:100404489
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-34+2050T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404489 | ||||||
chr3:100404501
|
C | T | 5 | a0001c0001t0001g0075a0002c0002t0004g0076a0002c0002t0004g0077others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+2062C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404501 | ||||||
chr3:100404630
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 250 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.-34+2191G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404630 | ||||||
chr3:100404747
|
A | G | 1 | a0002c0002t0001g0301 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-34+2308A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404747 | ||||||
chr3:100404751
|
C | T | 1 | a0002c0002t0003g0147 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-34+2312C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404751 | ||||||
chr3:100404790
|
C | CG | 6 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(3): Show | 6 | HG02559.hp1 HG02897.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+2351_-34+2352i others(3): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404790 | ||||||
chr3:100404791
|
C | CT | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 132 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-34+2369dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100404791 | |||||
chr3:100404791
|
C | CTT | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(54): Show | 64 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-34+2368_-34+2369d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100404791 | |||||
chr3:100404791
|
C | CTTT | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0072others(55): Show | 60 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-34+2367_-34+2369d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100404791 | |||||
chr3:100404791
|
C | T | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+2352C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404791 | ||||||
chr3:100404896
|
G | A | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-34+2457G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404896 | ||||||
chr3:100405029
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-34+2590T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405029 | ||||||
chr3:100405249
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+2810A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405249 | ||||||
chr3:100405268
|
A | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(107): Show | 119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+2829A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405268 | ||||||
chr3:100405289
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-34+2850C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405289 | ||||||
chr3:100405329
|
T | C | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+2890T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405329 | ||||||
chr3:100405451
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-34+3012C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405451 | ||||||
chr3:100405534
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 250 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.-34+3095A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405534 | ||||||
chr3:100405654
|
A | G | 1 | a0001c0001t0002g0362 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-34+3215A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405654 | ||||||
chr3:100405692
|
C | G | 1 | a0002c0002t0001g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34+3253C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405692 | ||||||
chr3:100405724
|
C | T | 4 | a0001c0001t0002g0358a0001c0001t0002g0359a0001c0001t0002g0360others(1): Show | 4 | HG00438.hp2 HG02074.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+3285C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405724 | ||||||
chr3:100405803
|
T | A | 1 | a0002c0002t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-34+3364T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405803 | ||||||
chr3:100405870
|
A | G | 2 | a0001c0001t0003g0143a0001c0001t0003g0144 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-34+3431A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405870 | ||||||
chr3:100406065
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 10 | HG00597.hp1 HG02027.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+3626C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406065 | ||||||
chr3:100406201
|
G | A | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+3762G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406201 | ||||||
chr3:100406217
|
C | T | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+3778C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406217 | ||||||
chr3:100406243
|
C | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0024 | 3 | HG02132.hp2 NA18747.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-34+3804C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406243 | ||||||
chr3:100406463
|
G | T | 1 | a0001c0001t0002g0357 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34+4024G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406463 | ||||||
chr3:100406484
|
A | C | 1 | a0002c0002t0001g0293 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-34+4045A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406484 | ||||||
chr3:100406607
|
T | A | 6 | a0001c0001t0001g0075a0002c0002t0004g0025a0002c0002t0004g0076others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+4168T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406607 | ||||||
chr3:100406637
|
C | T | 1 | a0002c0002t0003g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-34+4198C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406637 | ||||||
chr3:100406650
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 5 | HG02109.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+4211T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406650 | ||||||
chr3:100406657
|
C | T | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+4218C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406657 | ||||||
chr3:100406679
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG02015.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-34+4240T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406679 | ||||||
chr3:100406855
|
A | G | 1 | a0002c0002t0001g0292 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-34+4416A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406855 | ||||||
chr3:100406934
|
C | T | 1 | a0001c0001t0002g0356 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-34+4495C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406934 | ||||||
chr3:100406982
|
T | A | 2 | a0002c0002t0001g0206a0002c0002t0001g0248 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-34+4543T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406982 | ||||||
chr3:100407171
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 8 | NA18945.hp1 NA18965.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+4732G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407171 | ||||||
chr3:100407369
|
G | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18988.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-34+4930G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407369 | ||||||
chr3:100407405
|
A | G | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+4966A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407405 | ||||||
chr3:100407435
|
A | T | 1 | a0002c0002t0001g0291 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-34+4996A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407435 | ||||||
chr3:100407448
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 5 | HG02109.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+5009A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407448 | ||||||
chr3:100407477
|
G | A | 39 | a0001c0001t0001g0373a0002c0002t0001g0019a0002c0002t0001g0160others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34+5038G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407477 | ||||||
chr3:100407672
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-34+5233A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407672 | ||||||
chr3:100407715
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-34+5276G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407715 | ||||||
chr3:100408143
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-34+5704C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408143 | ||||||
chr3:100408239
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34+5800A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408239 | ||||||
chr3:100408397
|
C | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(107): Show | 119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+5958C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408397 | ||||||
chr3:100408417
|
G | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(107): Show | 119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+5978G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408417 | ||||||
chr3:100408521
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-34+6082G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408521 | ||||||
chr3:100408575
|
A | T | 38 | a0001c0001t0001g0373a0002c0002t0001g0019a0002c0002t0001g0160others(35): Show | 38 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-34+6136A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408575 | ||||||
chr3:100408675
|
A | C | 2 | a0002c0002t0004g0149a0002c0002t0004g0150 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-34+6236A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408675 | ||||||
chr3:100408696
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0366a0001c0001t0001g0367others(6): Show | 10 | HG01099.hp1 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+6257C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408696 | ||||||
chr3:100408796
|
C | T | 1 | a0002c0002t0003g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-34+6357C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408796 | ||||||
chr3:100408797
|
G | A | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-34+6358G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408797 | ||||||
chr3:100408833
|
G | A | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+6394G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408833 | ||||||
chr3:100408993
|
G | A | 2 | a0002c0002t0003g0083a0002c0002t0003g0084 | 2 | HG00140.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-34+6554G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408993 | ||||||
chr3:100409104
|
T | C | 1 | a0001c0001t0002g0304 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-34+6665T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409104 | ||||||
chr3:100409129
|
G | A | 3 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0087 | 3 | NA18947.hp1 NA18962.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-34+6690G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409129 | ||||||
chr3:100409169
|
G | A | 2 | a0001c0001t0001g0031a0002c0002t0001g0032 | 2 | NA19063.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-34+6730G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409169 | ||||||
chr3:100409538
|
C | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+7099C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409538 | ||||||
chr3:100409540
|
C | A | 11 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0005g0074others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34+7101C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409540 | ||||||
chr3:100409542
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 229 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.-34+7103C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409542 | ||||||
chr3:100409544
|
A | C | 6 | a0001c0001t0002g0350a0001c0001t0002g0351a0001c0001t0002g0352others(3): Show | 6 | NA18951.hp2 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7105A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409544 | ||||||
chr3:100409553
|
TAC | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+7116_-34+7117d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409553 | |||||
chr3:100409553
|
TACATACA others(5): Show |
T | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+7118_-34+7129d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409553 | |||||
chr3:100409557
|
T | TAC | 11 | a0001c0001t0003g0143a0002c0002t0003g0089a0002c0002t0003g0090others(8): Show | 11 | HG00639.hp1 HG01175.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34+7152_-34+7153d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | |||||
chr3:100409557
|
TAC | T | 34 | a0001c0001t0002g0308a0001c0001t0007g0307a0001c0004t0004g0203others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-34+7152_-34+7153d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | |||||
chr3:100409557
|
TACAC | T | 7 | a0001c0001t0002g0304a0001c0001t0002g0309a0001c0001t0002g0310others(4): Show | 7 | HG02602.hp2 HG02717.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+7150_-34+7153d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | |||||
chr3:100409557
|
TACACAC | T | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+7148_-34+7153d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | |||||
chr3:100409559
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-34+7120C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409559 | ||||||
chr3:100409561
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+7122C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409561 | ||||||
chr3:100409563
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-34+7124C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409563 | ||||||
chr3:100409567
|
C | T | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+7128C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409567 | ||||||
chr3:100409571
|
C | T | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+7132C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409571 | ||||||
chr3:100409576
|
A | G | 1 | a0001c0001t0002g0361 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-34+7137A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409576 | ||||||
chr3:100409587
|
CACACAT | C | 6 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0001g0197others(3): Show | 6 | HG01099.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7150_-34+7155d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409587 | |||||
chr3:100409589
|
