geneid | 64127 |
---|---|
ensemblid | ENSG00000167207.15 |
hgncid | 5331 |
symbol | NOD2 |
name | nucleotide binding oligomerization domain containing 2 |
refseq_nuc | NM_001370466.1 |
refseq_prot | NP_001357395.1 |
ensembl_nuc | ENST00000647318.2 |
ensembl_prot | ENSP00000495993.1 |
mane_status | MANE Select |
chr | chr16 |
start | 50693606 |
end | 50733075 |
strand | + |
ver | v1.2 |
region | chr16:50693606-50733075 |
region5000 | chr16:50688606-50738075 |
regionname0 | NOD2_chr16_50693606_50733075 |
regionname5000 | NOD2_chr16_50688606_50738075 |
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 | 1/1 | 1013 | 249 | 72 | 47 | 97 | 10 | 21 | 78 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0002 | 0/0 | 1013 | 18 | 2 | 10 | 1 | 1 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0003 | 0/0 | 1013 | 10 | 0 | 6 | 0 | 4 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0004 | 0/0 | 1013 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0005 | 0/0 | 1013 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0006 | 0/0 | 1013 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0007 | 0/0 | 1013 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0008 | 0/0 | 1013 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0009 | 0/0 | 1013 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0010 | 0/0 | 1013 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0011 | 0/0 | 1013 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0012 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0013 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0014 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0015 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0016 | 0/0 | 1013 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0017 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0018 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0019 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0020 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
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 | 1/0 | 3042 | 153 | 38 | 28 | 66 | 5 | 15 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0002 | 0/0 | 3042 | 35 | 8 | 3 | 23 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0003 | 0/0 | 3042 | 30 | 19 | 3 | 7 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0004 | 0/0 | 3042 | 27 | 5 | 13 | 0 | 4 | 5 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0005 | 0/0 | 3042 | 18 | 2 | 10 | 1 | 1 | 4 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0006 | 0/0 | 3042 | 10 | 0 | 6 | 0 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0007 | 0/0 | 3042 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0008 | 0/0 | 3042 | 4 | 4 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0009 | 0/0 | 3042 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0010 | 0/0 | 3042 | 3 | 0 | 2 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0011 | 0/0 | 3042 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0012 | 0/0 | 3042 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0013 | 0/0 | 3042 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0014 | 0/0 | 3042 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0015 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0016 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0017 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0018 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0019 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0020 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0021 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0022 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0023 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0024 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0025 | 0/1 | 3042 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0026 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0027 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
c0028 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
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 | 1/1 | 1322 | 168 | 32 | 46 | 63 | 7 | 18 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0002 | 0/0 | 1322 | 127 | 54 | 22 | 34 | 11 | 6 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0003 | 0/0 | 1322 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0004 | 0/0 | 1322 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0005 | 0/0 | 1322 | 3 | 0 | 2 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0006 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0007 | 0/0 | 1300 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0008 | 0/0 | 1322 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0009 | 0/0 | 1322 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
t0010 | 0/0 | 1322 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
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 | 10 | 0 | 7 | 0 | 1 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0002 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0003 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0005 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0013 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0037 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
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 | 1/0 | 3042 | 153 | 38 | 28 | 66 | 5 | 15 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0002 | 0/0 | 3042 | 35 | 8 | 3 | 23 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0003 | 0/0 | 3042 | 30 | 19 | 3 | 7 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0004 | 0/0 | 3042 | 27 | 5 | 13 | 0 | 4 | 5 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0018 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0019 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0025 | 0/1 | 3042 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0027 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0002c0005 | 0/0 | 3042 | 18 | 2 | 10 | 1 | 1 | 4 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0003c0006 | 0/0 | 3042 | 10 | 0 | 6 | 0 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0004c0007 | 0/0 | 3042 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0005c0008 | 0/0 | 3042 | 4 | 4 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0005c0026 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0006c0011 | 0/0 | 3042 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0007c0009 | 0/0 | 3042 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0008c0010 | 0/0 | 3042 | 3 | 0 | 2 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0009c0014 | 0/0 | 3042 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0010c0013 | 0/0 | 3042 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0011c0012 | 0/0 | 3042 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0012c0016 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0013c0023 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0014c0024 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0015c0017 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0016c0020 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0017c0028 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0018c0021 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0019c0022 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0020c0015 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4363 | 126 | 21 | 27 | 58 | 5 | 14 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0002 | 0/0 | 4363 | 19 | 13 | 1 | 5 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0004 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0005 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0006 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0007 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0008 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0001t0010 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0002t0002 | 0/0 | 4363 | 35 | 8 | 3 | 23 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0003t0001 | 0/0 | 4363 | 11 | 8 | 2 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0003t0002 | 0/0 | 4363 | 13 | 5 | 1 | 6 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0003t0003 | 0/0 | 4363 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0004t0002 | 0/0 | 4363 | 25 | 5 | 11 | 0 | 4 | 5 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0004t0005 | 0/0 | 4363 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0018t0001 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0019t0001 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0025t0001 | 0/1 | 4363 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0001c0027t0002 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0002c0005t0001 | 0/0 | 4363 | 17 | 2 | 10 | 1 | 1 | 3 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0002c0005t0009 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0003c0006t0002 | 0/0 | 4363 | 10 | 0 | 6 | 0 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0004c0007t0002 | 0/0 | 4363 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0005c0008t0002 | 0/0 | 4363 | 4 | 4 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0005c0026t0002 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0006c0011t0002 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0007c0009t0002 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0008c0010t0001 | 0/0 | 4363 | 3 | 0 | 2 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0009c0014t0002 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0010c0013t0001 | 0/0 | 4363 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0011c0012t0002 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0012c0016t0001 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0013c0023t0002 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0014c0024t0002 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0015c0017t0001 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0016c0020t0002 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0017c0028t0001 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0018c0021t0001 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0019c0022t0001 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
a0020c0015t0001 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | copy fasta | chr16 | 50688606 | 50738075 |
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 | 10 | 0 | 7 | 0 | 1 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0037 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0013 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0003 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0004t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0018t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0019t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0025t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0001c0027t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0002c0005t0009g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0003c0006t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0004c0007t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0004c0007t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0004c0007t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0004c0007t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0004c0007t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0004c0007t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0005c0008t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0005c0008t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0005c0008t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0005c0008t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0005c0026t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0006c0011t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0006c0011t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0006c0011t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0007c0009t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0007c0009t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0008c0010t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0008c0010t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0008c0010t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0009c0014t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0010c0013t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0010c0013t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0011c0012t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0011c0012t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0012c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0013c0023t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0014c0024t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0015c0017t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0016c0020t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0017c0028t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0018c0021t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0019c0022t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
