geneid | 221184 |
---|---|
ensemblid | ENSG00000140848.17 |
hgncid | 2315 |
symbol | CPNE2 |
name | copine 2 |
refseq_nuc | NM_152727.6 |
refseq_prot | NP_689940.3 |
ensembl_nuc | ENST00000290776.13 |
ensembl_prot | ENSP00000290776.8 |
mane_status | MANE Select |
chr | chr16 |
start | 57092583 |
end | 57148369 |
strand | + |
ver | v1.2 |
region | chr16:57092583-57148369 |
region5000 | chr16:57087583-57153369 |
regionname0 | CPNE2_chr16_57092583_57148369 |
regionname5000 | CPNE2_chr16_57087583_57153369 |
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 | 548 | 358 | 91 | 58 | 151 | 14 | 42 | 117 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0002 | 0/0 | 548 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0003 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
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 | 1647 | 308 | 83 | 57 | 120 | 14 | 33 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0002 | 0/0 | 1647 | 38 | 0 | 1 | 28 | 0 | 9 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0003 | 0/1 | 1647 | 4 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0004 | 0/0 | 1647 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0005 | 0/0 | 1647 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0006 | 0/0 | 1647 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0007 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
c0008 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
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 | 1/0 | 955 | 336 | 81 | 57 | 146 | 12 | 39 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0002 | 0/0 | 955 | 11 | 10 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0003 | 0/1 | 955 | 7 | 2 | 1 | 0 | 2 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0004 | 0/0 | 956 | 4 | 0 | 0 | 4 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0005 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0006 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0007 | 0/0 | 955 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
t0008 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
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 | 1647 | 308 | 83 | 57 | 120 | 14 | 33 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0002 | 0/0 | 1647 | 38 | 0 | 1 | 28 | 0 | 9 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0003 | 0/1 | 1647 | 4 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0005 | 0/0 | 1647 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0006 | 0/0 | 1647 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0007 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0002c0004 | 0/0 | 1647 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0003c0008 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2601 | 286 | 70 | 56 | 117 | 12 | 30 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0002 | 0/0 | 2601 | 11 | 10 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0003 | 0/0 | 2601 | 6 | 2 | 1 | 0 | 2 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0004 | 0/0 | 2602 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0005 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0006 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0007 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0001t0008 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0002t0001 | 0/0 | 2601 | 35 | 0 | 1 | 25 | 0 | 9 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0002t0004 | 0/0 | 2602 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0003t0001 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0003t0003 | 0/1 | 2601 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0005t0001 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0006t0001 | 0/0 | 2601 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0001c0007t0001 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0002c0004t0001 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
a0003c0008t0001 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | copy fasta | chr16 | 57087583 | 57153369 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0003t0003g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0005t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0001c0007t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0002c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0002c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
a0003c0008t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0306 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0164 | EUR | IBS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02572 | hp1 | a0001 | c0007 | t0001 | g0302 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02622 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0294 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0309 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02717 | hp2 | a0002 | c0004 | t0001 | g0162 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0097 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02886 | hp2 | a0001 | c0007 | t0001 | g0090 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0333 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0332 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18942 | hp1 | a0001 | c0002 | t0004 | g0173 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18961 | hp1 | a0003 | c0008 | t0001 | g0056 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18965 | hp2 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18998 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19000 | hp1 | a0001 | c0006 | t0001 | g0190 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19043 | hp2 | a0002 | c0004 | t0001 | g0039 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19060 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19062 | hp2 | a0001 | c0006 | t0001 | g0184 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19083 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ASW | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | GIH | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
HG06807 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0003 | g0276 | REF | REF | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0283 | REF | REF | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57110901
|
G | C | 1 | a0002 | 3 | HG02622.hp1 HG02717.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.159G>C | p.Glu53Asp | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/16 | 402/2601 | 159/1647 | 53/548 | chr16 | 57110901 | ||
chr16:57119209
|
G | T | 1 | a0003 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.522G>T | p.Lys174Asn | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 6/16 | 765/2601 | 522/1647 | 174/548 | chr16 | 57119209 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57113362
|
C | T | 1 | a0001c0003 | 4 | HG02886.hp1 HG03540.hp1 NA19030.hp1 others(1): Show |
synonymous_variant | LOW | c.255C>T | p.Phe85Phe | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/16 | 498/2601 | 255/1647 | 85/548 | chr16 | 57113362 | ||
chr16:57117546
|
G | A | 1 | a0001c0007 | 2 | HG02572.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.486G>A | p.Ala162Ala | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/16 | 729/2601 | 486/1647 | 162/548 | chr16 | 57117546 | ||
chr16:57146165
|
C | A | 1 | a0001c0005 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1383C>A | p.Ser461Ser | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/16 | 1626/2601 | 1383/1647 | 461/548 | chr16 | 57146165 | ||
chr16:57146246
|
C | A | 1 | a0001c0002 | 38 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(35): Show |
synonymous_variant | LOW | c.1464C>A | p.Arg488Arg | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/16 | 1707/2601 | 1464/1647 | 488/548 | chr16 | 57146246 | ||
chr16:57146288
|
T | C | 1 | a0001c0006 | 3 | NA18965.hp2 NA19000.hp1 NA19062.hp2 |
synonymous_variant | LOW | c.1506T>C | p.Ile502Ile | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/16 | 1749/2601 | 1506/1647 | 502/548 | chr16 | 57146288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57092592
|
C | G | 1 | a0001c0001t0008 | 1 | NA19060.hp1 | 5_prime_UTR_variant | MODIFIER | c.-234C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/16 | 18151 | chr16 | 57092592 | |||||
chr16:57110736
|
G | A | 1 | a0001c0001t0005 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/16 | 7 | chr16 | 57110736 | |||||
chr16:57147771
|
T | A | 1 | a0001c0001t0006 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 113 | chr16 | 57147771 | |||||
chr16:57147964
|
T | C | 2 | a0001c0001t0003a0001c0003t0003 | 7 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*306T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 306 | chr16 | 57147964 | |||||
chr16:57147970
|
G | A | 1 | a0001c0001t0007 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 312 | chr16 | 57147970 | |||||
chr16:57148026
|
T | TA | 2 | a0001c0001t0004a0001c0002t0004 | 4 | NA18942.hp1 NA18970.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*369dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 370 | INFO_REALIGN_3_PRIME | chr16 | 57148026 | ||||
chr16:57148265
|
T | C | 1 | a0001c0001t0002 | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*607T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 607 | chr16 | 57148265 | |||||
chr16:57148356
|
A | G | 2 | a0001c0001t0003a0001c0003t0003 | 7 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*698A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 698 | chr16 | 57148356 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57093349
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36+559T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093349 | ||||||
chr16:57093441
|
C | G | 1 | a0001c0001t0001g0342 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-36+651C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093441 | ||||||
chr16:57093453
|
C | A | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(18): Show | 22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36+663C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093453 | ||||||
chr16:57093522
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG01243.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-36+732C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093522 | ||||||
chr16:57093538
|
G | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-36+748G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093538 | ||||||
chr16:57093596
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0334others(5): Show | 10 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36+806C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093596 | ||||||
chr16:57093723
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+933C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093723 | ||||||
chr16:57093800
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0005g0038 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-36+1010C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093800 | ||||||
chr16:57093841
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-36+1051G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093841 | ||||||
chr16:57093895
|
G | A | 1 | a0001c0007t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36+1105G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093895 | ||||||
chr16:57093971
|
C | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-36+1181C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093971 | ||||||
chr16:57094095
|
AGCTCCAG others(4): Show |
A | 2 | a0002c0004t0001g0039a0002c0004t0001g0040 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-36+1308_-36+1318d others(13): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57094095 | |||||
chr16:57094184
|
G | A | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+1394G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094184 | ||||||
chr16:57094187
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 119 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-36+1397T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094187 | ||||||
chr16:57094220
|
C | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-36+1430C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094220 | ||||||
chr16:57094400
|
C | T | 1 | a0001c0001t0007g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36+1610C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094400 | ||||||
chr16:57094443
|
A | T | 2 | a0001c0002t0001g0198a0001c0006t0001g0199 | 2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-36+1653A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094443 | ||||||
chr16:57094476
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-36+1686G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094476 | ||||||
chr16:57094478
|
T | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+1688T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094478 | ||||||
chr16:57094489
|
G | A | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-36+1699G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094489 | ||||||
chr16:57094529
|
A | G | 2 | a0001c0003t0001g0014a0001c0003t0001g0333 | 3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-36+1739A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094529 | ||||||
chr16:57094543
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+1753A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094543 | ||||||
chr16:57094579
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-36+1789T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094579 | ||||||
chr16:57094833
|
G | A | 19 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.-36+2043G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094833 | ||||||
chr16:57094959