C | T | 62 | a0001c0001t0001g0202a0001c0001t0001g0230a0001c0001t0001g0231others(59): Show | 64 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.-34+7150C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409589 | ||||||
chr3:100409589
|
CACAT | C | 3 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0368 | 3 | HG02896.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-34+7152_-34+7155d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409589 | |||||
chr3:100409591
|
C | T | 161 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(158): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-34+7152C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409591 | ||||||
chr3:100409591
|
CAT | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0370a0002c0002t0003g0138 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+7167_-34+7168d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409591 | |||||
chr3:100409593
|
T | C | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(22): Show | 27 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-34+7154T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409593 | ||||||
chr3:100409595
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-34+7156T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409595 | ||||||
chr3:100409601
|
TATA | T | 5 | a0001c0001t0002g0348a0001c0001t0002g0357a0001c0001t0002g0360others(2): Show | 5 | HG00738.hp2 HG01981.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+7163_-34+7165d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409601 | ||||||
chr3:100409602
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34+7163A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409602 | ||||||
chr3:100409603
|
TATA | T | 53 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0302others(50): Show | 55 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.-34+7165_-34+7167d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409603 | ||||||
chr3:100409604
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(38): Show | 48 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-34+7165A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409604 | ||||||
chr3:100409605
|
TA | T | 6 | a0001c0001t0002g0306a0001c0001t0002g0358a0002c0002t0001g0158others(3): Show | 6 | HG00438.hp2 HG00735.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7167delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409605 | ||||||
chr3:100409606
|
A | ATATATTT | 5 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 6 | HG02109.hp2 HG02630.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+7168_-34+7169i others(9): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409606 | |||||
chr3:100409606
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0033others(14): Show | 19 | HG01106.hp1 HG01952.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-34+7167A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409606 | ||||||
chr3:100409606
|
A | T | 14 | a0001c0001t0002g0348a0001c0001t0002g0357a0001c0001t0002g0360others(11): Show | 14 | HG00323.hp1 HG00738.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+7167A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409606 | ||||||
chr3:100409606
|
AT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 152 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-34+7181delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409606 | |||||
chr3:100409606
|
ATTT | A | 11 | a0001c0001t0001g0063a0001c0001t0001g0226a0001c0001t0001g0230others(8): Show | 11 | HG02257.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+7179_-34+7181d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409606 | |||||
chr3:100409607
|
T | TA | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(26): Show | 33 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.-34+7168_-34+7169i others(3): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409607 | ||||||
chr3:100409608
|
T | A | 48 | a0001c0001t0001g0202a0001c0001t0001g0366a0001c0001t0001g0367others(45): Show | 48 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-34+7169T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409608 | ||||||
chr3:100409609
|
T | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 169 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-34+7170T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409609 | ||||||
chr3:100409610
|
T | A | 4 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0168others(1): Show | 4 | HG00544.hp2 HG01496.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+7171T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409610 | ||||||
chr3:100409611
|
T | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+7172T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409611 | ||||||
chr3:100409613
|
T | A | 6 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+7174T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409613 | ||||||
chr3:100409751
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-34+7312T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409751 | ||||||
chr3:100409844
|
C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 60 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-34+7405C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409844 | ||||||
chr3:100409865
|
G | A | 20 | a0001c0001t0001g0250a0001c0001t0001g0261a0002c0002t0001g0242others(17): Show | 20 | HG00423.hp1 HG00642.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34+7426G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409865 | ||||||
chr3:100409883
|
C | A | 1 | a0001c0001t0003g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34+7444C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409883 | ||||||
chr3:100409956
|
C | CATCT | 78 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0063others(75): Show | 79 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-34+7559_-34+7562d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | |||||
chr3:100409956
|
C | CATCTATC others(1): Show |
3 | a0001c0001t0002g0344a0002c0002t0001g0191a0002c0002t0003g0136 | 3 | HG00099.hp2 HG04228.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-34+7555_-34+7562d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | |||||
chr3:100409956
|
C | CATCTATC others(5): Show |
3 | a0002c0002t0001g0206a0002c0002t0001g0248a0002c0002t0003g0137 | 3 | HG02258.hp2 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-34+7551_-34+7562d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | |||||
chr3:100409956
|
C | CATCTATC others(9): Show |
3 | a0001c0001t0001g0272a0001c0001t0002g0345a0001c0001t0002g0346 | 3 | HG01346.hp1 NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-34+7547_-34+7562d others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | |||||
chr3:100409956
|
CATCT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0026others(27): Show | 33 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-34+7559_-34+7562d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | |||||
chr3:100409956
|
CATCTATC others(1): Show |
C | 9 | a0001c0001t0001g0005a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 11 | HG00597.hp1 HG01361.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+7555_-34+7562d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | |||||
chr3:100410046
|
C | G | 1 | a0002c0002t0011g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34+7607C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410046 | ||||||
chr3:100410155
|
G | A | 20 | a0001c0001t0001g0250a0001c0001t0001g0261a0002c0002t0001g0242others(17): Show | 20 | HG00423.hp1 HG00642.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34+7716G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410155 | ||||||
chr3:100410282
|
T | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(58): Show | 70 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34+7843T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410282 | ||||||
chr3:100410365
|
TAAA | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(114): Show | 127 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-34+7927_-34+7929d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410365 | ||||||
chr3:100410524
|
T | C | 59 | a0001c0001t0002g0017a0001c0001t0002g0302a0001c0001t0002g0303others(56): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-34+8085T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410524 | ||||||
chr3:100410654
|
G | A | 1 | a0002c0002t0001g0286 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34+8215G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410654 | ||||||
chr3:100410866
|
C | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 71 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-34+8427C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410866 | ||||||
chr3:100410887
|
A | G | 1 | a0002c0002t0001g0190 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-34+8448A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410887 | ||||||
chr3:100411039
|
C | A | 1 | a0002c0002t0012g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34+8600C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411039 | ||||||
chr3:100411072
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+8633C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411072 | ||||||
chr3:100411109
|
A | T | 3 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0001g0197 | 3 | HG02809.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-34+8670A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411109 | ||||||
chr3:100411169
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-34+8730A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411169 | ||||||
chr3:100411426
|
G | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(107): Show | 119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+8987G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411426 | ||||||
chr3:100411604
|
G | A | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+9165G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411604 | ||||||
chr3:100411779
|
C | T | 1 | a0002c0002t0001g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-34+9340C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411779 | ||||||
chr3:100411865
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-34+9426A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411865 | ||||||
chr3:100411888
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-34+9449G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411888 | ||||||
chr3:100412001
|
G | C | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG00741.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-34+9562G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412001 | ||||||
chr3:100412002
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+9563A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412002 | ||||||
chr3:100412030
|
A | G | 1 | a0001c0001t0002g0357 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34+9591A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412030 | ||||||
chr3:100412044
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-34+9605G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412044 | ||||||
chr3:100412294
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-34+9855G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412294 | ||||||
chr3:100412394
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(110): Show | 123 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-34+9955C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412394 | ||||||
chr3:100412401
|
T | G | 1 | a0001c0001t0002g0353 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-34+9962T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412401 | ||||||
chr3:100412935
|
C | T | 2 | a0001c0001t0002g0365a0002c0002t0002g0349 | 2 | HG03831.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-34+10496C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412935 | ||||||
chr3:100413053
|
A | G | 67 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0302others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.-34+10614A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413053 | ||||||
chr3:100413076
|
C | T | 25 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0072others(22): Show | 27 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34+10637C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413076 | ||||||
chr3:100413077
|
G | A | 2 | a0001c0001t0001g0198a0002c0003t0010g0205 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34+10638G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413077 | ||||||
chr3:100413110
|
C | A | 1 | a0002c0002t0004g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+10671C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413110 | ||||||
chr3:100413132
|
C | G | 67 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0302others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.-34+10693C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413132 | ||||||
chr3:100413254
|
G | A | 4 | a0002c0002t0004g0076a0002c0002t0004g0077a0002c0002t0004g0078others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+10815G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413254 | ||||||
chr3:100413720
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+11281T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413720 | ||||||
chr3:100413830
|
A | G | 1 | a0002c0002t0003g0135 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-34+11391A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413830 | ||||||
chr3:100413845
|
G | A | 1 | a0002c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-34+11406G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413845 | ||||||
chr3:100413873
|
A | T | 8 | a0002c0002t0003g0088a0002c0002t0003g0090a0002c0002t0003g0091others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+11434A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413873 | ||||||
chr3:100414053
|
G | C | 39 | a0001c0001t0001g0373a0002c0002t0001g0019a0002c0002t0001g0160others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34+11614G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414053 | ||||||
chr3:100414161
|
C | T | 3 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0330 | 3 | HG01981.hp1 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-34+11722C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414161 | ||||||
chr3:100414449
|
A | G | 2 | a0001c0001t0001g0198a0002c0003t0010g0205 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34+12010A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414449 | ||||||
chr3:100414462
|
G | A | 2 | a0002c0002t0001g0167a0002c0002t0001g0168 | 2 | HG00544.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-34+12023G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414462 | ||||||
chr3:100414465
|