a0020c0015t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0023 | t0002 | g0053 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00140 | hp1 | a0003 | c0006 | t0002 | g0025 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00140 | hp2 | a0001 | c0004 | t0002 | g0084 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00280 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00280 | hp2 | a0001 | c0004 | t0002 | g0098 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00323 | hp1 | a0001 | c0004 | t0002 | g0003 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00408 | hp2 | a0001 | c0018 | t0001 | g0002 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00642 | hp1 | a0002 | c0005 | t0001 | g0004 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00733 | hp1 | a0002 | c0005 | t0001 | g0198 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00735 | hp1 | a0008 | c0010 | t0001 | g0021 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00735 | hp2 | a0001 | c0004 | t0002 | g0086 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00738 | hp1 | a0001 | c0004 | t0002 | g0085 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG00738 | hp2 | a0008 | c0010 | t0001 | g0067 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01070 | hp1 | a0002 | c0005 | t0001 | g0204 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01071 | hp2 | a0002 | c0005 | t0001 | g0205 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01074 | hp1 | a0001 | c0004 | t0002 | g0089 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01074 | hp2 | a0002 | c0005 | t0001 | g0201 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01081 | hp1 | a0002 | c0005 | t0001 | g0019 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01081 | hp2 | a0003 | c0006 | t0002 | g0075 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01099 | hp2 | a0003 | c0006 | t0002 | g0101 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01106 | hp2 | a0001 | c0004 | t0002 | g0026 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0081 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01109 | hp2 | a0017 | c0028 | t0001 | g0200 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01168 | hp1 | a0001 | c0004 | t0005 | g0028 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01168 | hp2 | a0003 | c0006 | t0002 | g0090 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01169 | hp2 | a0001 | c0004 | t0005 | g0028 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01175 | hp1 | a0002 | c0005 | t0001 | g0007 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01192 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01243 | hp1 | a0018 | c0021 | t0001 | g0004 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01255 | hp1 | a0003 | c0006 | t0002 | g0043 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01255 | hp2 | a0010 | c0013 | t0001 | g0004 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01256 | hp2 | a0003 | c0006 | t0002 | g0043 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01261 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01361 | hp2 | a0002 | c0005 | t0001 | g0020 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01433 | hp1 | a0010 | c0013 | t0001 | g0063 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01496 | hp2 | a0001 | c0004 | t0002 | g0087 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01515 | hp1 | a0003 | c0006 | t0002 | g0206 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01515 | hp2 | a0014 | c0024 | t0002 | g0088 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01516 | hp1 | a0002 | c0005 | t0001 | g0020 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01517 | hp2 | a0003 | c0006 | t0002 | g0207 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0024 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01884 | hp2 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01891 | hp2 | a0004 | c0007 | t0002 | g0071 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01943 | hp1 | a0001 | c0004 | t0002 | g0025 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01952 | hp2 | a0001 | c0004 | t0002 | g0095 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01981 | hp1 | a0002 | c0005 | t0001 | g0019 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01993 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02056 | hp2 | a0002 | c0005 | t0001 | g0007 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02145 | hp2 | a0005 | c0008 | t0002 | g0216 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02257 | hp1 | a0009 | c0014 | t0002 | g0033 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02258 | hp1 | a0001 | c0004 | t0002 | g0105 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0094 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02273 | hp2 | a0001 | c0004 | t0002 | g0102 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02280 | hp1 | a0007 | c0009 | t0002 | g0022 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02300 | hp2 | a0002 | c0005 | t0001 | g0208 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0065 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02602 | hp2 | a0008 | c0010 | t0001 | g0066 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02622 | hp1 | a0001 | c0003 | t0002 | g0024 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02630 | hp1 | a0011 | c0012 | t0002 | g0070 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02630 | hp2 | a0005 | c0026 | t0002 | g0044 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0108 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0211 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0210 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02723 | hp1 | a0011 | c0012 | t0002 | g0069 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02723 | hp2 | a0006 | c0011 | t0002 | g0093 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02738 | hp1 | a0001 | c0004 | t0002 | g0054 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02818 | hp1 | a0001 | c0003 | t0003 | g0055 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02818 | hp2 | a0001 | c0027 | t0002 | g0096 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02886 | hp1 | a0006 | c0011 | t0002 | g0091 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02895 | hp2 | a0004 | c0007 | t0002 | g0111 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02896 | hp2 | a0001 | c0019 | t0001 | g0064 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02922 | hp2 | a0001 | c0004 | t0002 | g0125 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02970 | hp2 | a0005 | c0008 | t0002 | g0214 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03017 | hp1 | a0001 | c0004 | t0002 | g0027 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03041 | hp2 | a0002 | c0005 | t0001 | g0197 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03098 | hp1 | a0007 | c0009 | t0002 | g0068 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03130 | hp1 | a0004 | c0007 | t0002 | g0073 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03139 | hp2 | a0016 | c0020 | t0002 | g0169 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03195 | hp1 | a0001 | c0004 | t0002 | g0106 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03239 | hp1 | a0001 | c0004 | t0002 | g0097 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03453 | hp1 | a0009 | c0014 | t0002 | g0033 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03453 | hp2 | a0004 | c0007 | t0002 | g0072 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03540 | hp2 | a0002 | c0005 | t0001 | g0199 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03654 | hp1 | a0002 | c0005 | t0009 | g0007 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03669 | hp1 | a0001 | c0004 | t0002 | g0027 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03688 | hp2 | a0002 | c0005 | t0001 | g0192 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG04115 | hp1 | a0001 | c0004 | t0002 | g0003 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0104 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG04228 | hp2 | a0002 | c0005 | t0001 | g0021 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18906 | hp2 | a0005 | c0008 | t0002 | g0044 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18947 | hp2 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18950 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18979 | hp1 | a0001 | c0001 | t0010 | g0156 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18995 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19002 | hp1 | a0020 | c0015 | t0001 | g0035 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19002 | hp2 | a0001 | c0003 | t0002 | g0083 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19011 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19030 | hp2 | a0006 | c0011 | t0002 | g0092 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0107 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19057 | hp1 | a0015 | c0017 | t0001 | g0014 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19062 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19080 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19083 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ASW | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20752 | hp1 | a0012 | c0016 | t0001 | g0004 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20752 | hp2 | a0001 | c0004 | t0002 | g0099 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20805 | hp1 | a0003 | c0006 | t0002 | g0003 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01123 | hp1 | a0003 | c0006 | t0002 | g0003 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG01123 | hp2 | a0019 | c0022 | t0001 | g0004 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02109 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02486 | hp1 | a0007 | c0009 | t0002 | g0022 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG02559 | hp2 | a0005 | c0008 | t0002 | g0215 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG03471 | hp2 | a0001 | c0004 | t0002 | g0103 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG06807 | hp1 | a0004 | c0007 | t0002 | g0183 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA20300 | hp2 | a0004 | c0007 | t0002 | g0110 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
homoSapiens_chm13v2 | hp1 | a0001 | c0025 | t0001 | g0202 | REF | REF | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0037 | REF | REF | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50699742
|
G | A | 1 | a0020 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.247G>A | p.Ala83Thr | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 312/4363 | 247/3042 | 83/1013 | chr16 | 50699742 | ||
chr16:50699827
|
G | A | 1 | a0012 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.332G>A | p.Arg111Gln | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 397/4363 | 332/3042 | 111/1013 | chr16 | 50699827 | ||
chr16:50699832
|
G | A | 1 | a0011 | 2 | HG02630.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.337G>A | p.Ala113Thr | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 402/4363 | 337/3042 | 113/1013 | chr16 | 50699832 | ||
chr16:50707880
|
C | T | 1 | a0009 | 2 | HG02257.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.485C>T | p.Thr162Met | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/12 | 550/4363 | 485/3042 | 162/1013 | chr16 | 50707880 | ||