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 53 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-36+2169G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094959 | ||||||
chr16:57094968
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-36+2178G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094968 | ||||||
chr16:57094971
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA19060.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-36+2181C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094971 | ||||||
chr16:57094974
|
G | A | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+2184G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094974 | ||||||
chr16:57094976
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-36+2186T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094976 | ||||||
chr16:57095072
|
G | C | 3 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0003g0220 | 3 | HG03688.hp1 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-36+2282G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095072 | ||||||
chr16:57095178
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-36+2388C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095178 | ||||||
chr16:57095619
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-36+2829C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095619 | ||||||
chr16:57095653
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0324a0001c0001t0001g0325others(5): Show | 10 | NA18944.hp2 NA18952.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36+2863C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095653 | ||||||
chr16:57095712
|
A | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 108 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-36+2922A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095712 | ||||||
chr16:57095745
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-36+2955A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095745 | ||||||
chr16:57095768
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-36+2978G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095768 | ||||||
chr16:57096042
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-36+3252T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096042 | ||||||
chr16:57096105
|
G | GTTTAAAT others(4): Show |
1 | a0001c0001t0001g0083 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-36+3317_-36+3318i others(13): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57096105 | |||||
chr16:57096119
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-36+3329T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096119 | ||||||
chr16:57096549
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-36+3759A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096549 | ||||||
chr16:57096573
|
C | T | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 8 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-36+3783C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096573 | ||||||
chr16:57096698
|
C | CA | 67 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(64): Show | 70 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.-36+3927dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57096698 | |||||
chr16:57096698
|
CA | C | 15 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(12): Show | 15 | HG00673.hp2 HG02015.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-36+3927delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57096698 | |||||
chr16:57096725
|
G | T | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-36+3935G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096725 | ||||||
chr16:57097087
|
C | G | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36+4297C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097087 | ||||||
chr16:57097121
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | HG01433.hp1 HG01496.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+4331G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097121 | ||||||
chr16:57097169
|
A | T | 1 | a0001c0001t0006g0315 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-36+4379A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097169 | ||||||
chr16:57097285
|
A | T | 1 | a0001c0001t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-36+4495A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097285 | ||||||
chr16:57097388
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.-36+4598A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097388 | ||||||
chr16:57097416
|
A | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+4626A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097416 | ||||||
chr16:57097490
|
G | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0100others(51): Show | 55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+4700G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097490 | ||||||
chr16:57097622
|
T | C | 38 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0168others(35): Show | 39 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36+4832T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097622 | ||||||
chr16:57097865
|
C | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0100others(51): Show | 55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+5075C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097865 | ||||||
chr16:57097917
|
C | T | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+5127C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097917 | ||||||
chr16:57097958
|
G | C | 2 | a0001c0003t0001g0014a0001c0003t0001g0333 | 3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-36+5168G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097958 | ||||||
chr16:57098032
|
C | T | 1 | a0001c0007t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36+5242C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098032 | ||||||
chr16:57098034
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+5244A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098034 | ||||||
chr16:57098151
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+5361G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098151 | ||||||
chr16:57098273
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-36+5483C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098273 | ||||||
chr16:57098277
|
G | A | 50 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(47): Show | 51 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(48): Show |
intron_variant | MODIFIER | c.-36+5487G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098277 | ||||||
chr16:57098333
|
C | T | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+5543C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098333 | ||||||
chr16:57098342
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0100others(51): Show | 55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+5552G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098342 | ||||||
chr16:57098351
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.-36+5561A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098351 | ||||||
chr16:57098406
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | NA18946.hp1 NA19062.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-36+5616G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098406 | ||||||
chr16:57098419
|
C | T | 1 | a0001c0001t0007g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36+5629C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098419 | ||||||
chr16:57098452
|
C | T | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+5662C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098452 | ||||||
chr16:57098668
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-36+5878C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098668 | ||||||
chr16:57098785
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-36+5995C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098785 | ||||||
chr16:57098873
|
G | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-36+6083G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098873 | ||||||
chr16:57098937
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36+6147T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098937 | ||||||
chr16:57099092
|
C | A | 48 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0085others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36+6302C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099092 | ||||||
chr16:57099157
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.-36+6367A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099157 | ||||||
chr16:57099261
|
C | T | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(18): Show | 22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36+6471C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099261 | ||||||
chr16:57099291
|
A | G | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+6501A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099291 | ||||||
chr16:57099349
|
A | G | 38 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0168others(35): Show | 39 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36+6559A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099349 | ||||||
chr16:57099439
|
C | T | 38 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0168others(35): Show | 39 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36+6649C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099439 | ||||||
chr16:57099459
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-36+6669A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099459 | ||||||
chr16:57099607
|
C | CT | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+6827dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099607 | |||||
chr16:57099660
|
C | T | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+6870C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099660 | ||||||
chr16:57099748
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 170 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-36+6958T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099748 | ||||||
chr16:57099775
|
A | AT | 43 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0018others(40): Show | 45 | HG00140.hp1 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-36+7006dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099775 | |||||
chr16:57099775
|
AT | A | 19 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0047others(16): Show | 20 | HG01069.hp1 HG01884.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-36+7006delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099775 | |||||
chr16:57099775
|
ATT | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+7005_-36+7006d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099775 | |||||
chr16:57099838
|
C | T | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-36+7048C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099838 | ||||||
chr16:57099971
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-36+7181C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099971 | ||||||
chr16:57099995
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0107others(22): Show | 26 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-36+7205G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099995 | ||||||
chr16:57100024
|
C | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0100others(51): Show | 55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+7234C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100024 | ||||||
chr16:57100372
|
A | G | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-36+7582A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100372 | ||||||
chr16:57100426
|
A | G | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+7636A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100426 | ||||||
chr16:57100526
|
A | G | 2 | a0001c0003t0001g0014a0001c0003t0001g0333 | 3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-36+7736A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100526 | ||||||
chr16:57100822
|
G | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8032G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100822 | ||||||
chr16:57100826
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36+8036G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100826 | ||||||
chr16:57100922
|
AT | A | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(18): Show | 22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36+8134delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57100922 | |||||
chr16:57101009
|
G | A | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8219G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101009 | ||||||
chr16:57101065
|
G | A | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8275G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101065 | ||||||
chr16:57101140
|
G | A | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8350G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101140 | ||||||
chr16:57101394
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+8604A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101394 | ||||||
chr16:57101419
|
G | A | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-36+8629G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101419 | ||||||
chr16:57101535
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-36+8745A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101535 | ||||||
chr16:57101592
|
CATT | C | 48 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0085others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36+8805_-36+8807d others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57101592 | |||||
chr16:57101680
|
C | T | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8890C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101680 | ||||||
chr16:57101681
|