T | G | 1 | a0002c0002t0003g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-34+12026T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414465 | ||||||
chr3:100414546
|
TA | T | 8 | a0001c0001t0001g0031a0002c0002t0001g0188a0002c0002t0001g0189others(5): Show | 8 | HG00639.hp2 HG01081.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+12122delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100414546 | |||||
chr3:100414792
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 52 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34+12353G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414792 | ||||||
chr3:100414899
|
C | T | 4 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0368others(1): Show | 4 | HG02896.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+12460C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414899 | ||||||
chr3:100415009
|
G | A | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34+12570G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415009 | ||||||
chr3:100415133
|
G | T | 34 | a0001c0001t0001g0373a0002c0002t0001g0019a0002c0002t0001g0160others(31): Show | 34 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-34+12694G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415133 | ||||||
chr3:100415356
|
T | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+12917T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415356 | ||||||
chr3:100415391
|
A | G | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+12952A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415391 | ||||||
chr3:100415499
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-34+13060A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415499 | ||||||
chr3:100415675
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-34+13236C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415675 | ||||||
chr3:100415758
|
A | G | 9 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0368others(6): Show | 9 | HG01099.hp1 HG02280.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+13319A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415758 | ||||||
chr3:100415829
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-34+13390C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415829 | ||||||
chr3:100415943
|
C | T | 2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | NA18980.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-34+13504C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415943 | ||||||
chr3:100416101
|
A | G | 2 | a0001c0001t0001g0366a0001c0001t0001g0368 | 2 | HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-33-13596A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416101 | ||||||
chr3:100416114
|
A | T | 2 | a0001c0001t0001g0198a0002c0003t0010g0205 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-33-13583A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416114 | ||||||
chr3:100416158
|
G | A | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-13539G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416158 | ||||||
chr3:100416181
|
AT | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0153 | 4 | HG02109.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-13514delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416181 | |||||
chr3:100416406
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-33-13291C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416406 | ||||||
chr3:100416467
|
T | C | 2 | a0001c0001t0002g0315a0001c0001t0002g0335 | 2 | HG04228.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-33-13230T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416467 | ||||||
chr3:100416594
|
CTT | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0056others(67): Show | 74 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416594 | |||||
chr3:100416597
|
T | G | 1 | a0001c0001t0002g0336 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-33-13100T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416597 | ||||||
chr3:100416597
|
T | TG | 5 | a0001c0001t0001g0280a0002c0002t0001g0166a0002c0002t0001g0167others(2): Show | 5 | HG00544.hp2 HG00738.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33-13100_-33-1309 others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416597 | ||||||
chr3:100416597
|
T | TTG | 31 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0073others(28): Show | 33 | HG00609.hp2 HG00673.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33-13099_-33-1309 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
T | TTGTG | 11 | a0001c0001t0001g0266a0001c0001t0001g0285a0001c0001t0002g0017others(8): Show | 12 | HG00735.hp2 HG01496.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.-33-13099_-33-1309 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
T | TTGTGTGT others(3): Show |
1 | a0002c0002t0001g0191 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33-13099_-33-1309 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
TTTTG | T | 38 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0211others(35): Show | 41 | HG00099.hp1 HG00099.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
TTTTGTG | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0026others(42): Show | 51 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
TTTTGTGT others(1): Show |
T | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(21): Show | 26 | HG00423.hp2 HG01106.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
TTTTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-13098_-33-1308 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
TTTTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-33-13098_-33-1308 others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416597
|
TTTTGTGT others(9): Show |
T | 1 | a0001c0001t0002g0316 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-33-13098_-33-1308 others(20): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | |||||
chr3:100416599
|
T | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(128): Show | 138 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-33-13098T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416599 | ||||||
chr3:100416599
|
T | TTG | 4 | a0001c0001t0003g0143a0002c0002t0003g0127a0002c0002t0003g0130others(1): Show | 4 | HG01934.hp1 HG01943.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-13051_-33-1305 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | |||||
chr3:100416599
|
T | TTGTG | 3 | a0001c0001t0003g0144a0002c0002t0003g0083a0002c0002t0003g0095 | 3 | HG04115.hp1 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-33-13053_-33-1305 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | |||||
chr3:100416599
|
T | TTTTTTGT others(3): Show |
1 | a0001c0001t0003g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-33-13097_-33-1309 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | |||||
chr3:100416599
|
TTG | T | 6 | a0002c0002t0003g0092a0002c0002t0003g0094a0002c0002t0003g0098others(3): Show | 6 | HG00323.hp1 HG01361.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-13051_-33-1305 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | |||||
chr3:100416599
|
TTGTG | T | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0087others(13): Show | 16 | HG01099.hp2 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-33-13053_-33-1305 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | |||||
chr3:100416599
|
TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-33-13063_-33-1305 others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | |||||
chr3:100416601
|
G | T | 3 | a0002c0002t0003g0128a0002c0002t0003g0133a0002c0002t0003g0134 | 3 | HG01516.hp1 HG03654.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-33-13096G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416601 | ||||||
chr3:100416603
|
G | T | 1 | a0002c0002t0003g0374 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-33-13094G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416603 | ||||||
chr3:100416605
|
G | T | 1 | a0002c0002t0003g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-33-13092G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416605 | ||||||
chr3:100416718
|
AT | A | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(117): Show | 129 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-33-12964delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416718 | |||||
chr3:100416718
|
ATT | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 72 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-33-12965_-33-1296 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416718 | |||||
chr3:100416732
|
TTA | T | 38 | a0001c0001t0001g0373a0002c0002t0001g0019a0002c0002t0001g0160others(35): Show | 38 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-33-12964_-33-1296 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416732 | ||||||
chr3:100416734
|
A | G | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-12963A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416734 | ||||||
chr3:100416780
|
T | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(183): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-33-12917T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416780 | ||||||
chr3:100416849
|
C | T | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-12848C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416849 | ||||||
chr3:100416887
|
C | T | 14 | a0001c0001t0001g0373a0002c0002t0001g0019a0002c0002t0001g0166others(11): Show | 14 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33-12810C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416887 | ||||||
chr3:100417020
|
T | G | 3 | a0001c0001t0005g0295a0001c0001t0005g0296a0001c0001t0005g0298 | 3 | HG02559.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-33-12677T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417020 | ||||||
chr3:100417128
|
A | G | 1 | a0002c0002t0001g0284 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-33-12569A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417128 | ||||||
chr3:100417158
|
CA | C | 3 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0001g0197 | 3 | HG02809.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-33-12534delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417158 | |||||
chr3:100417316
|
C | T | 2 | a0001c0001t0001g0198a0002c0003t0010g0205 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-33-12381C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417316 | ||||||
chr3:100417371
|
C | CT | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 280 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.-33-12304dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | |||||
chr3:100417371
|
C | CTT | 13 | a0001c0001t0001g0029a0001c0001t0001g0237a0001c0001t0001g0269others(10): Show | 13 | HG01099.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-33-12305_-33-1230 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | |||||
chr3:100417371
|
CT | C | 6 | a0001c0001t0002g0332a0001c0001t0002g0351a0001c0001t0002g0363others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-12304delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | |||||
chr3:100417371
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0006g0234 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-33-12313_-33-1230 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | |||||
chr3:100417525
|
G | A | 1 | a0002c0002t0001g0249 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-33-12172G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417525 | ||||||
chr3:100417800
|
A | G | 66 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0302others(63): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-33-11897A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417800 | ||||||
chr3:100417844
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-33-11853C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417844 | ||||||
chr3:100418007
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-33-11690A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418007 | ||||||
chr3:100418059
|
A | AC | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 68 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-33-11638_-33-1163 others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418059 | ||||||
chr3:100418060
|
T | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(244): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-33-11637T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418060 | ||||||
chr3:100418220
|
C | A | 1 | a0002c0002t0001g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33-11477C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418220 | ||||||
chr3:100418220
|
C | T | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-11477C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418220 | ||||||
chr3:100418226
|
AT | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-11456delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100418226 | |||||
chr3:100418355
|
G | A | 1 | a0001c0001t0007g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-33-11342G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418355 | ||||||
chr3:100418529
|
C | G | 1 | a0002c0002t0001g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33-11168C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418529 | ||||||
chr3:100418848
|
A | G | 2 | a0001c0001t0002g0321a0001c0001t0002g0325 | 2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-33-10849A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418848 | ||||||
chr3:100418876
|
G | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0063 | 3 | HG02257.hp1 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-33-10821G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418876 | ||||||
chr3:100418941
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 71 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-33-10756A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418941 | ||||||
chr3:100419412
|
A | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-33-10285A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419412 | ||||||
chr3:100419559
|
C | T | 2 | a0002c0002t0001g0003a0002c0002t0001g0054 | 4 | NA18961.hp2 NA18966.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-10138C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419559 | ||||||
chr3:100419839
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33-9858G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419839 | ||||||
chr3:100419851
|
G | C | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-9846G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419851 | ||||||
chr3:100420300
|
G | T | 1 | a0001c0001t0002g0330 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-33-9397G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420300 | ||||||
chr3:100420371