chr16:50710713
|
C | T | 7 | a0002a0008a0010others(4): Show | 27 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
missense_variant | MODERATE | c.721C>T | p.Pro241Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 786/4363 | 721/3042 | 241/1013 | chr16 | 50710713 | ||
chr16:50710786
|
C | T | 1 | a0016 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.794C>T | p.Ala265Val | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 859/4363 | 794/3042 | 265/1013 | chr16 | 50710786 | ||
chr16:50710966
|
A | G | 1 | a0007 | 3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.974A>G | p.His325Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1039/4363 | 974/3042 | 325/1013 | chr16 | 50710966 | ||
chr16:50711196
|
G | A | 1 | a0015 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1204G>A | p.Ala402Thr | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1269/4363 | 1204/3042 | 402/1013 | chr16 | 50711196 | ||
chr16:50711685
|
G | A | 1 | a0017 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1693G>A | p.Val565Met | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1758/4363 | 1693/3042 | 565/1013 | chr16 | 50711685 | ||
chr16:50711845
|
C | G | 1 | a0014 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1853C>G | p.Pro618Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1918/4363 | 1853/3042 | 618/1013 | chr16 | 50711845 | ||
chr16:50711962
|
G | A | 1 | a0006 | 3 | HG02723.hp2 HG02886.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.1970G>A | p.Arg657Gln | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2035/4363 | 1970/3042 | 657/1013 | chr16 | 50711962 | ||
chr16:50712015
|
C | T | 1 | a0010 | 2 | HG01255.hp2 HG01433.hp1 |
missense_variant | MODERATE | c.2023C>T | p.Arg675Trp | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2088/4363 | 2023/3042 | 675/1013 | chr16 | 50712015 | ||
chr16:50712018
|
C | T | 1 | a0013 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2026C>T | p.Arg676Cys | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2091/4363 | 2026/3042 | 676/1013 | chr16 | 50712018 | ||
chr16:50712085
|
C | G | 1 | a0005 | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.2093C>G | p.Ala698Gly | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2158/4363 | 2093/3042 | 698/1013 | chr16 | 50712085 | ||
chr16:50712280
|
G | A | 1 | a0004 | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.2288G>A | p.Arg763Gln | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2353/4363 | 2288/3042 | 763/1013 | chr16 | 50712280 | ||
chr16:50716899
|
A | G | 1 | a0019 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2474A>G | p.Asn825Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/12 | 2539/4363 | 2474/3042 | 825/1013 | chr16 | 50716899 | ||
chr16:50716931
|
A | G | 1 | a0018 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2506A>G | p.Met836Val | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/12 | 2571/4363 | 2506/3042 | 836/1013 | chr16 | 50716931 | ||
chr16:50722629
|
G | C | 1 | a0008 | 3 | HG00735.hp1 HG00738.hp2 HG02602.hp2 |
missense_variant | MODERATE | c.2641G>C | p.Gly881Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/12 | 2706/4363 | 2641/3042 | 881/1013 | chr16 | 50722629 | ||
chr16:50723365
|
G | A | 1 | a0003 | 10 | HG00140.hp1 HG01081.hp2 HG01099.hp2 others(7): Show |
missense_variant | MODERATE | c.2782G>A | p.Val928Ile | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/12 | 2847/4363 | 2782/3042 | 928/1013 | chr16 | 50723365 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50699753
|
C | T | 1 | a0017c0028 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.258C>T | p.Asp86Asp | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 323/4363 | 258/3042 | 86/1013 | chr16 | 50699753 | ||
chr16:50699948
|
C | G | 9 | a0001c0003a0001c0004a0001c0025others(6): Show | 75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
synonymous_variant | LOW | c.453C>G | p.Ser151Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 518/4363 | 453/3042 | 151/1013 | chr16 | 50699948 | ||
chr16:50710727
|
C | T | 1 | a0001c0027 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.735C>T | p.Ser245Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 800/4363 | 735/3042 | 245/1013 | chr16 | 50710727 | ||
chr16:50711192
|
G | A | 1 | a0009c0014 | 2 | HG02257.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.1200G>A | p.Pro400Pro | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1265/4363 | 1200/3042 | 400/1013 | chr16 | 50711192 | ||
chr16:50711288
|
C | T | 8 | a0001c0019a0002c0005a0008c0010others(5): Show | 28 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
synonymous_variant | LOW | c.1296C>T | p.Arg432Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1361/4363 | 1296/3042 | 432/1013 | chr16 | 50711288 | ||
chr16:50711364
|
C | T | 1 | a0004c0007 | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
synonymous_variant | LOW | c.1372C>T | p.Leu458Leu | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1437/4363 | 1372/3042 | 458/1013 | chr16 | 50711364 | ||
chr16:50711672
|
T | G | 9 | a0001c0002a0001c0004a0001c0025others(6): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
synonymous_variant | LOW | c.1680T>G | p.Arg560Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1745/4363 | 1680/3042 | 560/1013 | chr16 | 50711672 | ||
chr16:50711744
|
C | T | 1 | a0001c0025 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.1752C>T | p.Ala584Ala | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1817/4363 | 1752/3042 | 584/1013 | chr16 | 50711744 | ||
chr16:50716915
|
C | T | 1 | a0001c0018 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2490C>T | p.Asp830Asp | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/12 | 2555/4363 | 2490/3042 | 830/1013 | chr16 | 50716915 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50693632
|
G | C | 1 | a0001c0001t0006 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/12 | 5864 | chr16 | 50693632 | |||||
chr16:50731961
|
A | G | 1 | a0001c0001t0010 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 142 | chr16 | 50731961 | |||||
chr16:50732216
|
A | C | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(17): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 397 | chr16 | 50732216 | |||||
chr16:50732278
|
T | C | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 459 | chr16 | 50732278 | |||||
chr16:50732290
|
C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*471C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 471 | chr16 | 50732290 | |||||
chr16:50732291
|
A | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 472 | chr16 | 50732291 | |||||
chr16:50732292
|
T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*473T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 473 | chr16 | 50732292 | |||||
chr16:50732293
|
C | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 474 | chr16 | 50732293 | |||||
chr16:50732302
|
T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 483 | chr16 | 50732302 | |||||
chr16:50732303
|
C | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 484 | chr16 | 50732303 | |||||
chr16:50732304
|
C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 485 | chr16 | 50732304 | |||||
chr16:50732305
|
C | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 486 | chr16 | 50732305 | |||||
chr16:50732306
|
C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 487 | chr16 | 50732306 | |||||
chr16:50732308
|
T | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*489T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 489 | chr16 | 50732308 | |||||
chr16:50732309
|
C | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 490 | chr16 | 50732309 | |||||
chr16:50732310
|
T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 491 | chr16 | 50732310 | |||||
chr16:50732312
|
T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 493 | chr16 | 50732312 | |||||
chr16:50732314
|
G | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 495 | chr16 | 50732314 | |||||
chr16:50732315
|
TTCCTCCC others(15): Show |
T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498_*519delCCTCCC others(16): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 498 | INFO_REALIGN_3_PRIME | chr16 | 50732315 | ||||
chr16:50732340
|
C | T | 1 | a0001c0003t0003 | 6 | HG01884.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 521 | chr16 | 50732340 | |||||
chr16:50732343
|
A | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 524 | chr16 | 50732343 | |||||
chr16:50732367
|
T | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 548 | chr16 | 50732367 | |||||
chr16:50732371
|
G | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 552 | chr16 | 50732371 | |||||
chr16:50732383
|
C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 564 | chr16 | 50732383 | |||||
chr16:50732389
|
C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 570 | chr16 | 50732389 | |||||
chr16:50732394
|
A | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 575 | chr16 | 50732394 | |||||
chr16:50732395
|
T | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 576 | chr16 | 50732395 | |||||
chr16:50732439
|
G | A | 1 | a0001c0001t0004 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 620 | chr16 | 50732439 | |||||
chr16:50732506
|
C | T | 1 | a0002c0005t0009 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*687C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 687 | chr16 | 50732506 | |||||
chr16:50732565
|
A | C | 1 | a0001c0001t0008 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 746 | chr16 | 50732565 | |||||
chr16:50732975
|
G | A | 18 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(15): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 1156 | chr16 | 50732975 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50693726
|
C | T | 26 | a0001c0001t0002g0017a0001c0001t0002g0227a0001c0002t0002g0006others(23): Show | 35 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9+64C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50693726 | ||||||
chr16:50693877
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+215T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50693877 | ||||||
chr16:50693941
|
T | TG | 29 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0002g0017others(26): Show | 38 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9+282dupG | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50693941 | |||||
chr16:50694107
|
C | T | 1 | a0002c0005t0001g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-9+445C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694107 | ||||||
chr16:50694212
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+550T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694212 | ||||||
chr16:50694502
|
C | T | 3 | a0003c0006t0002g0043a0003c0006t0002g0206a0003c0006t0002g0207 | 4 | HG01255.hp1 HG01256.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+840C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694502 | ||||||
chr16:50694587
|
G | C | 2 | a0001c0004t0002g0054a0013c0023t0002g0053 | 2 | HG00099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-9+925G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694587 | ||||||
chr16:50694695
|
T | G | 27 | a0001c0001t0002g0017a0001c0001t0002g0048a0001c0001t0002g0227others(24): Show | 36 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+1033T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694695 | ||||||
chr16:50694816
|
G | C | 1 | a0001c0003t0003g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+1154G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694816 | ||||||
chr16:50694942
|
T | G | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9+1280T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694942 | ||||||
chr16:50695082
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+1420G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695082 | ||||||
chr16:50695313
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-9+1651G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695313 | ||||||
chr16:50695432
|
A | C | 2 | a0002c0005t0001g0204a0002c0005t0001g0205 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-9+1770A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695432 | ||||||