G | C | 1 | a0001c0007t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36+8891G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101681 | ||||||
chr16:57101684
|
T | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8894T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101684 | ||||||
chr16:57101708
|
C | A | 39 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0166others(36): Show | 40 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-36+8918C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101708 | ||||||
chr16:57101708
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-36+8918C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101708 | ||||||
chr16:57101722
|
G | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8932G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101722 | ||||||
chr16:57101724
|
T | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02723.hp2 HG03471.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+8934T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101724 | ||||||
chr16:57101736
|
G | C | 1 | a0001c0001t0008g0106 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-36+8946G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101736 | ||||||
chr16:57101889
|
A | G | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8819A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101889 | ||||||
chr16:57101892
|
A | G | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8816A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101892 | ||||||
chr16:57101950
|
C | CT | 60 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0094others(57): Show | 61 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-35-8744dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57101950 | |||||
chr16:57101950
|
C | CTT | 39 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0166others(36): Show | 40 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-35-8745_-35-8744d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57101950 | |||||
chr16:57101971
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-35-8737G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101971 | ||||||
chr16:57102040
|
G | A | 1 | a0001c0001t0003g0320 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-35-8668G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102040 | ||||||
chr16:57102060
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-35-8648A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102060 | ||||||
chr16:57102079
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0153 | 3 | HG01891.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-35-8629C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102079 | ||||||
chr16:57102114
|
A | AT | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8585dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57102114 | |||||
chr16:57102171
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.-35-8537T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102171 | ||||||
chr16:57102196
|
T | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8512T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102196 | ||||||
chr16:57102246
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | HG01433.hp1 HG01496.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-8462G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102246 | ||||||
chr16:57102274
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0231a0001c0001t0001g0232others(10): Show | 14 | HG00639.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-35-8434G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102274 | ||||||
chr16:57102284
|
G | A | 3 | a0001c0001t0002g0098a0001c0005t0001g0007a0001c0005t0001g0097 | 4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-8424G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102284 | ||||||
chr16:57102295
|
A | G | 56 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8413A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102295 | ||||||
chr16:57102497
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0135others(8): Show | 11 | NA18951.hp1 NA18955.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35-8211C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102497 | ||||||
chr16:57102500
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-35-8208G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102500 | ||||||
chr16:57102502
|
C | T | 2 | a0001c0003t0001g0014a0001c0003t0001g0333 | 3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-35-8206C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102502 | ||||||
chr16:57102605
|
CT | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0192others(3): Show | 6 | HG00741.hp1 HG01074.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-8089delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57102605 | |||||
chr16:57102684
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-35-8024C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102684 | ||||||
chr16:57102703
|
G | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0107others(22): Show | 26 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35-8005G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102703 | ||||||
chr16:57103030
|
G | A | 3 | a0001c0001t0002g0098a0001c0005t0001g0007a0001c0005t0001g0097 | 4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-7678G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103030 | ||||||
chr16:57103097
|
C | T | 1 | a0001c0001t0003g0306 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-35-7611C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103097 | ||||||
chr16:57103175
|
C | G | 3 | a0001c0001t0002g0098a0001c0005t0001g0007a0001c0005t0001g0097 | 4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-7533C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103175 | ||||||
chr16:57103356
|
T | TCA | 70 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(67): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35-7351_-35-7350d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57103356 | |||||
chr16:57103543
|
C | G | 55 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0100others(52): Show | 56 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.-35-7165C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103543 | ||||||
chr16:57103573
|
C | G | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-35-7135C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103573 | ||||||
chr16:57103621
|
C | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 48 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-7087C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103621 | ||||||
chr16:57103733
|
C | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-6975C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103733 | ||||||
chr16:57104057
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-35-6651A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104057 | ||||||
chr16:57104162
|
G | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(239): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-35-6546G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104162 | ||||||
chr16:57104213
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-35-6495C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104213 | ||||||
chr16:57104217
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0149 | 2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-35-6491C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104217 | ||||||
chr16:57104218
|
G | A | 2 | a0001c0001t0001g0055a0003c0008t0001g0056 | 2 | NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-35-6490G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104218 | ||||||
chr16:57104295
|
G | C | 43 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0096others(40): Show | 44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-35-6413G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104295 | ||||||
chr16:57104352
|
T | G | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-35-6356T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104352 | ||||||
chr16:57104470
|
G | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0085others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-35-6238G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104470 | ||||||
chr16:57104512
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-35-6196G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104512 | ||||||
chr16:57104555
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-35-6153C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104555 | ||||||
chr16:57104567
|
C | T | 38 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0166others(35): Show | 39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-6141C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104567 | ||||||
chr16:57104985
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-5723G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104985 | ||||||
chr16:57105073
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-35-5635C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105073 | ||||||
chr16:57105157
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0312 | 2 | HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-35-5551C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105157 | ||||||
chr16:57105176
|
C | G | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-35-5532C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105176 | ||||||
chr16:57105430
|
G | GT | 15 | a0001c0001t0001g0035a0001c0001t0001g0053a0001c0001t0001g0091others(12): Show | 15 | HG00741.hp1 HG00741.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-35-5262dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57105430 | |||||
chr16:57105430
|
GT | G | 16 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0034others(13): Show | 20 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35-5262delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57105430 | |||||
chr16:57105435
|
T | G | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-35-5273T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105435 | ||||||
chr16:57105491
|
A | C | 1 | a0001c0001t0001g0243 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-35-5217A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105491 | ||||||
chr16:57105579
|
G | C | 10 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 11 | HG00673.hp1 HG02056.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-5129G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105579 | ||||||
chr16:57105627
|
G | A | 38 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0166others(35): Show | 39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-5081G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105627 | ||||||
chr16:57105692
|
T | G | 28 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0125others(25): Show | 28 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35-5016T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105692 | ||||||
chr16:57105722
|
A | G | 50 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0085others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-35-4986A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105722 | ||||||
chr16:57105735
|
A | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 48 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-4973A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105735 | ||||||
chr16:57105766
|
C | T | 3 | a0001c0001t0002g0098a0001c0005t0001g0007a0001c0005t0001g0097 | 4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-4942C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105766 | ||||||
chr16:57105773
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-35-4935G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105773 | ||||||
chr16:57105851
|
C | A | 20 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0200others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-35-4857C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105851 | ||||||
chr16:57105928
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35-4780C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105928 | ||||||
chr16:57105944
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-35-4764C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105944 | ||||||
chr16:57106180
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-35-4528T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106180 | ||||||
chr16:57106230
|
C | G | 100 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0019others(97): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35-4478C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106230 | ||||||
chr16:57106270
|
G | A | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(16): Show | 20 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35-4438G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106270 | ||||||
chr16:57106277
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-35-4431T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106277 | ||||||
chr16:57106345
|
C | T | 10 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-4363C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106345 | ||||||
chr16:57106526
|
G | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0091others(54): Show | 61 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(58): Show |
intron_variant | MODIFIER | c.-35-4182G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106526 | ||||||
chr16:57106550
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-4158G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106550 | ||||||
chr16:57106611
|
AGAAGAGA others(81): Show |
A | 1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-35-4095_-35-4008d others(90): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57106611 | |||||
chr16:57106858