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-9326G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420371 | ||||||
chr3:100420860
|
C | T | 1 | a0002c0002t0001g0052 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-33-8837C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420860 | ||||||
chr3:100420873
|
C | G | 1 | a0001c0001t0002g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-33-8824C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420873 | ||||||
chr3:100421035
|
G | A | 1 | a0002c0002t0012g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33-8662G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421035 | ||||||
chr3:100421036
|
T | G | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-8661T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421036 | ||||||
chr3:100421047
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-8650C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421047 | ||||||
chr3:100421148
|
A | T | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-8549A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421148 | ||||||
chr3:100421196
|
T | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-8501T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421196 | ||||||
chr3:100421569
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(4): Show | 9 | NA18945.hp1 NA18954.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-8128G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421569 | ||||||
chr3:100421716
|
G | T | 1 | a0001c0001t0001g0236 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-33-7981G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421716 | ||||||
chr3:100422182
|
CT | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.-33-7496delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422182 | |||||
chr3:100422182
|
CTT | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0366a0001c0001t0001g0367others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-7497_-33-7496d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422182 | |||||
chr3:100422486
|
G | A | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-7211G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100422486 | ||||||
chr3:100422803
|
C | CT | 14 | a0001c0001t0002g0304a0001c0001t0002g0312a0001c0001t0002g0316others(11): Show | 14 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33-6867dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422803
|
CT | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(125): Show | 138 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-33-6867delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422803
|
CTT | C | 19 | a0001c0001t0001g0034a0001c0001t0001g0208a0001c0001t0001g0214others(16): Show | 19 | HG01069.hp1 HG01167.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-33-6868_-33-6867d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422803
|
CTTT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 64 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-33-6869_-33-6867d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422803
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-6876_-33-6867d others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422803
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0366 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33-6877_-33-6867d others(13): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422803
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0367a0001c0001t0001g0368a0002c0002t0004g0149others(3): Show | 6 | HG01099.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-6878_-33-6867d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | |||||
chr3:100422827
|
T | A | 2 | a0001c0001t0005g0074a0001c0001t0005g0300 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-33-6870T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100422827 | ||||||
chr3:100422870
|
A | C | 66 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0302others(63): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-33-6827A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100422870 | ||||||
chr3:100423120
|
T | C | 1 | a0001c0001t0002g0335 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-33-6577T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423120 | ||||||
chr3:100423241
|
T | C | 1 | a0001c0001t0006g0232 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-33-6456T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423241 | ||||||
chr3:100423315
|
A | G | 1 | a0001c0001t0002g0362 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-33-6382A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423315 | ||||||
chr3:100423436
|
T | C | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-6261T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423436 | ||||||
chr3:100423455
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0153 | 4 | HG02109.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-6242C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423455 | ||||||
chr3:100423477
|
G | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(111): Show | 124 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-33-6220G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423477 | ||||||
chr3:100423612
|
G | A | 1 | a0002c0002t0013g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-33-6085G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423612 | ||||||
chr3:100423704
|
A | C | 1 | a0002c0002t0001g0168 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-33-5993A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423704 | ||||||
chr3:100423739
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0073others(11): Show | 16 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-33-5958A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423739 | ||||||
chr3:100423843
|
C | T | 1 | a0002c0002t0003g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-33-5854C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423843 | ||||||
chr3:100423977
|
C | T | 1 | a0001c0001t0002g0327 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-33-5720C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423977 | ||||||
chr3:100424153
|
C | T | 1 | a0002c0002t0011g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33-5544C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424153 | ||||||
chr3:100424175
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-33-5522G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424175 | ||||||
chr3:100424280
|
G | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-5417G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424280 | ||||||
chr3:100424461
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-33-5236A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424461 | ||||||
chr3:100424464
|
C | A | 7 | a0002c0002t0001g0163a0002c0002t0001g0182a0002c0002t0001g0183others(4): Show | 7 | NA18953.hp1 NA18974.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-5233C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424464 | ||||||
chr3:100424526
|
A | G | 1 | a0002c0002t0012g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33-5171A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424526 | ||||||
chr3:100424617
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-5080G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424617 | ||||||
chr3:100424627
|
A | G | 1 | a0002c0002t0003g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-33-5070A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424627 | ||||||
chr3:100424712
|
G | A | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-4985G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424712 | ||||||
chr3:100424743
|
C | T | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-4954C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424743 | ||||||
chr3:100425143
|
A | G | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-4554A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425143 | ||||||
chr3:100425180
|
A | G | 2 | a0001c0001t0002g0321a0001c0001t0002g0325 | 2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-33-4517A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425180 | ||||||
chr3:100425215
|
C | T | 22 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(19): Show | 27 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-4482C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425215 | ||||||
chr3:100425240
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0002g0375 | 2 | HG02572.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-33-4457C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425240 | ||||||
chr3:100425271
|
C | A | 2 | a0002c0002t0001g0064a0002c0002t0009g0045 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-33-4426C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425271 | ||||||
chr3:100425342
|
T | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-4355T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425342 | ||||||
chr3:100425537
|
T | C | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-4160T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425537 | ||||||
chr3:100425562
|
G | A | 1 | a0002c0002t0004g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-33-4135G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425562 | ||||||
chr3:100425567
|
T | C | 2 | a0001c0001t0001g0202a0001c0004t0004g0203 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-4130T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425567 | ||||||
chr3:100425569
|
T | A | 1 | a0002c0002t0001g0286 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-33-4128T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425569 | ||||||
chr3:100425578
|
C | G | 2 | a0002c0002t0001g0158a0002c0002t0001g0245 | 2 | HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-33-4119C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425578 | ||||||
chr3:100425686
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0004t0004g0203others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-4011G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425686 | ||||||
chr3:100425846
|
A | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(116): Show | 129 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-33-3851A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425846 | ||||||
chr3:100425909
|
C | G | 1 | a0002c0002t0004g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-33-3788C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425909 | ||||||
chr3:100425982
|
C | A | 1 | a0001c0001t0002g0302 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-33-3715C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425982 | ||||||
chr3:100426581
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-33-3116G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426581 | ||||||
chr3:100426667
|
G | A | 1 | a0002c0002t0001g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-33-3030G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426667 | ||||||
chr3:100426725
|
A | C | 10 | a0001c0001t0001g0228a0002c0002t0001g0206a0002c0002t0001g0248others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33-2972A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426725 | ||||||
chr3:100426955
|
T | G | 2 | a0002c0002t0004g0149a0002c0002t0004g0150 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-33-2742T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426955 | ||||||
chr3:100427025
|
T | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(21): Show | 27 | HG01069.hp2 HG01243.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-2672T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427025 | ||||||
chr3:100427081
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(17): Show | 22 | HG01952.hp2 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-33-2616T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427081 | ||||||
chr3:100427704
|
C | T | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-1993C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427704 | ||||||
chr3:100427726
|
A | G | 1 | a0002c0002t0004g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-33-1971A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427726 | ||||||
chr3:100427765
|
G | A | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1932G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427765 | ||||||
chr3:100428063
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-33-1634A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428063 | ||||||
chr3:100428132
|
G | A | 4 | a0001c0001t0002g0308a0001c0001t0002g0337a0001c0001t0002g0338others(1): Show | 4 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-1565G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428132 | ||||||
chr3:100428168
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-33-1529A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428168 | ||||||
chr3:100428267
|
C | T | 10 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(7): Show | 10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33-1430C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428267 | ||||||
chr3:100428348
|
A | G | 1 | a0002c0002t0003g0112 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-33-1349A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428348 | ||||||
chr3:100428409
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-33-1288G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428409 | ||||||
chr3:100428459
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-33-1238G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428459 | ||||||
chr3:100428462
|
G | C | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-1235G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428462 | ||||||
chr3:100428467
|
G | T | 6 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(3): Show | 6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-1230G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428467 | ||||||
chr3:100428531
|
C | CAA | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-33-1154_-33-1153d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100428531 | |||||
chr3:100428548
|
A | G | 1 | a0001c0001t0005g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-33-1149A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428548 | ||||||
chr3:100428795
|
C | T | 1 | a0002c0002t0001g0040 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-33-902C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428795 | ||||||
chr3:100428961
|
A | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-736A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428961 | ||||||
chr3:100428986
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-33-711G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428986 | ||||||