chr16:50695565
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0203 | 6 | NA18942.hp2 NA18956.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1903A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695565 | ||||||
chr16:50695909
|
A | G | 1 | a0001c0025t0001g0202 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9+2247A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695909 | ||||||
chr16:50696014
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-9+2352T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696014 | ||||||
chr16:50696139
|
G | C | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-9+2477G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696139 | ||||||
chr16:50696177
|
G | T | 5 | a0002c0005t0001g0197a0002c0005t0001g0198a0002c0005t0001g0199others(2): Show | 5 | HG00733.hp1 HG01074.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2515G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696177 | ||||||
chr16:50696318
|
G | A | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0019t0001g0064others(23): Show | 29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+2656G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696318 | ||||||
chr16:50696535
|
G | A | 66 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(63): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9+2873G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696535 | ||||||
chr16:50696628
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-2860T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696628 | ||||||
chr16:50696838
|
G | A | 1 | a0001c0003t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-2650G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696838 | ||||||
chr16:50696954
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-8-2534T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696954 | ||||||
chr16:50696970
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0195a0001c0001t0001g0196 | 4 | HG01167.hp2 HG02145.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2518C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696970 | ||||||
chr16:50697047
|
G | A | 2 | a0004c0007t0002g0110a0004c0007t0002g0111 | 2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-2441G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697047 | ||||||
chr16:50697111
|
T | C | 6 | a0004c0007t0002g0110a0004c0007t0002g0111a0007c0009t0002g0022others(3): Show | 7 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-2377T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697111 | ||||||
chr16:50697185
|
G | A | 31 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0113others(28): Show | 36 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-8-2303G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697185 | ||||||
chr16:50697186
|
T | C | 2 | a0001c0003t0002g0210a0001c0003t0002g0211 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-8-2302T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697186 | ||||||
chr16:50697230
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-2258C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697230 | ||||||
chr16:50697399
|
G | T | 1 | a0008c0010t0001g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-8-2089G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697399 | ||||||
chr16:50697807
|
G | A | 6 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1681G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697807 | ||||||
chr16:50697917
|
T | A | 2 | a0004c0007t0002g0110a0004c0007t0002g0111 | 2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1571T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697917 | ||||||
chr16:50697984
|
G | C | 6 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1504G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697984 | ||||||
chr16:50697992
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG02074.hp1 HG02083.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-8-1496C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697992 | ||||||
chr16:50698115
|
C | T | 4 | a0001c0003t0003g0030a0001c0003t0003g0055a0001c0003t0003g0107others(1): Show | 5 | HG01884.hp2 HG01891.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1373C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698115 | ||||||
chr16:50698197
|
T | C | 2 | a0001c0002t0002g0212a0001c0002t0002g0213 | 2 | NA19072.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-8-1291T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698197 | ||||||
chr16:50698204
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-8-1284C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698204 | ||||||
chr16:50698205
|
G | A | 4 | a0007c0009t0002g0022a0007c0009t0002g0068a0011c0012t0002g0069others(1): Show | 5 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1283G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698205 | ||||||
chr16:50698222
|
G | A | 25 | a0001c0001t0002g0017a0001c0002t0002g0006a0001c0002t0002g0018others(22): Show | 34 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-8-1266G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698222 | ||||||
chr16:50698346
|
G | A | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8-1142G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698346 | ||||||
chr16:50698395
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8-1093T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698395 | ||||||
chr16:50698511
|
C | T | 6 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-977C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698511 | ||||||
chr16:50698558
|
C | T | 2 | a0004c0007t0002g0110a0004c0007t0002g0111 | 2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-930C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698558 | ||||||
chr16:50698596
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0049others(14): Show | 20 | HG01433.hp2 HG02055.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-892C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698596 | ||||||
chr16:50698615
|
G | A | 5 | a0005c0008t0002g0044a0005c0008t0002g0214a0005c0008t0002g0215others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-873G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698615 | ||||||
chr16:50698792
|
G | C | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-8-696G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698792 | ||||||
chr16:50698878
|
G | A | 3 | a0001c0002t0002g0034a0001c0002t0002g0116a0001c0002t0002g0117 | 4 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-610G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698878 | ||||||
chr16:50698909
|
ATC | A | 6 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-563_-8-562delCT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50698909 | |||||
chr16:50698929
|
C | CT | 26 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0001t0001g0051others(23): Show | 28 | HG00621.hp2 HG01167.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-543dupT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50698929 | |||||
chr16:50698929
|
CT | C | 12 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(9): Show | 12 | HG00733.hp2 HG01081.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-543delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50698929 | |||||
chr16:50699119
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-8-369C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699119 | ||||||
chr16:50699128
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-360G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699128 | ||||||
chr16:50699129
|
T | C | 4 | a0001c0002t0002g0032a0001c0002t0002g0112a0001c0004t0002g0125others(1): Show | 6 | HG02257.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-359T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699129 | ||||||
chr16:50699204
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-8-284C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699204 | ||||||
chr16:50699242
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0170others(9): Show | 15 | HG02074.hp1 HG02080.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-246A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699242 | ||||||
chr16:50699301
|
G | GTGTTTCT | 5 | a0001c0001t0002g0114a0001c0002t0002g0032a0001c0002t0002g0112others(2): Show | 7 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-184_-8-178dupTT others(5): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50699301 | |||||
chr16:50699406
|
G | C | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8-82G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699406 | ||||||
chr16:50699459
|
T | G | 1 | a0002c0005t0001g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-8-29T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699459 | ||||||
chr16:50699463
|
G | T | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0019t0001g0064others(23): Show | 29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-25G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699463 | ||||||
chr16:50700057
|
C | T | 5 | a0005c0008t0002g0044a0005c0008t0002g0214a0005c0008t0002g0215others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+103C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700057 | ||||||
chr16:50700058
|
A | G | 150 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0061others(147): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.459+104A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700058 | ||||||
chr16:50700122
|
G | A | 148 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0061others(145): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.459+168G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700122 | ||||||
chr16:50700224
|
G | A | 6 | a0001c0001t0001g0113a0002c0005t0001g0197a0007c0009t0002g0022others(3): Show | 7 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+270G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700224 | ||||||
chr16:50700289
|
AT | A | 8 | a0001c0001t0001g0164a0001c0003t0001g0008a0001c0003t0001g0023others(5): Show | 12 | HG01106.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+347delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50700289 | |||||
chr16:50700381
|
C | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG02717.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+427C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700381 | ||||||
chr16:50700911
|
G | A | 2 | a0001c0001t0001g0035a0020c0015t0001g0035 | 2 | NA18950.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.459+957G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700911 | ||||||
chr16:50701544
|
G | A | 2 | a0001c0003t0002g0080a0001c0003t0002g0081 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.459+1590G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701544 | ||||||
chr16:50701578
|
G | A | 1 | a0013c0023t0002g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.459+1624G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701578 | ||||||
chr16:50701720
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.459+1766G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701720 | ||||||
chr16:50701857
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.459+1903G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701857 | ||||||
chr16:50701878
|
TA | T | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+1925delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701878 | ||||||
chr16:50702030
|
C | T | 69 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(66): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.459+2076C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702030 | ||||||
chr16:50702050
|
A | T | 1 | a0001c0001t0002g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.459+2096A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702050 | ||||||
chr16:50702255
|
A | G | 1 | a0001c0001t0002g0012 | 3 | HG02257.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.459+2301A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702255 | ||||||
chr16:50702296
|
A | G | 1 | a0001c0004t0002g0102 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.459+2342A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702296 | ||||||