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35-3850C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106858 | ||||||
chr16:57106864
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-35-3844C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106864 | ||||||
chr16:57106872
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0334others(11): Show | 18 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-35-3836C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106872 | ||||||
chr16:57107155
|
C | T | 3 | a0002c0004t0001g0039a0002c0004t0001g0040a0002c0004t0001g0162 | 3 | HG02622.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-3553C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107155 | ||||||
chr16:57107207
|
A | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(16): Show | 20 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35-3501A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107207 | ||||||
chr16:57107310
|
A | G | 38 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0166others(35): Show | 39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-3398A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107310 | ||||||
chr16:57107341
|
G | A | 20 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0200others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-35-3367G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107341 | ||||||
chr16:57107399
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 181 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.-35-3309A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107399 | ||||||
chr16:57107754
|
A | C | 71 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(68): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-35-2954A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107754 | ||||||
chr16:57107847
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-35-2861G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107847 | ||||||
chr16:57107865
|
C | CT | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0122others(32): Show | 35 | HG00597.hp2 HG01884.hp1 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-35-2820dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57107865 | |||||
chr16:57107865
|
CT | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-35-2820delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57107865 | |||||
chr16:57107914
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-35-2794A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107914 | ||||||
chr16:57107948
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0103others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-2760G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107948 | ||||||
chr16:57107961
|
C | G | 10 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-2747C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107961 | ||||||
chr16:57107964
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0003g0102 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-35-2744G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107964 | ||||||
chr16:57108241
|
A | C | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-35-2467A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108241 | ||||||
chr16:57108337
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35-2371C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108337 | ||||||
chr16:57108405
|
C | A | 1 | a0001c0001t0001g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-35-2303C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108405 | ||||||
chr16:57108991
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-35-1717T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108991 | ||||||
chr16:57109041
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0005g0038 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-35-1667T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109041 | ||||||
chr16:57109115
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-35-1593G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109115 | ||||||
chr16:57109201
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35-1507G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109201 | ||||||
chr16:57109265
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-35-1443C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109265 | ||||||
chr16:57109310
|
T | TA | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(18): Show | 22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35-1397dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57109310 | |||||
chr16:57109312
|
C | G | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(18): Show | 22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35-1396C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109312 | ||||||
chr16:57109470
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-35-1238T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109470 | ||||||
chr16:57109475
|
C | CA | 49 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-35-1217dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57109475 | |||||
chr16:57109475
|
C | CAA | 14 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0047others(11): Show | 18 | HG00438.hp1 HG02738.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.-35-1218_-35-1217d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57109475 | |||||
chr16:57109505
|
T | C | 15 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0108others(12): Show | 15 | HG00621.hp2 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-35-1203T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109505 | ||||||
chr16:57109518
|
A | G | 38 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0166others(35): Show | 39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-1190A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109518 | ||||||
chr16:57109703
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-35-1005C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109703 | ||||||
chr16:57109868
|
G | A | 2 | a0001c0003t0001g0014a0001c0003t0001g0333 | 3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-35-840G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109868 | ||||||
chr16:57109983
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-35-725T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109983 | ||||||
chr16:57110224
|
C | CTTT | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0334others(5): Show | 10 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-468_-35-466dup others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57110224 | |||||
chr16:57110224
|
CT | C | 36 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0091others(33): Show | 36 | HG01123.hp1 HG01175.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.-35-466delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57110224 | |||||
chr16:57110224
|
CTT | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-35-467_-35-466del others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57110224 | |||||
chr16:57110274
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-35-434G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110274 | ||||||
chr16:57110492
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-35-216A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110492 | ||||||
chr16:57110508
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-35-200G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110508 | ||||||
chr16:57110569
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-35-139T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110569 | ||||||
chr16:57110945
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.180+23C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57110945 | ||||||
chr16:57111008
|
T | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+86T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111008 | ||||||
chr16:57111009
|
G | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+87G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111009 | ||||||
chr16:57111113
|
TG | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+192delG | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111113 | ||||||
chr16:57111139
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180+217C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111139 | ||||||
chr16:57111182
|
C | CT | 49 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(46): Show | 54 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.180+274dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 57111182 | |||||
chr16:57111182
|
CT | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.180+274delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 57111182 | |||||
chr16:57111228
|
G | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0103others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+306G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111228 | ||||||
chr16:57111304
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+382T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111304 | ||||||
chr16:57111419
|
C | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0085others(18): Show | 22 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.180+497C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111419 | ||||||
chr16:57111428
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0193 | 2 | NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.180+506T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111428 | ||||||
chr16:57111439
|
A | G | 14 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG00408.hp1 HG02056.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+517A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111439 | ||||||
chr16:57111464
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.180+542C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111464 | ||||||
chr16:57111526
|
G | A | 2 | a0001c0005t0001g0007a0001c0005t0001g0097 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.180+604G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111526 | ||||||
chr16:57111590
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.180+668G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111590 | ||||||
chr16:57111992
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0003g0102 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+1070G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111992 | ||||||
chr16:57112113
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-1175A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112113 | ||||||
chr16:57112377
|
C | A | 43 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0049others(40): Show | 44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.181-911C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112377 | ||||||
chr16:57112379
|
G | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.181-909G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112379 | ||||||
chr16:57112490
|
C | T | 104 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0049others(101): Show | 105 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.181-798C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112490 | ||||||
chr16:57112692
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.181-596A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112692 | ||||||
chr16:57112744
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.181-544T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112744 | ||||||
chr16:57112768
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 194 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.181-520G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112768 | ||||||
chr16:57112789
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 170 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.181-499G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112789 | ||||||
chr16:57112879
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0201 | 3 | HG02895.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.181-409C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112879 | ||||||
chr16:57112942
|
C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.181-346C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112942 | ||||||
chr16:57112965
|
G | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.181-323G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112965 | ||||||
chr16:57112985
|
C | T | 43 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0049others(40): Show | 44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.181-303C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112985 | ||||||
chr16:57113225
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.181-63A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57113225 | ||||||
chr16:57113476
|
G | T | 80 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(77): Show | 84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.360+9G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113476 | ||||||
chr16:57113479
|
C | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0097 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.360+12C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113479 | ||||||
chr16:57113536
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.360+69C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113536 | ||||||
chr16:57113580
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.360+113G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113580 | ||||||
chr16:57113610
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.360+143C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113610 | ||||||
chr16:57113714
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.360+247A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113714 | ||||||