chr3:100429079
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-33-618T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429079 | ||||||
chr3:100429140
|
C | G | 1 | a0001c0001t0002g0357 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-33-557C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429140 | ||||||
chr3:100429283
|
G | A | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-33-414G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429283 | ||||||
chr3:100429315
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-33-382G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429315 | ||||||
chr3:100429329
|
T | A | 1 | a0001c0001t0001g0226 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-33-368T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429329 | ||||||
chr3:100429427
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-33-270G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429427 | ||||||
chr3:100429513
|
A | G | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-184A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429513 | ||||||
chr3:100429541
|
C | G | 1 | a0002c0002t0003g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-33-156C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429541 | ||||||
chr3:100429907
|
G | A | 1 | a0002c0002t0003g0112 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.156+22G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100429907 | ||||||
chr3:100429960
|
A | G | 1 | a0001c0001t0002g0328 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.156+75A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100429960 | ||||||
chr3:100429991
|
A | C | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG00741.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.156+106A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100429991 | ||||||
chr3:100430170
|
C | T | 2 | a0002c0002t0001g0263a0002c0002t0001g0265 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.156+285C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430170 | ||||||
chr3:100430189
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.156+304A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430189 | ||||||
chr3:100430221
|
C | A | 3 | a0001c0001t0003g0099a0001c0001t0003g0143a0001c0001t0003g0144 | 3 | HG01074.hp1 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+336C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430221 | ||||||
chr3:100430310
|
G | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(62): Show | 72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.156+425G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430310 | ||||||
chr3:100430434
|
A | G | 6 | a0002c0002t0001g0163a0002c0002t0001g0182a0002c0002t0001g0183others(3): Show | 6 | NA18953.hp1 NA18974.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+549A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430434 | ||||||
chr3:100430698
|
G | A | 1 | a0002c0002t0002g0364 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.156+813G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430698 | ||||||
chr3:100430891
|
C | G | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+1006C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430891 | ||||||
chr3:100431183
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+1298A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431183 | ||||||
chr3:100431198
|
T | G | 2 | a0001c0001t0003g0143a0001c0001t0003g0144 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+1313T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431198 | ||||||
chr3:100431643
|
A | G | 1 | a0001c0001t0005g0299 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.156+1758A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431643 | ||||||
chr3:100431694
|
C | A | 1 | a0002c0002t0001g0286 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.156+1809C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431694 | ||||||
chr3:100431821
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(6): Show | 10 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+1936C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431821 | ||||||
chr3:100431828
|
C | CA | 30 | a0001c0001t0001g0028a0001c0001t0001g0198a0001c0001t0001g0202others(27): Show | 30 | HG00423.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.156+1963dupA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431828 | |||||
chr3:100431828
|
CA | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0033others(24): Show | 28 | HG01070.hp2 HG01123.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.156+1963delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431828 | |||||
chr3:100431828
|
CAA | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(40): Show | 49 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.156+1962_156+1963d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431828 | |||||
chr3:100431948
|
A | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2063A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431948 | ||||||
chr3:100431990
|
GTTTATA | G | 3 | a0002c0002t0003g0094a0002c0002t0003g0127a0002c0002t0003g0140 | 3 | HG01934.hp1 HG01934.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.156+2107_156+2112d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(3): Show |
G | 1 | a0002c0002t0003g0141 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.156+2107_156+2116d others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(11): Show |
G | 1 | a0002c0002t0001g0035 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.156+2107_156+2124d others(20): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(15): Show |
G | 1 | a0001c0001t0001g0281 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.156+2107_156+2128d others(24): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(17): Show |
G | 3 | a0001c0001t0001g0272a0001c0001t0001g0366a0001c0001t0001g0368 | 3 | HG01346.hp1 HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.156+2107_156+2130d others(26): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(19): Show |
G | 16 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 19 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.156+2107_156+2132d others(28): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(21): Show |
G | 11 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 12 | HG01074.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+2107_156+2134d others(30): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(23): Show |
G | 23 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(20): Show | 25 | HG00597.hp2 HG00642.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.156+2107_156+2136d others(32): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(25): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.156+2107_156+2138d others(34): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(27): Show |
G | 6 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0002g0325others(3): Show | 6 | HG00438.hp2 HG00741.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+2107_156+2140d others(36): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431990
|
GTTTATAT others(29): Show |
G | 62 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0034others(59): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.156+2107_156+2142d others(38): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | |||||
chr3:100431991
|
TTTATATA others(6): Show |
T | 1 | a0002c0002t0003g0135 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.156+2108_156+2120d others(15): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431991 | |||||
chr3:100431992
|
TTA | T | 12 | a0002c0002t0001g0170a0002c0002t0001g0177a0002c0002t0001g0265others(9): Show | 13 | HG00738.hp1 HG01358.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.156+2167_156+2168d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATA | T | 9 | a0002c0002t0001g0243a0002c0002t0001g0284a0002c0002t0003g0087others(6): Show | 9 | HG01099.hp1 HG02004.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+2165_156+2168d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATA | T | 14 | a0002c0002t0001g0194a0002c0002t0001g0196a0002c0002t0001g0251others(11): Show | 14 | HG00735.hp2 HG01258.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.156+2163_156+2168d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(1): Show |
T | 30 | a0002c0002t0001g0041a0002c0002t0001g0158a0002c0002t0001g0167others(27): Show | 30 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.156+2161_156+2168d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(3): Show |
T | 34 | a0001c0001t0001g0051a0001c0001t0001g0198a0002c0002t0001g0002others(31): Show | 36 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.156+2159_156+2168d others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(5): Show |
T | 17 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0052others(14): Show | 17 | HG00323.hp1 HG00639.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.156+2157_156+2168d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(7): Show |
T | 10 | a0002c0002t0001g0044a0002c0002t0001g0048a0002c0002t0001g0049others(7): Show | 10 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+2155_156+2168d others(16): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(9): Show |
T | 21 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0022others(18): Show | 24 | HG00741.hp1 HG01169.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.156+2153_156+2168d others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(11): Show |
T | 4 | a0002c0002t0001g0169a0002c0002t0001g0180a0002c0002t0001g0185others(1): Show | 4 | HG01070.hp1 HG01168.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+2151_156+2168d others(20): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(13): Show |
T | 8 | a0002c0002t0001g0019a0002c0002t0001g0064a0002c0002t0001g0166others(5): Show | 8 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.156+2149_156+2168d others(22): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(15): Show |
T | 2 | a0002c0002t0001g0062a0002c0002t0003g0106 | 2 | NA18945.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.156+2147_156+2168d others(24): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(19): Show |
T | 1 | a0002c0002t0004g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.156+2143_156+2168d others(28): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(21): Show |
T | 1 | a0002c0002t0003g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.156+2141_156+2168d others(30): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(23): Show |
T | 1 | a0002c0002t0001g0024 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.156+2139_156+2168d others(32): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(25): Show |
T | 4 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0262others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+2137_156+2168d others(34): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(27): Show |
T | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.156+2135_156+2168d others(36): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(29): Show |
T | 1 | a0002c0002t0001g0286 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.156+2133_156+2168d others(38): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(35): Show |
T | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2127_156+2168d others(44): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100431992
|
TTATATAT others(41): Show |
T | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+2121_156+2168d others(50): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | |||||
chr3:100432000
|
ATATATAT others(32): Show |
A | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+2116_156+2154d others(41): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432000 | ||||||
chr3:100432140
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2255C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432140 | ||||||
chr3:100432141
|
CT | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2258delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100432141 | |||||
chr3:100432255
|
T | A | 1 | a0002c0002t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.156+2370T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432255 | ||||||
chr3:100432285
|
CT | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+2407delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100432285 | |||||
chr3:100432311
|
G | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.156+2426G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432311 | ||||||
chr3:100432322
|
T | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2437T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432322 | ||||||
chr3:100432600
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156+2715T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432600 | ||||||
chr3:100432643
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2758A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432643 | ||||||
chr3:100432666
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2781A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432666 | ||||||
chr3:100432669
|
A | G | 6 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(3): Show | 6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+2784A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432669 | ||||||
chr3:100433096
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.156+3211C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433096 | ||||||
chr3:100433114
|
G | A | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+3229G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433114 | ||||||
chr3:100433178
|
C | A | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+3293C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433178 | ||||||
chr3:100433250
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+3365G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433250 | ||||||
chr3:100433263
|
C | T | 1 | a0002c0002t0003g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.156+3378C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433263 | ||||||
chr3:100433353
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(6): Show | 11 | HG01952.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+3468G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433353 | ||||||
chr3:100433396
|
T | A | 1 | a0001c0001t0002g0340 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.156+3511T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433396 | ||||||
chr3:100433493
|
T | C | 4 | a0001c0001t0002g0308a0001c0001t0002g0337a0001c0001t0002g0338others(1): Show | 4 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+3608T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433493 | ||||||