chr16:50702301
|
T | C | 1 | a0002c0005t0001g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.459+2347T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702301 | ||||||
chr16:50702513
|
T | C | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+2559T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702513 | ||||||
chr16:50702745
|
A | G | 102 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(99): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+2791A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702745 | ||||||
chr16:50703366
|
G | A | 1 | a0001c0002t0002g0162 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.459+3412G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703366 | ||||||
chr16:50703531
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.459+3577C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703531 | ||||||
chr16:50703563
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 8 | HG00408.hp1 HG02135.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+3609C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703563 | ||||||
chr16:50703587
|
C | T | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0227others(24): Show | 30 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.459+3633C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703587 | ||||||
chr16:50703638
|
C | T | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.459+3684C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703638 | ||||||
chr16:50703683
|
C | CA | 14 | a0001c0001t0001g0056a0001c0001t0001g0113a0001c0001t0001g0129others(11): Show | 15 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.459+3749dupA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50703683 | |||||
chr16:50703683
|
CA | C | 12 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0187others(9): Show | 15 | HG00323.hp2 HG02257.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.459+3749delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50703683 | |||||
chr16:50703838
|
G | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG03225.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.459+3884G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703838 | ||||||
chr16:50704069
|
A | G | 144 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0062others(141): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.460-3786A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704069 | ||||||
chr16:50704098
|
C | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0006g0050 | 3 | HG02055.hp2 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.460-3757C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704098 | ||||||
chr16:50704332
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0008g0126 | 2 | NA18950.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.460-3523G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704332 | ||||||
chr16:50704380
|
C | T | 2 | a0004c0007t0002g0072a0004c0007t0002g0073 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.460-3475C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704380 | ||||||
chr16:50704532
|
C | CT | 89 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(86): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.460-3310dupT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50704532 | |||||
chr16:50704532
|
CT | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0006g0050others(5): Show | 10 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-3310delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50704532 | |||||
chr16:50704537
|
T | TA | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-3318_460-3317i others(3): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704537 | ||||||
chr16:50704546
|
C | T | 1 | a0001c0002t0002g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.460-3309C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704546 | ||||||
chr16:50704547
|
T | C | 1 | a0001c0002t0002g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.460-3308T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704547 | ||||||
chr16:50704636
|
T | C | 133 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0013others(130): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.460-3219T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704636 | ||||||
chr16:50704746
|
G | T | 2 | a0005c0008t0002g0215a0005c0008t0002g0216 | 2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.460-3109G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704746 | ||||||
chr16:50704883
|
A | G | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.460-2972A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704883 | ||||||
chr16:50704919
|
G | A | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0019t0001g0064others(23): Show | 29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2936G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704919 | ||||||
chr16:50705053
|
T | G | 7 | a0001c0001t0002g0182a0004c0007t0002g0071a0004c0007t0002g0072others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-2802T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705053 | ||||||
chr16:50705194
|
G | A | 134 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0013others(131): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.460-2661G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705194 | ||||||
chr16:50705288
|
CTTTG | C | 5 | a0001c0003t0002g0024a0007c0009t0002g0022a0007c0009t0002g0068others(2): Show | 7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-2554_460-2551d others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50705288 | |||||
chr16:50705350
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.460-2505C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705350 | ||||||
chr16:50705539
|
G | A | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0019t0001g0064others(23): Show | 29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2316G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705539 | ||||||
chr16:50705662
|
C | T | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.460-2193C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705662 | ||||||
chr16:50705671
|
C | G | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0019t0001g0064others(23): Show | 29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2184C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705671 | ||||||
chr16:50705924
|
A | G | 1 | a0001c0003t0002g0081 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.460-1931A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705924 | ||||||
chr16:50705950
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0154others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1905G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705950 | ||||||
chr16:50706056
|
G | A | 1 | a0001c0003t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.460-1799G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706056 | ||||||
chr16:50706263
|
G | C | 16 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(13): Show | 21 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.460-1592G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706263 | ||||||
chr16:50706353
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460-1502G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706353 | ||||||
chr16:50706531
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.460-1324G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706531 | ||||||
chr16:50706698
|
C | CT | 19 | a0001c0001t0001g0160a0001c0001t0002g0013a0001c0001t0002g0017others(16): Show | 24 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.460-1141dupT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50706698 | |||||
chr16:50706698
|
CT | C | 9 | a0001c0001t0004g0058a0001c0001t0008g0126a0001c0004t0002g0087others(6): Show | 9 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-1141delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50706698 | |||||
chr16:50706701
|
T | TC | 4 | a0005c0008t0002g0044a0005c0008t0002g0215a0005c0008t0002g0216others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1154_460-1153i others(3): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706701 | ||||||
chr16:50706720
|
C | T | 3 | a0003c0006t0002g0075a0003c0006t0002g0090a0003c0006t0002g0101 | 3 | HG01081.hp2 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.460-1135C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706720 | ||||||
chr16:50706853
|
C | G | 67 | a0001c0002t0002g0006a0001c0002t0002g0018a0001c0002t0002g0045others(64): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.460-1002C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706853 | ||||||
chr16:50706944
|
C | T | 1 | a0001c0002t0002g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.460-911C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706944 | ||||||
chr16:50706980
|
G | A | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-875G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706980 | ||||||
chr16:50706995
|
G | A | 3 | a0006c0011t0002g0091a0006c0011t0002g0092a0006c0011t0002g0093 | 3 | HG02723.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.460-860G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706995 | ||||||
chr16:50707022
|
T | C | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-833T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707022 | ||||||
chr16:50707078
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-777A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707078 | ||||||
chr16:50707233
|
G | C | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-622G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707233 | ||||||
chr16:50707275
|
C | A | 70 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060others(67): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.460-580C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707275 | ||||||
chr16:50707551
|
A | C | 67 | a0001c0002t0002g0006a0001c0002t0002g0018a0001c0002t0002g0045others(64): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.460-304A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707551 | ||||||
chr16:50707772
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.460-83A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707772 | ||||||
chr16:50707852
|
T | C | 4 | a0001c0002t0002g0034a0001c0002t0002g0116a0001c0002t0002g0117others(1): Show | 5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.460-3T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707852 | ||||||
chr16:50708150
|
C | T | 1 | a0005c0008t0002g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565+190C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708150 | ||||||
chr16:50708151
|
G | A | 10 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(7): Show | 15 | HG00639.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+191G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708151 | ||||||
chr16:50708461
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.565+501G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708461 | ||||||
chr16:50708579
|
A | T | 3 | a0001c0004t0002g0105a0001c0004t0002g0106a0001c0004t0002g0125 | 3 | HG02258.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.565+619A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708579 | ||||||
chr16:50708770
|
G | A | 32 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0227others(29): Show | 37 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+810G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708770 | ||||||
chr16:50708804
|
C | T | 1 | a0001c0003t0002g0029 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.565+844C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708804 | ||||||
chr16:50708860
|
C | A | 1 | a0001c0002t0002g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+900C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708860 | ||||||
chr16:50709025
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+1065G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709025 | ||||||
chr16:50709027
|
G | A | 32 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0227others(29): Show | 37 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+1067G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709027 | ||||||