chr16:57113735
|
C | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0097 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.360+268C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113735 | ||||||
chr16:57113776
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+309C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113776 | ||||||
chr16:57113862
|
G | T | 9 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0243others(6): Show | 9 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+395G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113862 | ||||||
chr16:57113940
|
T | G | 40 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0092others(37): Show | 40 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.360+473T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113940 | ||||||
chr16:57114019
|
C | CT | 3 | a0001c0001t0001g0305a0001c0001t0001g0339a0001c0001t0003g0320 | 3 | HG03195.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.360+553dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114019 | |||||
chr16:57114033
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+566T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114033 | ||||||
chr16:57114041
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+574A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114041 | ||||||
chr16:57114143
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+676G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114143 | ||||||
chr16:57114182
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.360+715G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114182 | ||||||
chr16:57114393
|
G | C | 1 | a0001c0001t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.360+926G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114393 | ||||||
chr16:57114437
|
CG | C | 15 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0161others(12): Show | 15 | HG00099.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.360+975delG | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114437 | |||||
chr16:57114444
|
C | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0002t0001g0069 | 3 | HG00609.hp1 NA19088.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.360+977C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114444 | ||||||
chr16:57114457
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.360+990G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114457 | ||||||
chr16:57114536
|
C | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0097 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.361-940C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114536 | ||||||
chr16:57114538
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-938C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114538 | ||||||
chr16:57114570
|
C | T | 43 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0049others(40): Show | 44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.361-906C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114570 | ||||||
chr16:57114573
|
C | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-903C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114573 | ||||||
chr16:57114641
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.361-835G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114641 | ||||||
chr16:57114661
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.361-815G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114661 | ||||||
chr16:57114775
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-701A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114775 | ||||||
chr16:57114789
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-687T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114789 | ||||||
chr16:57114803
|
A | AATAG | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-671_361-668dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114803 | |||||
chr16:57114878
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.361-598G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114878 | ||||||
chr16:57114907
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-569A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114907 | ||||||
chr16:57114934
|
C | CA | 61 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(58): Show | 64 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.361-516dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CAA | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0049others(15): Show | 18 | HG00544.hp2 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-517_361-516dup others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CAAA | 11 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0105others(8): Show | 11 | HG02559.hp2 HG02895.hp2 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.361-518_361-516dup others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CAAAA | 35 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0085others(32): Show | 36 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.361-519_361-516dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CAAAAA | 17 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0094others(14): Show | 17 | HG00280.hp2 HG00735.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.361-520_361-516dup others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CAAAAAA | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0041others(35): Show | 40 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.361-521_361-516dup others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CAAAAAAA | 19 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0055others(16): Show | 22 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.361-522_361-516dup others(7): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114934
|
C | CCAA | 19 | a0001c0001t0001g0099a0001c0001t0001g0110a0001c0001t0001g0111others(16): Show | 19 | HG00099.hp2 HG01255.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.361-542_361-541ins others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114934 | ||||||
chr16:57114934
|
C | CCAAA | 7 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0143others(4): Show | 7 | HG01123.hp1 HG01175.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-542_361-541ins others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114934 | ||||||
chr16:57114934
|
CA | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0118a0001c0001t0001g0119others(7): Show | 11 | HG00597.hp2 HG01070.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-516delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | |||||
chr16:57114935
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.361-541A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114935 | ||||||
chr16:57114968
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00408.hp1 HG02056.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-508G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114968 | ||||||
chr16:57115002
|
G | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.361-474G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115002 | ||||||
chr16:57115005
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.361-471G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115005 | ||||||
chr16:57115015
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.361-461G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115015 | ||||||
chr16:57115046
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.361-430G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115046 | ||||||
chr16:57115115
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.361-361A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115115 | ||||||
chr16:57115262
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.361-214C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115262 | ||||||
chr16:57115335
|
G | A | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02723.hp2 HG03471.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-141G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115335 | ||||||
chr16:57115370
|
G | A | 3 | a0002c0004t0001g0039a0002c0004t0001g0040a0002c0004t0001g0162 | 3 | HG02622.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.361-106G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115370 | ||||||
chr16:57115406
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01069.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.361-70G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115406 | ||||||
chr16:57115452
|
C | T | 1 | a0001c0003t0003g0276 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.361-24C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115452 | ||||||
chr16:57115729
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.435+179G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57115729 | ||||||
chr16:57115733
|
C | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 57 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.435+183C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57115733 | ||||||
chr16:57115802
|
C | T | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.435+252C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57115802 | ||||||
chr16:57116066
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.435+516C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116066 | ||||||
chr16:57116108
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.435+558C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116108 | ||||||
chr16:57116279
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0334a0001c0001t0001g0335others(2): Show | 6 | HG02055.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+729C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116279 | ||||||
chr16:57116337
|
G | A | 41 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0049others(38): Show | 42 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.435+787G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116337 | ||||||
chr16:57116498
|
G | A | 2 | a0002c0004t0001g0039a0002c0004t0001g0040 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.435+948G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116498 | ||||||
chr16:57116501
|
A | G | 1 | a0001c0002t0001g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.435+951A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116501 | ||||||
chr16:57116580
|
C | T | 1 | a0001c0002t0001g0138 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.436-916C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116580 | ||||||
chr16:57116594
|
C | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(99): Show | 111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.436-902C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116594 | ||||||
chr16:57116661
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.436-835C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116661 | ||||||
chr16:57116765
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0180 | 2 | HG00558.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.436-731G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116765 | ||||||
chr16:57116852
|
G | GAGGCCCC others(6): Show |
1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.436-633_436-621dup others(13): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 57116852 | |||||
chr16:57116897
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.436-599G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116897 | ||||||
chr16:57116935
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0160a0001c0001t0001g0334others(2): Show | 6 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-561T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116935 | ||||||
chr16:57116975
|
G | A | 2 | a0001c0001t0001g0303a0001c0001t0002g0098 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.436-521G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116975 | ||||||
chr16:57117031
|
T | G | 6 | a0001c0001t0001g0231a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG00639.hp1 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-465T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117031 | ||||||
chr16:57117194
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0270 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.436-302G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117194 | ||||||
chr16:57117263
|
A | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 63 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.436-233A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117263 | ||||||
chr16:57117314
|
G | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0005g0038others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-182G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117314 | ||||||
chr16:57117472
|
G | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0232others(4): Show | 8 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-24G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117472 | ||||||
chr16:57117630
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.507+63G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117630 | ||||||
chr16:57117647
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.507+80C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117647 | ||||||
chr16:57117704
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0201a0001c0001t0002g0321others(2): Show | 5 | HG02647.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+137G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117704 | ||||||
chr16:57117884
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.507+317C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117884 | ||||||
chr16:57117885
|