chr3:100433587
|
G | A | 22 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(19): Show | 27 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.156+3702G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433587 | ||||||
chr3:100433641
|
A | G | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+3756A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433641 | ||||||
chr3:100433730
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+3845G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433730 | ||||||
chr3:100433767
|
G | A | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+3882G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433767 | ||||||
chr3:100433778
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156+3893T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433778 | ||||||
chr3:100433827
|
C | T | 1 | a0002c0002t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.156+3942C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433827 | ||||||
chr3:100433933
|
T | C | 1 | a0002c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.156+4048T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433933 | ||||||
chr3:100433962
|
T | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(57): Show | 68 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.156+4077T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433962 | ||||||
chr3:100433986
|
T | C | 1 | a0001c0001t0002g0321 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.156+4101T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433986 | ||||||
chr3:100434014
|
T | C | 2 | a0002c0002t0001g0242a0002c0002t0002g0364 | 2 | HG00735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.156+4129T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434014 | ||||||
chr3:100434022
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.156+4137T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434022 | ||||||
chr3:100434142
|
C | T | 1 | a0002c0002t0003g0133 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.156+4257C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434142 | ||||||
chr3:100434226
|
C | T | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(58): Show | 69 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.156+4341C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434226 | ||||||
chr3:100434428
|
T | C | 1 | a0001c0001t0002g0340 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.156+4543T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434428 | ||||||
chr3:100434477
|
C | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+4592C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434477 | ||||||
chr3:100434673
|
C | T | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+4788C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434673 | ||||||
chr3:100434780
|
C | T | 2 | a0002c0002t0001g0274a0002c0002t0001g0276 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.156+4895C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434780 | ||||||
chr3:100434785
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0153 | 3 | HG02109.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.156+4900T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434785 | ||||||
chr3:100434825
|
G | A | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+4940G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434825 | ||||||
chr3:100434831
|
CT | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.156+4963delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100434831 | |||||
chr3:100434848
|
T | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 62 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.156+4963T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434848 | ||||||
chr3:100434912
|
A | G | 2 | a0002c0002t0004g0149a0002c0002t0004g0150 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.156+5027A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434912 | ||||||
chr3:100435022
|
C | T | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156+5137C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435022 | ||||||
chr3:100435024
|
C | G | 1 | a0002c0002t0012g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.156+5139C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435024 | ||||||
chr3:100435078
|
TTGTATTT others(4): Show |
T | 1 | a0001c0001t0002g0355 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.156+5207_156+5217d others(13): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100435078 | |||||
chr3:100435231
|
C | G | 69 | a0002c0002t0001g0032a0002c0002t0001g0041a0002c0002t0001g0042others(66): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.156+5346C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435231 | ||||||
chr3:100435273
|
T | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(338): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.156+5388T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435273 | ||||||
chr3:100435317
|
G | T | 58 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(55): Show | 63 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.156+5432G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435317 | ||||||
chr3:100435336
|
A | C | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+5451A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435336 | ||||||
chr3:100435555
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+5670A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435555 | ||||||
chr3:100435640
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0030 | 2 | NA18965.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.156+5755G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435640 | ||||||
chr3:100435677
|
G | A | 12 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(9): Show | 12 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+5792G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435677 | ||||||
chr3:100435861
|
A | G | 1 | a0002c0002t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.156+5976A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435861 | ||||||
chr3:100435960
|
G | T | 1 | a0002c0002t0001g0293 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.156+6075G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435960 | ||||||
chr3:100436072
|
T | C | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.156+6187T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436072 | ||||||
chr3:100436194
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+6309G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436194 | ||||||
chr3:100436329
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+6444T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436329 | ||||||
chr3:100436338
|
C | A | 1 | a0002c0002t0003g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.156+6453C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436338 | ||||||
chr3:100436396
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.156+6511G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436396 | ||||||
chr3:100436445
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0002g0359a0001c0001t0002g0360 | 3 | NA18950.hp2 NA18983.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.156+6560C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436445 | ||||||
chr3:100436446
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0229 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.156+6561G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436446 | ||||||
chr3:100436569
|
T | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+6684T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436569 | ||||||
chr3:100436682
|
T | C | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156+6797T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436682 | ||||||
chr3:100436703
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+6818A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436703 | ||||||
chr3:100436810
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+6925T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436810 | ||||||
chr3:100436853
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+6968G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436853 | ||||||
chr3:100436904
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.156+7019C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436904 | ||||||
chr3:100436923
|
T | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+7038T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436923 | ||||||
chr3:100436924
|
A | T | 1 | a0001c0001t0001g0225 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.156+7039A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436924 | ||||||
chr3:100436943
|
G | A | 2 | a0002c0002t0002g0311a0002c0002t0002g0347 | 2 | HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.156+7058G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436943 | ||||||
chr3:100437225
|
T | C | 1 | a0002c0002t0003g0374 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.156+7340T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437225 | ||||||
chr3:100437693
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+7808T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437693 | ||||||
chr3:100437860
|
A | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(77): Show | 88 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.156+7975A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437860 | ||||||
chr3:100437879
|
C | A | 7 | a0002c0002t0003g0102a0002c0002t0003g0122a0002c0002t0003g0128others(4): Show | 7 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+7994C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437879 | ||||||
chr3:100437956
|
G | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+8071G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437956 | ||||||
chr3:100438172
|
A | G | 10 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(7): Show | 10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+8287A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438172 | ||||||
chr3:100438214
|
A | T | 1 | a0001c0001t0001g0073 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.156+8329A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438214 | ||||||
chr3:100438288
|
T | G | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(338): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.156+8403T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438288 | ||||||
chr3:100438684
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+8799A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438684 | ||||||
chr3:100438744
|
A | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.156+8859A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438744 | ||||||
chr3:100438869
|
G | C | 2 | a0001c0001t0003g0143a0001c0001t0003g0144 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+8984G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438869 | ||||||
chr3:100438874
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.156+8989G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438874 | ||||||
chr3:100438917
|
T | C | 1 | a0002c0002t0001g0043 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.156+9032T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438917 | ||||||
chr3:100438938
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.156+9053G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438938 | ||||||
chr3:100438940
|
G | T | 6 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(3): Show | 6 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+9055G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438940 | ||||||
chr3:100438982
|
A | AT | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+9103dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100438982 | |||||
chr3:100438991
|
G | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+9106G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438991 | ||||||
chr3:100439000
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9115C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439000 | ||||||
chr3:100439063
|
C | T | 1 | a0001c0001t0002g0371 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.156+9178C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439063 | ||||||
chr3:100439129
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9244A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439129 | ||||||
chr3:100439160
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0153others(1): Show | 5 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+9275T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439160 | ||||||
chr3:100439238
|
A | G | 4 | a0002c0002t0004g0076a0002c0002t0004g0077a0002c0002t0004g0078others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+9353A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439238 | ||||||
chr3:100439251
|
T | A | 1 | a0002c0002t0003g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.156+9366T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439251 | ||||||
chr3:100439267
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9382C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439267 | ||||||
chr3:100439268
|
G | A | 1 | a0001c0001t0002g0350 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156+9383G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439268 | ||||||
chr3:100439277
|
TAA | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9402_156+9403d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100439277 | |||||
chr3:100439340
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9455C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439340 | ||||||
chr3:100439346
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+9461T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439346 | ||||||
chr3:100439490
|
T | G | 1 | a0002c0002t0013g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.156+9605T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439490 | ||||||
chr3:100439556
|
C | T | 1 | a0002c0002t0012g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.156+9671C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439556 | ||||||
chr3:100439558
|
T | C | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(70): Show | 81 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.156+9673T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439558 | ||||||
chr3:100439562
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9677G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439562 | ||||||
chr3:100439610
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9725C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439610 | ||||||
chr3:100439849