chr16:50709419
|
C | T | 1 | a0004c0007t0002g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.566-1139C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709419 | ||||||
chr16:50709420
|
G | A | 66 | a0001c0002t0002g0006a0001c0002t0002g0018a0001c0002t0002g0045others(63): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.566-1138G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709420 | ||||||
chr16:50709636
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.566-922G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709636 | ||||||
chr16:50709665
|
C | T | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-893C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709665 | ||||||
chr16:50710008
|
C | T | 66 | a0001c0002t0002g0006a0001c0002t0002g0018a0001c0002t0002g0045others(63): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.566-550C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710008 | ||||||
chr16:50710123
|
C | T | 2 | a0007c0009t0002g0022a0007c0009t0002g0068 | 3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.566-435C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710123 | ||||||
chr16:50710163
|
C | T | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 25 | HG01433.hp2 HG02055.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-395C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710163 | ||||||
chr16:50710188
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566-370G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710188 | ||||||
chr16:50710226
|
G | T | 3 | a0001c0002t0002g0032a0001c0002t0002g0112a0009c0014t0002g0033 | 5 | HG02257.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-332G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710226 | ||||||
chr16:50710481
|
C | T | 1 | a0001c0004t0002g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.566-77C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710481 | ||||||
chr16:50712383
|
A | C | 1 | a0001c0004t0002g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2381+10A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712383 | ||||||
chr16:50712440
|
C | T | 1 | a0004c0007t0002g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2381+67C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712440 | ||||||
chr16:50712635
|
C | G | 130 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(127): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2381+262C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712635 | ||||||
chr16:50712874
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2381+501A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712874 | ||||||
chr16:50712903
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0149others(3): Show | 8 | HG01071.hp1 HG01928.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2381+530C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712903 | ||||||
chr16:50713190
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2381+817G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713190 | ||||||
chr16:50713277
|
C | T | 2 | a0001c0001t0001g0147a0004c0007t0002g0071 | 2 | HG01891.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2381+904C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713277 | ||||||
chr16:50713280
|
C | G | 5 | a0001c0003t0002g0024a0007c0009t0002g0022a0007c0009t0002g0068others(2): Show | 7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2381+907C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713280 | ||||||
chr16:50713504
|
C | G | 5 | a0001c0003t0002g0024a0007c0009t0002g0022a0007c0009t0002g0068others(2): Show | 7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2381+1131C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713504 | ||||||
chr16:50713698
|
G | A | 1 | a0001c0001t0010g0156 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2381+1325G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713698 | ||||||
chr16:50713793
|
C | T | 31 | a0001c0001t0001g0010a0001c0003t0002g0024a0001c0019t0001g0064others(28): Show | 38 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.2381+1420C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713793 | ||||||
chr16:50713828
|
C | G | 26 | a0001c0001t0001g0010a0001c0019t0001g0064a0002c0005t0001g0004others(23): Show | 31 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.2381+1455C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713828 | ||||||
chr16:50713833
|
C | T | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2381+1460C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713833 | ||||||
chr16:50713924
|
C | T | 1 | a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2381+1551C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713924 | ||||||
chr16:50713963
|
G | A | 16 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(13): Show | 21 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2381+1590G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713963 | ||||||
chr16:50714242
|
C | G | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2381+1869C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714242 | ||||||
chr16:50714329
|
C | T | 1 | a0004c0007t0002g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2381+1956C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714329 | ||||||
chr16:50714330
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2381+1957G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714330 | ||||||
chr16:50714404
|
A | G | 2 | a0001c0003t0001g0076a0001c0003t0001g0079 | 2 | HG01106.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2381+2031A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714404 | ||||||
chr16:50714437
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2381+2064A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714437 | ||||||
chr16:50714515
|
C | T | 1 | a0007c0009t0002g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2382-2072C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714515 | ||||||
chr16:50714593
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2382-1994G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714593 | ||||||
chr16:50714602
|
C | CTG | 39 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0123others(36): Show | 49 | HG00140.hp2 HG01167.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.2382-1945_2382-194 others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | |||||
chr16:50714602
|
C | CTGTG | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0113others(16): Show | 27 | HG00280.hp2 HG01175.hp2 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.2382-1947_2382-194 others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | |||||
chr16:50714602
|
CTG | C | 38 | a0001c0001t0001g0036a0001c0001t0001g0129a0001c0001t0001g0135others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.2382-1945_2382-194 others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | |||||
chr16:50714602
|
CTGTG | C | 22 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0049others(19): Show | 29 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.2382-1947_2382-194 others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | |||||
chr16:50714602
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2382-1957_2382-194 others(18): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | |||||
chr16:50714602
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2382-1961_2382-194 others(22): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | |||||
chr16:50714647
|
A | T | 1 | a0011c0012t0002g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2382-1940A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714647 | ||||||
chr16:50714710
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG02074.hp1 HG02083.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2382-1877C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714710 | ||||||
chr16:50714789
|
A | G | 1 | a0002c0005t0001g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2382-1798A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714789 | ||||||
chr16:50714892
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2382-1695G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714892 | ||||||
chr16:50714944
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2382-1643T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714944 | ||||||
chr16:50715156
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2382-1431T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715156 | ||||||
chr16:50715255
|
AT | A | 5 | a0001c0003t0002g0024a0007c0009t0002g0022a0007c0009t0002g0068others(2): Show | 7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2382-1329delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50715255 | |||||
chr16:50715420
|
CT | C | 68 | a0001c0001t0002g0012a0001c0001t0002g0114a0001c0001t0002g0227others(65): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2382-1154delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50715420 | |||||
chr16:50715420
|
CTT | C | 16 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(13): Show | 21 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2382-1155_2382-115 others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50715420 | |||||
chr16:50715460
|
G | C | 3 | a0001c0004t0002g0105a0001c0004t0002g0106a0001c0004t0002g0125 | 3 | HG02258.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2382-1127G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715460 | ||||||
chr16:50715463
|
A | T | 130 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(127): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2382-1124A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715463 | ||||||
chr16:50715497
|
G | T | 25 | a0001c0019t0001g0064a0002c0005t0001g0004a0002c0005t0001g0007others(22): Show | 28 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2382-1090G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715497 | ||||||
chr16:50715576
|
C | T | 1 | a0001c0025t0001g0202 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2382-1011C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715576 | ||||||
chr16:50715598
|
G | C | 5 | a0005c0008t0002g0044a0005c0008t0002g0214a0005c0008t0002g0215others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2382-989G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715598 | ||||||
chr16:50715763
|
G | A | 1 | a0001c0004t0002g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2382-824G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715763 | ||||||
chr16:50715765
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2382-822T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715765 | ||||||
chr16:50716132
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2382-455G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716132 | ||||||
chr16:50716191
|
G | A | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2382-396G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716191 | ||||||
chr16:50716224
|
G | A | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2382-363G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716224 | ||||||
chr16:50716258
|
T | G | 1 | a0001c0003t0002g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2382-329T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716258 | ||||||
chr16:50716784
|
G | C | 1 | a0001c0004t0002g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2466-107G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 5/11 | chr16 | 50716784 | ||||||
chr16:50716849
|
T | C | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2466-42T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 5/11 | chr16 | 50716849 | ||||||
chr16:50716880
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2466-11G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 5/11 | chr16 | 50716880 | ||||||
chr16:50717030
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0143 | 2 | NA18943.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2549+56C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717030 | ||||||
chr16:50717076
|
C | T | 2 | a0004c0007t0002g0072a0004c0007t0002g0073 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2549+102C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717076 | ||||||