G | A | 13 | a0001c0001t0001g0037a0001c0001t0001g0103a0001c0001t0001g0150others(10): Show | 14 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.507+318G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117885 | ||||||
chr16:57117942
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.507+375C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117942 | ||||||
chr16:57118082
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0005g0038others(3): Show | 7 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+515G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118082 | ||||||
chr16:57118129
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.507+562G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118129 | ||||||
chr16:57118142
|
T | C | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.507+575T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118142 | ||||||
chr16:57118167
|
C | CT | 15 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0105others(12): Show | 15 | NA18944.hp1 NA18955.hp1 NA18969.hp2 others(12): Show |
intron_variant | MODIFIER | c.507+616dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118167 | |||||
chr16:57118167
|
CT | C | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 61 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.507+616delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118167 | |||||
chr16:57118250
|
C | G | 28 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0166others(25): Show | 29 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.507+683C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118250 | ||||||
chr16:57118311
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.507+744G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118311 | ||||||
chr16:57118322
|
C | T | 6 | a0001c0001t0001g0290a0001c0001t0001g0305a0001c0001t0001g0339others(3): Show | 6 | HG02647.hp1 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+755C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118322 | ||||||
chr16:57118332
|
A | ATT | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 61 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.507+778_507+779dup others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | |||||
chr16:57118332
|
A | ATTT | 7 | a0001c0001t0001g0095a0001c0001t0001g0125a0001c0001t0001g0247others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+777_507+779dup others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | |||||
chr16:57118332
|
A | ATTTT | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.507+776_507+779dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | |||||
chr16:57118332
|
A | ATTTTT | 6 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0182others(3): Show | 7 | HG01099.hp1 HG01109.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+775_507+779dup others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | |||||
chr16:57118332
|
AT | A | 55 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(52): Show | 57 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.507+779delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | |||||
chr16:57118524
|
A | C | 10 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0243others(7): Show | 10 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.508-671A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118524 | ||||||
chr16:57118564
|
C | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0205a0001c0001t0001g0247others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-631C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118564 | ||||||
chr16:57118648
|
A | AGATG | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.508-507_508-504dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | |||||
chr16:57118648
|
A | AGATGGAT others(1): Show |
24 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0068others(21): Show | 26 | HG00280.hp2 HG00544.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.508-511_508-504dup others(8): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | |||||
chr16:57118648
|
A | AGATGGAT others(5): Show |
1 | a0001c0001t0001g0308 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-515_508-504dup others(12): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | |||||
chr16:57118648
|
AGATGGAT others(5): Show |
A | 2 | a0001c0001t0001g0127a0001c0001t0001g0157 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508-515_508-504del others(12): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | |||||
chr16:57118668
|
GGATGGAT others(17): Show |
G | 1 | a0001c0002t0001g0021 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.508-523_508-500del others(24): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118668 | |||||
chr16:57118688
|
G | GGATGGAT others(1): Show |
3 | a0001c0001t0001g0206a0001c0001t0001g0218a0001c0001t0001g0291 | 3 | HG00323.hp1 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.508-504_508-503ins others(8): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118688 | |||||
chr16:57118688
|
GGATA | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0005g0038others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-488_508-485del others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118688 | |||||
chr16:57118692
|
A | G | 51 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(48): Show | 53 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-503A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118692 | ||||||
chr16:57118696
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0005g0038others(3): Show | 7 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-499A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118696 | ||||||
chr16:57118720
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.508-475A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118720 | ||||||
chr16:57118894
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 62 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.508-301C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118894 | ||||||
chr16:57118900
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0218 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.508-295A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118900 | ||||||
chr16:57118958
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0002g0153 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.508-237G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118958 | ||||||
chr16:57119020
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0002g0153 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.508-175A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57119020 | ||||||
chr16:57119107
|
G | A | 34 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0166others(31): Show | 35 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.508-88G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57119107 | ||||||
chr16:57119491
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.592-70T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 6/15 | chr16 | 57119491 | ||||||
chr16:57119529
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 62 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.592-32C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 6/15 | chr16 | 57119529 | ||||||
chr16:57119655
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.681+5G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57119655 | ||||||
chr16:57119952
|
A | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0201a0001c0001t0002g0123others(1): Show | 4 | HG02895.hp1 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+302A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57119952 | ||||||
chr16:57120005
|
TCTCATGC others(295): Show |
T | 1 | a0001c0001t0001g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.681+388_681+689del | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120005 | |||||
chr16:57120195
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.681+545T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120195 | ||||||
chr16:57120244
|
A | C | 1 | a0001c0002t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.681+594A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120244 | ||||||
chr16:57120270
|
C | CA | 48 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0094others(45): Show | 49 | HG00558.hp2 HG00673.hp1 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.681+636dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120270 | |||||
chr16:57120286
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 89 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.681+636A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120286 | ||||||
chr16:57120297
|
G | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(136): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.681+647G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120297 | ||||||
chr16:57120378
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.682-715C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120378 | ||||||
chr16:57120439
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.682-639delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120439 | |||||
chr16:57120439
|
CAA | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG00408.hp2 HG01243.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-640_682-639del others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120439 | |||||
chr16:57120635
|
A | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 326 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.682-458A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120635 | ||||||
chr16:57120635
|
A | T | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.682-458A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120635 | ||||||
chr16:57120774
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.682-319G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120774 | ||||||
chr16:57121075
|
G | C | 2 | a0001c0001t0003g0102a0002c0004t0001g0162 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682-18G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57121075 | ||||||
chr16:57121286
|
C | T | 4 | a0001c0001t0001g0290a0001c0001t0001g0305a0001c0001t0001g0339others(1): Show | 4 | HG03139.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+95C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121286 | ||||||
chr16:57121484
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(134): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.781-190G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121484 | ||||||
chr16:57121545
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.781-129T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121545 | ||||||
chr16:57121566
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.781-108C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121566 | ||||||
chr16:57121649
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.781-25T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121649 | ||||||
chr16:57121770
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.867+10C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121770 | ||||||
chr16:57121782
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.867+22C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121782 | ||||||
chr16:57121783
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0305a0001c0001t0001g0339others(1): Show | 4 | HG03139.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+23G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121783 | ||||||
chr16:57121888
|
T | A | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.867+128T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121888 | ||||||
chr16:57122023
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.867+263C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122023 | ||||||
chr16:57122056
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.867+296A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122056 | ||||||
chr16:57122083
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(194): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.867+323G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122083 | ||||||
chr16:57122165
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.867+405G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122165 | ||||||
chr16:57122417
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0250 | 2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.867+657A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122417 | ||||||
chr16:57122454
|
A | G | 9 | a0001c0001t0001g0103a0001c0001t0001g0290a0001c0001t0001g0305others(6): Show | 9 | HG02647.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.867+694A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122454 | ||||||
chr16:57122546
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.867+786C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122546 | ||||||
chr16:57122593
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0313a0001c0005t0001g0097 | 3 | HG02818.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.868-821T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122593 | ||||||
chr16:57122797
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-617C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122797 | ||||||
chr16:57122887
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.868-527C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122887 | ||||||
chr16:57122905
|
CT | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(197): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.868-494delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 57122905 | |||||
chr16:57123119
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.868-295T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123119 | ||||||
chr16:57123123
|
G | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(189): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.868-291G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123123 | ||||||
chr16:57123133
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.868-281G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123133 | ||||||
chr16:57123137
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.868-277G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123137 | ||||||
chr16:57123258
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.868-156A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123258 | ||||||
chr16:57123294
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(129): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.868-120C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123294 | ||||||
chr16:57123297
|
A | G | 3 | a0001c0005t0001g0007a0001c0007t0001g0090a0001c0007t0001g0302 | 4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-117A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123297 | ||||||
chr16:57123346
|
G | A | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.868-68G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123346 | ||||||
chr16:57123488
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.927+15G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123488 | ||||||
chr16:57123524
|
C | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0313a0001c0005t0001g0097 | 3 | HG02818.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.927+51C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123524 | ||||||
chr16:57123529
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+56T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123529 | ||||||
chr16:57123592
|
G | T | 1 | a0001c0001t0001g0016 | 2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.927+119G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123592 | ||||||
chr16:57123674
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.927+201A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123674 | ||||||
chr16:57123917
|
TC | T | 53 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0023others(50): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.927+447delC | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57123917 | |||||
chr16:57124063
|
CTTTCT | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0103others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+614_927+618del others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124063 | |||||
chr16:57124063
|
CTTTCTTT others(8): Show |
C | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+604_927+618del others(15): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124063 | |||||
chr16:57124082
|
CTTTTCTT others(3): Show |
C | 34 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(31): Show | 36 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.927+614_927+623del others(10): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124082 | |||||
chr16:57124087
|
C | CT | 11 | a0001c0001t0001g0075a0001c0001t0001g0146a0001c0001t0001g0147others(8): Show | 11 | HG02451.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+626dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124087 | |||||
chr16:57124108
|
G | T | 2 | a0001c0001t0001g0037a0001c0001t0005g0038 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.927+635G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124108 | ||||||
chr16:57124122
|
C | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(31): Show | 36 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.927+649C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124122 | ||||||
chr16:57124200
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.927+727G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124200 | ||||||
chr16:57124438
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+965C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124438 | ||||||
chr16:57124440
|
C | A | 14 | a0001c0001t0001g0016a0001c0001t0001g0200a0001c0001t0001g0214others(11): Show | 16 | HG00323.hp2 HG01515.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.927+967C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124440 | ||||||
chr16:57124552
|
A | C | 1 | a0001c0001t0002g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.927+1079A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124552 | ||||||
chr16:57124716
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-1144A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124716 | ||||||
chr16:57124767
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(222): Show | 237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.928-1093G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124767 | ||||||
chr16:57124935
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.928-925C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124935 | ||||||
chr16:57124960
|
C | T | 17 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0094others(14): Show | 17 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-900C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124960 | ||||||
chr16:57124995
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(176): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.928-865C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124995 | ||||||
chr16:57125055
|
C | G | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928-805C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125055 | ||||||
chr16:57125321
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.928-539A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125321 | ||||||
chr16:57125336
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(224): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.928-524C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125336 | ||||||
chr16:57125490
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(224): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.928-370A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125490 | ||||||
chr16:57125613
|
G | T | 3 | a0001c0005t0001g0007a0001c0007t0001g0090a0001c0007t0001g0302 | 4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-247G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125613 | ||||||
chr16:57125633
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0002g0153 | 2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.928-227C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125633 | ||||||
chr16:57125663
|
A | C | 1 | a0001c0001t0001g0237 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.928-197A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125663 | ||||||
chr16:57125777
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0307 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.928-83A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125777 | ||||||
chr16:57126114
|
T | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(39): Show | 44 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1061+121T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126114 | ||||||
chr16:57126180
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1061+187C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126180 | ||||||
chr16:57126205
|
A | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0200a0001c0001t0001g0214others(10): Show | 15 | HG00323.hp2 HG01515.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1061+212A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126205 | ||||||
chr16:57126277
|
A | G | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1061+284A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126277 | ||||||
chr16:57126326
|
G | A | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(7): Show | 10 | HG01123.hp1 HG01175.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1061+333G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126326 | ||||||
chr16:57126340
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1061+347G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126340 | ||||||
chr16:57126427
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(32): Show | 37 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1061+434T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126427 | ||||||
chr16:57126502
|
G | A | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+509G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126502 | ||||||
chr16:57126526
|
T | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(163): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1061+533T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126526 | ||||||
chr16:57126526
|
T | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0200a0001c0001t0001g0214others(10): Show | 15 | HG00323.hp2 HG01515.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1061+533T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126526 | ||||||
chr16:57126560
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | HG01123.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1061+567G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126560 | ||||||
chr16:57126931
|
C | G | 2 | a0001c0001t0001g0091a0002c0004t0001g0040 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1062-918C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126931 | ||||||
chr16:57126957
|
C | G | 21 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1062-892C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126957 | ||||||
chr16:57126995
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1062-854C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126995 | ||||||
chr16:57127108
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0088a0001c0001t0005g0038 | 3 | HG02559.hp2 HG02809.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1062-741C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127108 | ||||||
chr16:57127131
|
C | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(31): Show | 36 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1062-718C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127131 | ||||||
chr16:57127200
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1062-649G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127200 | ||||||
chr16:57127348
|
G | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0192 | 2 | NA18950.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1062-501G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127348 | ||||||
chr16:57127544
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1062-305G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127544 | ||||||
chr16:57127592
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0143a0001c0001t0001g0215others(1): Show | 5 | HG00738.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-257T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127592 | ||||||
chr16:57127771
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1062-78G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127771 | ||||||
chr16:57127785
|
G | GGTTCCTG others(35): Show |
2 | a0001c0001t0001g0037a0001c0001t0005g0038 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1062-63_1062-62ins others(42): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 57127785 | |||||
chr16:57127796
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0002g0104 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1062-53C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127796 | ||||||
chr16:57127916
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0292 | 2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1116+13G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57127916 | ||||||
chr16:57128070
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1116+167C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128070 | ||||||
chr16:57128341
|
T | C | 2 | a0001c0002t0001g0198a0001c0006t0001g0199 | 2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1116+438T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128341 | ||||||
chr16:57128378
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1116+475C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128378 | ||||||
chr16:57128520
|
A | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(241): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1116+617A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128520 | ||||||
chr16:57128659
|
G | A | 1 | a0001c0005t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1116+756G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128659 | ||||||
chr16:57128744
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(196): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1116+841G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128744 | ||||||
chr16:57128752
|
T | C | 2 | a0001c0002t0001g0194a0001c0002t0001g0293 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1116+849T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128752 | ||||||
chr16:57128769
|
T | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(40): Show | 45 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1116+866T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128769 | ||||||
chr16:57129005
|
A | G | 6 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0158others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+1102A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129005 | ||||||
chr16:57129119
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0005g0038 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1116+1216G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129119 | ||||||
chr16:57129216
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1116+1313G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129216 | ||||||
chr16:57129218
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1116+1315G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129218 | ||||||
chr16:57129237
|