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(17): Show | 21 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.156+9964G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439849 | ||||||
chr3:100439868
|
T | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(17): Show | 21 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.156+9983T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439868 | ||||||
chr3:100440257
|
A | T | 10 | a0002c0002t0001g0035a0002c0002t0001g0158a0002c0002t0001g0195others(7): Show | 10 | HG00735.hp1 HG01106.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+10372A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440257 | ||||||
chr3:100440390
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156+10505T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440390 | ||||||
chr3:100440489
|
C | T | 1 | a0001c0001t0002g0345 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.156+10604C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440489 | ||||||
chr3:100440842
|
A | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(58): Show | 68 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.157-10877A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440842 | ||||||
chr3:100440916
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-10803C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440916 | ||||||
chr3:100440924
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-10795T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440924 | ||||||
chr3:100440973
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-10746G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440973 | ||||||
chr3:100441052
|
G | C | 1 | a0002c0002t0003g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.157-10667G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441052 | ||||||
chr3:100441064
|
A | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-10655A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441064 | ||||||
chr3:100441123
|
G | C | 13 | a0001c0004t0004g0203a0002c0002t0004g0025a0002c0002t0004g0076others(10): Show | 13 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.157-10596G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441123 | ||||||
chr3:100441337
|
G | A | 12 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(9): Show | 12 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-10382G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441337 | ||||||
chr3:100441356
|
G | C | 1 | a0002c0002t0011g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157-10363G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441356 | ||||||
chr3:100441450
|
A | G | 3 | a0001c0004t0004g0203a0002c0002t0003g0098a0002c0002t0003g0145 | 3 | HG02257.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.157-10269A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441450 | ||||||
chr3:100441461
|
T | C | 1 | a0001c0001t0002g0357 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.157-10258T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441461 | ||||||
chr3:100441631
|
A | AAT | 3 | a0002c0002t0001g0206a0002c0002t0001g0248a0002c0002t0003g0146 | 3 | HG01175.hp2 HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.157-10069_157-1006 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100441631 | |||||
chr3:100441631
|
AAT | A | 134 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 142 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.157-10069_157-1006 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100441631 | |||||
chr3:100441631
|
AATAT | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 172 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.157-10071_157-1006 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100441631 | |||||
chr3:100441697
|
C | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-10022C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441697 | ||||||
chr3:100441722
|
G | A | 1 | a0002c0003t0010g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.157-9997G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441722 | ||||||
chr3:100442291
|
A | ATGTGAAC others(1): Show |
6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0211others(3): Show | 6 | NA18946.hp2 NA18947.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-9427_157-9420d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100442291 | |||||
chr3:100442362
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.157-9357G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442362 | ||||||
chr3:100442401
|
G | C | 1 | a0002c0002t0003g0132 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.157-9318G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442401 | ||||||
chr3:100442557
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.157-9162T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442557 | ||||||
chr3:100442775
|
T | A | 3 | a0002c0002t0001g0273a0002c0002t0003g0098a0002c0002t0003g0145 | 3 | HG02257.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.157-8944T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442775 | ||||||
chr3:100442927
|
C | T | 10 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(7): Show | 10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-8792C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442927 | ||||||
chr3:100442935
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0235a0001c0001t0002g0359others(1): Show | 4 | HG03688.hp1 NA18950.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-8784A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442935 | ||||||
chr3:100443014
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-8705A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443014 | ||||||
chr3:100443027
|
C | T | 4 | a0002c0002t0001g0253a0002c0002t0001g0259a0002c0002t0001g0292others(1): Show | 4 | HG02040.hp2 HG02083.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-8692C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443027 | ||||||
chr3:100443038
|
T | C | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-8681T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443038 | ||||||
chr3:100443123
|
G | A | 2 | a0002c0002t0004g0149a0002c0002t0004g0150 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.157-8596G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443123 | ||||||
chr3:100443173
|
T | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-8546T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443173 | ||||||
chr3:100443402
|
G | A | 1 | a0001c0004t0004g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157-8317G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443402 | ||||||
chr3:100443511
|
TTAA | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-8207_157-8205d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443511 | ||||||
chr3:100443533
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.157-8186C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443533 | ||||||
chr3:100443534
|
G | A | 1 | a0002c0002t0004g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.157-8185G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443534 | ||||||
chr3:100443547
|
T | G | 3 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0057 | 3 | HG00558.hp1 HG00609.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.157-8172T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443547 | ||||||
chr3:100443652
|
C | T | 1 | a0002c0002t0001g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.157-8067C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443652 | ||||||
chr3:100443912
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-7807T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443912 | ||||||
chr3:100444037
|
A | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.157-7682A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444037 | ||||||
chr3:100444176
|
T | A | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-7543T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444176 | ||||||
chr3:100444203
|
C | A | 1 | a0001c0001t0002g0017 | 2 | NA18960.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.157-7516C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444203 | ||||||
chr3:100444273
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-7446C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444273 | ||||||
chr3:100444563
|
T | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-7156T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444563 | ||||||
chr3:100444593
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.157-7126A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444593 | ||||||
chr3:100444672
|
A | G | 1 | a0001c0001t0002g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.157-7047A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444672 | ||||||
chr3:100444755
|
C | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-6964C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444755 | ||||||
chr3:100444860
|
A | G | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-6859A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444860 | ||||||
chr3:100445194
|
C | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(39): Show | 48 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-6525C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445194 | ||||||
chr3:100445417
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.157-6302A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445417 | ||||||
chr3:100445572
|
G | A | 12 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(9): Show | 12 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-6147G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445572 | ||||||
chr3:100445678
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.157-6041A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445678 | ||||||
chr3:100445793
|
C | T | 364 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(361): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.157-5926C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445793 | ||||||
chr3:100445906
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.157-5813C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445906 | ||||||
chr3:100446005
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(6): Show | 10 | HG00140.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-5714G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446005 | ||||||
chr3:100446155
|
A | C | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-5564A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446155 | ||||||
chr3:100446278
|
G | A | 10 | a0002c0002t0001g0035a0002c0002t0001g0158a0002c0002t0001g0195others(7): Show | 10 | HG00735.hp1 HG01106.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-5441G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446278 | ||||||
chr3:100446316
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.157-5403C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446316 | ||||||
chr3:100446341
|
A | C | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157-5378A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446341 | ||||||
chr3:100446347
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157-5372A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446347 | ||||||
chr3:100446365
|
A | C | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.157-5354A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446365 | ||||||
chr3:100446406
|
G | A | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-5313G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446406 | ||||||
chr3:100446546
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157-5173A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446546 | ||||||
chr3:100446578
|
AC | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-5140delC | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446578 | ||||||
chr3:100446694
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.157-5025C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446694 | ||||||
chr3:100446715
|
A | C | 1 | a0001c0001t0002g0371 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.157-5004A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446715 | ||||||
chr3:100446781
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-4938G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446781 | ||||||
chr3:100446861
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157-4858C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446861 | ||||||
chr3:100446995
|
TTGG | T | 13 | a0001c0004t0004g0203a0002c0002t0004g0025a0002c0002t0004g0076others(10): Show | 13 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.157-4720_157-4718d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100446995 | |||||
chr3:100447031
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.157-4688G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447031 | ||||||
chr3:100447061
|
A | G | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(42): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-4658A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447061 | ||||||
chr3:100447262
|
T | C | 1 | a0002c0002t0003g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.157-4457T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447262 | ||||||
chr3:100447368
|
A | G | 7 | a0002c0002t0003g0102a0002c0002t0003g0122a0002c0002t0003g0128others(4): Show | 7 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-4351A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447368 | ||||||
chr3:100447391
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-4328T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447391 | ||||||
chr3:100447391
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 31 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.157-4328T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447391 | ||||||
chr3:100447432
|
C | T | 1 | a0002c0002t0001g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.157-4287C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447432 | ||||||
chr3:100447503
|
G | A | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.157-4216G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447503 | ||||||
chr3:100447614
|
TA | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.157-4095delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100447614 | |||||
chr3:100448098
|
A | AGATT | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.157-3621_157-3620i others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448098 | ||||||
chr3:100448130
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.157-3589C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448130 | ||||||
chr3:100448131
|