chr16:50717264
|
T | G | 133 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(130): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2549+290T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717264 | ||||||
chr16:50717487
|
A | G | 68 | a0001c0001t0002g0012a0001c0001t0005g0104a0001c0002t0002g0006others(65): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2549+513A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717487 | ||||||
chr16:50717650
|
C | T | 1 | a0001c0001t0001g0041 | 2 | HG02145.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2549+676C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717650 | ||||||
chr16:50717651
|
G | T | 1 | a0001c0003t0003g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2549+677G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717651 | ||||||
chr16:50717810
|
C | T | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2549+836C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717810 | ||||||
chr16:50717876
|
G | A | 68 | a0001c0001t0002g0012a0001c0001t0002g0227a0001c0002t0002g0006others(65): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2549+902G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717876 | ||||||
chr16:50718061
|
G | A | 125 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(122): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.2549+1087G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718061 | ||||||
chr16:50718179
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2549+1205G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718179 | ||||||
chr16:50718198
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2549+1224C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718198 | ||||||
chr16:50718253
|
G | A | 20 | a0001c0019t0001g0064a0002c0005t0001g0004a0002c0005t0001g0007others(17): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2549+1279G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718253 | ||||||
chr16:50718373
|
G | A | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2549+1399G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718373 | ||||||
chr16:50718533
|
C | A | 15 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(12): Show | 20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2550-1392C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718533 | ||||||
chr16:50718636
|
C | T | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2550-1289C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718636 | ||||||
chr16:50718671
|
C | T | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2550-1254C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718671 | ||||||
chr16:50718794
|
G | A | 1 | a0007c0009t0002g0022 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2550-1131G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718794 | ||||||
chr16:50718904
|
T | C | 56 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(53): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.2550-1021T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718904 | ||||||
chr16:50719116
|
C | T | 1 | a0005c0008t0002g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2550-809C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719116 | ||||||
chr16:50719224
|
C | T | 1 | a0001c0019t0001g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2550-701C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719224 | ||||||
chr16:50719513
|
G | A | 68 | a0001c0001t0002g0012a0001c0001t0002g0227a0001c0002t0002g0006others(65): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.2550-412G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719513 | ||||||
chr16:50719514
|
C | G | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2550-411C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719514 | ||||||
chr16:50719639
|
C | T | 15 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(12): Show | 20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2550-286C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719639 | ||||||
chr16:50719730
|
C | G | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2550-195C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719730 | ||||||
chr16:50720114
|
G | A | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2633+106G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720114 | ||||||
chr16:50720242
|
G | C | 5 | a0005c0008t0002g0044a0005c0008t0002g0214a0005c0008t0002g0215others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2633+234G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720242 | ||||||
chr16:50720279
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2633+271G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720279 | ||||||
chr16:50720479
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | NA18947.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2633+471A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720479 | ||||||
chr16:50720996
|
G | A | 3 | a0003c0006t0002g0075a0003c0006t0002g0090a0003c0006t0002g0101 | 3 | HG01081.hp2 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2633+988G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720996 | ||||||
chr16:50721014
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2633+1006C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721014 | ||||||
chr16:50721277
|
ATATT | A | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2633+1274_2633+127 others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 50721277 | |||||
chr16:50721307
|
C | T | 4 | a0001c0002t0002g0034a0001c0002t0002g0116a0001c0002t0002g0117others(1): Show | 5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2633+1299C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721307 | ||||||
chr16:50721366
|
GT | G | 106 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(103): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.2634-1245delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 50721366 | |||||
chr16:50721374
|
T | G | 1 | a0001c0001t0008g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2634-1248T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721374 | ||||||
chr16:50721377
|
TG | T | 9 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0177others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634-1244delG | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721377 | ||||||
chr16:50721378
|
G | T | 10 | a0001c0001t0001g0049a0001c0001t0001g0170a0001c0001t0001g0171others(7): Show | 10 | HG01433.hp2 HG02080.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2634-1244G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721378 | ||||||
chr16:50721626
|
G | T | 1 | a0007c0009t0002g0022 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2634-996G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721626 | ||||||
chr16:50721643
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2634-979C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721643 | ||||||
chr16:50721798
|
T | G | 67 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(64): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2634-824T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721798 | ||||||
chr16:50721818
|
G | A | 3 | a0001c0003t0002g0024a0011c0012t0002g0069a0011c0012t0002g0070 | 4 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2634-804G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721818 | ||||||
chr16:50721837
|
T | C | 4 | a0001c0002t0002g0034a0001c0002t0002g0116a0001c0002t0002g0117others(1): Show | 5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634-785T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721837 | ||||||
chr16:50721840
|
C | T | 1 | a0001c0002t0002g0225 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2634-782C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721840 | ||||||
chr16:50721894
|
G | A | 10 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(7): Show | 15 | HG00639.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2634-728G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721894 | ||||||
chr16:50722009
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2634-613G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722009 | ||||||
chr16:50722156
|
C | T | 1 | a0001c0001t0004g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2634-466C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722156 | ||||||
chr16:50722364
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2634-258G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722364 | ||||||
chr16:50722387
|
C | G | 17 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(14): Show | 22 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2634-235C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722387 | ||||||
chr16:50722500
|
T | G | 2 | a0001c0001t0004g0059a0001c0001t0004g0060 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2634-122T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722500 | ||||||
chr16:50722805
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2717+100C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50722805 | ||||||
chr16:50722863
|
C | T | 11 | a0001c0001t0001g0161a0002c0005t0001g0004a0002c0005t0001g0019others(8): Show | 13 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2717+158C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50722863 | ||||||
chr16:50722970
|
A | G | 20 | a0001c0019t0001g0064a0002c0005t0001g0004a0002c0005t0001g0007others(17): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2717+265A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50722970 | ||||||
chr16:50723085
|
T | TA | 17 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(14): Show | 22 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2718-200dupA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723085 | |||||
chr16:50723085
|
TA | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(162): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2718-200delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723085 | |||||
chr16:50723139
|
G | GA | 79 | a0001c0001t0001g0009a0001c0001t0001g0146a0001c0001t0001g0150others(76): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2718-147dupA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723139 | |||||
chr16:50723139
|
GA | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0047others(7): Show | 14 | HG00621.hp2 HG01071.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2718-147delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723139 | |||||
chr16:50723139
|
GAAAAAA | G | 6 | a0004c0007t0002g0071a0004c0007t0002g0072a0004c0007t0002g0073others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2718-152_2718-147d others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723139 | |||||
chr16:50723277
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2718-24C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50723277 | ||||||
chr16:50723573
|
C | T | 1 | a0001c0004t0002g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2801+189C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723573 | ||||||
chr16:50723631
|
G | A | 2 | a0001c0003t0001g0076a0001c0003t0001g0079 | 2 | HG01106.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2801+247G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723631 | ||||||
chr16:50723692
|
A | G | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2801+308A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723692 | ||||||
chr16:50723734
|
G | A | 4 | a0001c0002t0002g0046a0001c0002t0002g0221a0001c0002t0002g0223others(1): Show | 5 | HG02132.hp2 NA18940.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2801+350G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723734 | ||||||
chr16:50723969
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0002g0227 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2801+585T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723969 | ||||||
chr16:50724241
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2801+857A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724241 | ||||||
chr16:50724593
|
T | C | 7 | a0001c0001t0002g0182a0004c0007t0002g0071a0004c0007t0002g0072others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2802-896T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724593 | ||||||