G | A | 10 | a0002c0002t0001g0035a0002c0002t0001g0158a0002c0002t0001g0195others(7): Show | 10 | HG00735.hp1 HG01106.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-3588G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448131 | ||||||
chr3:100448158
|
AACTGAGA others(21): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-3555_157-3528d others(30): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100448158 | |||||
chr3:100448802
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.157-2917C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448802 | ||||||
chr3:100448865
|
G | GT | 6 | a0001c0001t0001g0218a0001c0001t0001g0227a0001c0001t0001g0236others(3): Show | 6 | HG03927.hp2 HG04184.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-2846dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100448865 | |||||
chr3:100448952
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.157-2767A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448952 | ||||||
chr3:100448999
|
A | G | 1 | a0001c0001t0001g0369 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.157-2720A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448999 | ||||||
chr3:100449007
|
A | G | 372 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(369): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.157-2712A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449007 | ||||||
chr3:100449144
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 31 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.157-2575C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449144 | ||||||
chr3:100449241
|
A | G | 3 | a0001c0001t0002g0312a0001c0001t0002g0321a0001c0001t0002g0325 | 3 | HG00741.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.157-2478A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449241 | ||||||
chr3:100449248
|
CT | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(100): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.157-2458delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100449248 | |||||
chr3:100449386
|
G | A | 1 | a0001c0001t0001g0014 | 2 | HG00673.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.157-2333G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449386 | ||||||
chr3:100449468
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.157-2251C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449468 | ||||||
chr3:100449469
|
G | A | 1 | a0002c0002t0003g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.157-2250G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449469 | ||||||
chr3:100449729
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1990C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449729 | ||||||
chr3:100449832
|
T | C | 1 | a0002c0002t0001g0253 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.157-1887T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449832 | ||||||
chr3:100449921
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.157-1798C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449921 | ||||||
chr3:100450089
|
C | CT | 14 | a0002c0002t0001g0206a0002c0002t0001g0256a0002c0002t0001g0274others(11): Show | 14 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.157-1612dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450089 | |||||
chr3:100450089
|
CTT | C | 11 | a0001c0004t0004g0203a0002c0002t0004g0025a0002c0002t0004g0076others(8): Show | 11 | HG02145.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-1613_157-1612d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450089 | |||||
chr3:100450089
|
CTTTT | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.157-1615_157-1612d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450089 | |||||
chr3:100450117
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.157-1602G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450117 | ||||||
chr3:100450247
|
T | TA | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1465dupA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450247 | |||||
chr3:100450249
|
A | AAAAAACA others(13): Show |
7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-1468_157-1449d others(22): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450249 | |||||
chr3:100450332
|
AT | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0223a0001c0001t0001g0225others(9): Show | 12 | HG01106.hp1 HG01934.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-1369delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450332 | |||||
chr3:100450426
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.157-1293T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450426 | ||||||
chr3:100450584
|
G | A | 1 | a0002c0002t0003g0126 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.157-1135G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450584 | ||||||
chr3:100450678
|
A | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0075others(15): Show | 20 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.157-1041A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450678 | ||||||
chr3:100450828
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.157-891T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450828 | ||||||
chr3:100450882
|
A | AAAAT | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-819_157-816dup others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450882 | |||||
chr3:100450902
|
TAGAG | T | 4 | a0002c0002t0001g0035a0002c0002t0001g0195a0002c0002t0001g0196others(1): Show | 4 | HG01106.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-808_157-805del others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450902 | |||||
chr3:100451187
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.157-532A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451187 | ||||||
chr3:100451280
|
C | T | 1 | a0002c0002t0012g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.157-439C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451280 | ||||||
chr3:100451313
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.157-406C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451313 | ||||||
chr3:100451389
|
A | G | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-330A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451389 | ||||||
chr3:100451423
|
T | G | 1 | a0001c0001t0002g0336 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.157-296T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451423 | ||||||
chr3:100451614
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-105A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451614 | ||||||
chr3:100451709
|
G | A | 57 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0008others(54): Show | 62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.157-10G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451709 | ||||||
chr3:100451981
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.387+32G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100451981 | ||||||
chr3:100452147
|
G | A | 10 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(7): Show | 10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+198G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452147 | ||||||
chr3:100452202
|
C | CT | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(78): Show | 87 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.387+271dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452202 | |||||
chr3:100452202
|
C | CTT | 20 | a0001c0001t0006g0233a0002c0002t0001g0047a0002c0002t0001g0242others(17): Show | 20 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.387+270_387+271dup others(2): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452202 | |||||
chr3:100452202
|
CT | C | 6 | a0001c0001t0001g0051a0001c0001t0001g0246a0001c0004t0004g0203others(3): Show | 6 | HG01169.hp1 HG02015.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+271delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452202 | |||||
chr3:100452206
|
T | C | 2 | a0002c0002t0001g0003a0002c0002t0001g0054 | 4 | NA18961.hp2 NA18966.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+257T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452206 | ||||||
chr3:100452333
|
G | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+384G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452333 | ||||||
chr3:100452397
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0151others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+448G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452397 | ||||||
chr3:100452629
|
C | CTAG | 3 | a0002c0002t0004g0164a0002c0002t0004g0192a0002c0002t0008g0165 | 3 | HG02615.hp2 HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.387+681_387+682ins others(3): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452629 | |||||
chr3:100452741
|
G | A | 1 | a0002c0002t0003g0093 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.387+792G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452741 | ||||||
chr3:100452823
|
C | G | 1 | a0001c0001t0001g0001 | 3 | NA18988.hp1 NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.387+874C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452823 | ||||||
chr3:100452922
|
CT | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.387+980delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452922 | |||||
chr3:100453081
|
G | A | 32 | a0002c0002t0001g0047a0002c0002t0001g0206a0002c0002t0001g0242others(29): Show | 32 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.387+1132G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453081 | ||||||
chr3:100453086
|
G | A | 6 | a0002c0002t0004g0025a0002c0002t0004g0076a0002c0002t0004g0077others(3): Show | 6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1137G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453086 | ||||||
chr3:100453271
|
T | C | 1 | a0002c0002t0003g0094 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.387+1322T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453271 | ||||||
chr3:100453354
|
C | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.387+1405C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453354 | ||||||
chr3:100453398
|
T | C | 1 | a0002c0002t0001g0185 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.387+1449T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453398 | ||||||
chr3:100453424
|
TA | T | 12 | a0001c0001t0001g0037a0001c0001t0001g0080a0001c0001t0001g0216others(9): Show | 12 | HG01167.hp2 HG01496.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.387+1492delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100453424 | |||||
chr3:100453425
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A | T | 1 | a0002c0002t0001g0057 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.387+1476A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453425 | ||||||
chr3:100453515
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G | A | 2 | a0002c0002t0001g0163a0002c0002t0001g0182 | 2 | NA19072.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.387+1566G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453515 | ||||||
chr3:100453523
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G | A | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+1574G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453523 | ||||||
chr3:100453578
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.387+1629G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453578 | ||||||
chr3:100453584
|
C | CA | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 63 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.387+1650dupA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100453584 | |||||
chr3:100453584
|
CA | C | 7 | a0001c0001t0001g0246a0001c0001t0002g0309a0002c0002t0001g0050others(4): Show | 7 | HG00323.hp2 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+1650delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100453584 | |||||
chr3:100453627
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A | T | 1 | a0001c0001t0001g0285 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.387+1678A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453627 | ||||||
chr3:100453888
|
C | G | 1 | a0001c0001t0001g0367 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.388-1889C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453888 | ||||||
chr3:100454463
|
C | T | 3 | a0001c0001t0002g0306a0001c0001t0002g0317a0001c0001t0002g0324 | 3 | NA18964.hp2 NA18965.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.388-1314C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454463 | ||||||
chr3:100454631
|
A | T | 2 | a0001c0001t0002g0321a0001c0001t0002g0325 | 2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.388-1146A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454631 | ||||||
chr3:100454681
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.388-1096C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454681 | ||||||
chr3:100454769
|
T | C | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-1008T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454769 | ||||||
chr3:100454827
|
C | T | 2 | a0002c0002t0003g0098a0002c0002t0003g0145 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.388-950C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454827 | ||||||
chr3:100454903
|
T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0369a0001c0001t0001g0370 | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-874T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454903 | ||||||
chr3:100455006
|
C | G | 69 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0034others(66): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.388-771C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455006 | ||||||
chr3:100455293
|
C | T | 1 | a0002c0002t0001g0293 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388-484C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455293 | ||||||
chr3:100455317
|
G | A | 1 | a0002c0002t0004g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388-460G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455317 | ||||||
chr3:100455377
|
A | G | 58 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0008others(55): Show | 63 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.388-400A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455377 | ||||||
chr3:100455610
|
G | A | 5 | a0002c0002t0001g0158a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-167G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455610 | ||||||
chr3:100455683
|
A | G | 1 | a0001c0001t0005g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.388-94A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455683 | ||||||
chr3:100455751
|
A | C | 7 | a0001c0001t0005g0074a0001c0001t0005g0295a0001c0001t0005g0296others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-26A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455751 |