chr16:50724758
|
T | A | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2802-731T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724758 | ||||||
chr16:50724927
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(232): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2802-562T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724927 | ||||||
chr16:50724938
|
G | A | 20 | a0001c0019t0001g0064a0002c0005t0001g0004a0002c0005t0001g0007others(17): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2802-551G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724938 | ||||||
chr16:50725100
|
T | C | 1 | a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2802-389T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725100 | ||||||
chr16:50725230
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2802-259A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725230 | ||||||
chr16:50725356
|
AC | A | 66 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(63): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.2802-132delC | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725356 | ||||||
chr16:50725358
|
T | A | 66 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(63): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.2802-131T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725358 | ||||||
chr16:50725636
|
A | T | 86 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(83): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.2885+64A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50725636 | ||||||
chr16:50725820
|
T | A | 1 | a0010c0013t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2885+248T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50725820 | ||||||
chr16:50726069
|
A | C | 127 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(124): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2885+497A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726069 | ||||||
chr16:50726100
|
G | A | 2 | a0001c0001t0002g0114a0001c0001t0002g0227 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2885+528G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726100 | ||||||
chr16:50726127
|
C | T | 3 | a0003c0006t0002g0075a0003c0006t0002g0090a0003c0006t0002g0101 | 3 | HG01081.hp2 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2885+555C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726127 | ||||||
chr16:50726208
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0141 | 2 | HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2885+636C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726208 | ||||||
chr16:50726217
|
G | A | 1 | a0001c0001t0004g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2885+645G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726217 | ||||||
chr16:50726245
|
G | GCCAAAAT others(307): Show |
7 | a0001c0001t0002g0182a0004c0007t0002g0071a0004c0007t0002g0072others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2885+684_2885+685i others(316): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 50726245 | |||||
chr16:50726352
|
C | A | 7 | a0001c0001t0001g0154a0001c0001t0001g0177a0001c0001t0001g0179others(4): Show | 7 | HG01167.hp2 HG02055.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2885+780C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726352 | ||||||
chr16:50726360
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2885+788G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726360 | ||||||
chr16:50726425
|
C | T | 1 | a0001c0003t0002g0029 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2885+853C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726425 | ||||||
chr16:50726453
|
C | T | 3 | a0001c0003t0002g0024a0011c0012t0002g0069a0011c0012t0002g0070 | 4 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2885+881C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726453 | ||||||
chr16:50726492
|
A | T | 7 | a0001c0001t0001g0154a0001c0001t0001g0177a0001c0001t0001g0179others(4): Show | 7 | HG01167.hp2 HG02055.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2885+920A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726492 | ||||||
chr16:50726534
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2885+962C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726534 | ||||||
chr16:50726777
|
T | C | 7 | a0001c0001t0002g0182a0004c0007t0002g0071a0004c0007t0002g0072others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2885+1205T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726777 | ||||||
chr16:50726916
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2885+1344G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726916 | ||||||
chr16:50726927
|
A | G | 127 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0017others(124): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2885+1355A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726927 | ||||||
chr16:50727138
|
CA | C | 43 | a0001c0001t0001g0119a0001c0001t0002g0013a0001c0001t0002g0017others(40): Show | 52 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2885+1583delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 50727138 | |||||
chr16:50727177
|
A | T | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(15): Show | 24 | HG01433.hp2 HG02055.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2885+1605A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727177 | ||||||
chr16:50727507
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2885+1935A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727507 | ||||||
chr16:50727523
|
C | T | 66 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(63): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.2885+1951C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727523 | ||||||
chr16:50727532
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2885+1960A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727532 | ||||||
chr16:50727659
|
G | A | 15 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(12): Show | 20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2885+2087G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727659 | ||||||
chr16:50727669
|
A | ATAGTCCA others(14): Show |
1 | a0001c0001t0007g0140 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2885+2099_2885+211 others(25): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 50727669 | |||||
chr16:50727729
|
G | A | 1 | a0001c0004t0002g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2886-2089G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727729 | ||||||
chr16:50727729
|
G | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0227 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2886-2089G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727729 | ||||||
chr16:50727755
|
C | T | 1 | a0001c0025t0001g0202 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2886-2063C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727755 | ||||||
chr16:50727799
|
A | T | 3 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2886-2019A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727799 | ||||||
chr16:50728058
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 5 | NA18947.hp1 NA18986.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2886-1760C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728058 | ||||||
chr16:50728075
|
T | A | 1 | a0001c0027t0002g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2886-1743T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728075 | ||||||
chr16:50728126
|
C | T | 15 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(12): Show | 20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2886-1692C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728126 | ||||||
chr16:50728214
|
T | A | 5 | a0005c0008t0002g0044a0005c0008t0002g0214a0005c0008t0002g0215others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2886-1604T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728214 | ||||||
chr16:50728222
|
A | G | 7 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0112others(4): Show | 10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2886-1596A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728222 | ||||||
chr16:50728623
|
T | G | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2886-1195T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728623 | ||||||
chr16:50728647
|
C | A | 1 | a0017c0028t0001g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2886-1171C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728647 | ||||||
chr16:50728673
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2886-1145T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728673 | ||||||
chr16:50728860
|
T | C | 2 | a0001c0004t0002g0085a0001c0004t0002g0098 | 2 | HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2886-958T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728860 | ||||||
chr16:50729165
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2886-653G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50729165 | ||||||
chr16:50729285
|
A | G | 5 | a0005c0008t0002g0044a0005c0008t0002g0214a0005c0008t0002g0215others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2886-533A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50729285 | ||||||
chr16:50729398
|
C | G | 1 | a0007c0009t0002g0022 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2886-420C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50729398 | ||||||
chr16:50730205
|
G | A | 25 | a0001c0001t0001g0142a0001c0001t0002g0013a0001c0001t0002g0017others(22): Show | 30 | HG00639.hp2 HG01891.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.2969+304G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730205 | ||||||
chr16:50730315
|
A | G | 15 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(12): Show | 20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2969+414A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730315 | ||||||
chr16:50730488
|
C | T | 24 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(21): Show | 29 | HG00639.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2969+587C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730488 | ||||||
chr16:50730876
|
C | T | 1 | a0001c0004t0002g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2970-871C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730876 | ||||||
chr16:50730923
|
G | A | 2 | a0001c0001t0002g0114a0001c0001t0002g0227 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2970-824G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730923 | ||||||
chr16:50730925
|
G | A | 64 | a0001c0001t0002g0012a0001c0002t0002g0006a0001c0002t0002g0018others(61): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.2970-822G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730925 | ||||||
chr16:50731042
|
C | T | 4 | a0001c0002t0002g0034a0001c0002t0002g0116a0001c0002t0002g0117others(1): Show | 5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2970-705C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731042 | ||||||
chr16:50731077
|
G | A | 18 | a0001c0002t0002g0006a0001c0002t0002g0018a0001c0002t0002g0045others(15): Show | 25 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.2970-670G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731077 | ||||||
chr16:50731140
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2970-607C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731140 | ||||||
chr16:50731308
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2970-439A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731308 | ||||||
chr16:50731465
|
A | G | 39 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0040others(36): Show | 49 | HG00639.hp2 HG01884.hp1 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.2970-282A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731465 | ||||||
chr16:50731599
|
C | T | 1 | a0001c0002t0002g0213 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2970-148C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731599 | ||||||
chr16:50731614
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 5 | NA18947.hp1 NA18986.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2970-133T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731614 |