A | C | 1 | a0001c0002t0001g0170 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1116+1334A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129237 | ||||||
chr16:57129295
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0266 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1116+1392C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129295 | ||||||
chr16:57129306
|
C | T | 2 | a0001c0002t0001g0228a0001c0002t0001g0229 | 2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1116+1403C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129306 | ||||||
chr16:57129471
|
G | A | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1116+1568G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129471 | ||||||
chr16:57129635
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(33): Show | 38 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1116+1732A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129635 | ||||||
chr16:57129789
|
A | G | 7 | a0001c0001t0001g0200a0001c0001t0001g0214a0001c0001t0001g0339others(4): Show | 7 | HG00323.hp2 HG01515.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116+1886A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129789 | ||||||
chr16:57129869
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1116+1966A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129869 | ||||||
chr16:57130127
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(32): Show | 37 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1116+2224T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130127 | ||||||
chr16:57130176
|
C | T | 2 | a0001c0001t0003g0102a0002c0004t0001g0162 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1116+2273C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130176 | ||||||
chr16:57130269
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1116+2366C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130269 | ||||||
chr16:57130342
|
A | G | 9 | a0001c0001t0001g0070a0001c0001t0001g0241a0001c0001t0001g0256others(6): Show | 9 | HG00438.hp2 HG00741.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1116+2439A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130342 | ||||||
chr16:57130400
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG03017.hp1 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1116+2497A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130400 | ||||||
chr16:57130431
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1116+2528C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130431 | ||||||
chr16:57130432
|
G | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1116+2529G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130432 | ||||||
chr16:57130445
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0284others(5): Show | 9 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1116+2542G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130445 | ||||||
chr16:57130566
|
A | G | 6 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0158others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+2663A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130566 | ||||||
chr16:57130616
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0002t0001g0198others(1): Show | 4 | HG00673.hp1 HG02056.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+2713C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130616 | ||||||
chr16:57130699
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | NA18949.hp2 NA18979.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1116+2796G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130699 | ||||||
chr16:57130967
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1116+3064C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130967 | ||||||
chr16:57130968
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0303 | 3 | HG01123.hp2 HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1116+3065G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130968 | ||||||
chr16:57131051
|
A | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(251): Show | 266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1116+3148A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131051 | ||||||
chr16:57131089
|
A | C | 3 | a0001c0005t0001g0007a0001c0007t0001g0090a0001c0007t0001g0302 | 4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+3186A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131089 | ||||||
chr16:57131148
|
T | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1116+3245T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131148 | ||||||
chr16:57131151
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1116+3248G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131151 | ||||||
chr16:57131257
|
C | A | 6 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0158others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+3354C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131257 | ||||||
chr16:57131469
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1117-3306G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131469 | ||||||
chr16:57131470
|
G | T | 1 | a0001c0002t0001g0263 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1117-3305G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131470 | ||||||
chr16:57131617
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1117-3158G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131617 | ||||||
chr16:57131633
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1117-3142C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131633 | ||||||
chr16:57131711
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1117-3064C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131711 | ||||||
chr16:57131725
|
C | T | 2 | a0001c0001t0001g0339a0001c0001t0002g0286 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1117-3050C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131725 | ||||||
chr16:57131836
|
G | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0023others(50): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1117-2939G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131836 | ||||||
chr16:57132066
|
G | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0023others(50): Show | 55 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1117-2709G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132066 | ||||||
chr16:57132275
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1117-2500G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132275 | ||||||
chr16:57132306
|
C | G | 1 | a0001c0002t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1117-2469C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132306 | ||||||
chr16:57132315
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1117-2460G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132315 | ||||||
chr16:57132317
|
G | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0020others(36): Show | 42 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1117-2458G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132317 | ||||||
chr16:57132334
|
T | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0020others(36): Show | 42 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1117-2441T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132334 | ||||||
chr16:57132626
|
A | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(40): Show | 45 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1117-2149A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132626 | ||||||
chr16:57132864
|
C | T | 1 | a0001c0002t0001g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1117-1911C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132864 | ||||||
chr16:57132869
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1117-1906G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132869 | ||||||
chr16:57132869
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1117-1906G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132869 | ||||||
chr16:57132991
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1117-1784A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132991 | ||||||
chr16:57132992
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1117-1783T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132992 | ||||||
chr16:57132993
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1117-1782C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132993 | ||||||
chr16:57133000
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1117-1775G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133000 | ||||||
chr16:57133073
|
T | C | 7 | a0001c0001t0001g0200a0001c0001t0001g0214a0001c0001t0001g0339others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-1702T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133073 | ||||||
chr16:57133104
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1117-1671C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133104 | ||||||
chr16:57133268
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(33): Show | 38 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1117-1507C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133268 | ||||||
chr16:57133318
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1117-1457G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133318 | ||||||
chr16:57133465
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0214 | 2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1117-1310C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133465 | ||||||
chr16:57133567
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1117-1208C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133567 | ||||||
chr16:57133706
|
C | T | 44 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0029others(41): Show | 47 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1117-1069C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133706 | ||||||
chr16:57133755
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1117-1020G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133755 | ||||||
chr16:57133889
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1117-886C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133889 | ||||||
chr16:57133890
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1117-885G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133890 | ||||||
chr16:57133992
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1117-783G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133992 | ||||||
chr16:57134047
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1117-728G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134047 | ||||||
chr16:57134102
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1117-673A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134102 | ||||||
chr16:57134125
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1117-650C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134125 | ||||||
chr16:57134260
|
C | G | 3 | a0001c0001t0001g0305a0001c0001t0002g0123a0001c0001t0002g0271 | 3 | HG02145.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1117-515C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134260 | ||||||
chr16:57134320
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1117-455A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134320 | ||||||
chr16:57134385
|
G | A | 1 | a0001c0002t0004g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1117-390G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134385 | ||||||
chr16:57134422
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1117-353G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134422 | ||||||
chr16:57134523
|
A | G | 43 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0029others(40): Show | 46 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.1117-252A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134523 | ||||||
chr16:57134544
|
G | A | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265 | 3 | HG00438.hp2 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1117-231G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134544 | ||||||
chr16:57134629
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1117-146G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134629 | ||||||
chr16:57134654
|
G | A | 1 | a0001c0005t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1117-121G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134654 | ||||||
chr16:57134710
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1117-65G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134710 | ||||||
chr16:57134739
|
G | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0029others(41): Show | 47 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.1117-36G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134739 | ||||||
chr16:57134945
|
T | C | 4 | a0001c0001t0001g0305a0001c0001t0002g0123a0001c0001t0002g0271others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168+119T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57134945 | ||||||
chr16:57134951
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1168+125T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57134951 | ||||||
chr16:57135239
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1168+413T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135239 | ||||||
chr16:57135280
|
CA | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 158 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1168+455delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135280 | ||||||
chr16:57135373
|
A | G | 1 | a0001c0002t0001g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1168+547A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135373 | ||||||
chr16:57135395
|
G | A | 2 | a0001c0002t0001g0196a0001c0002t0001g0293 | 2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1168+569G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135395 | ||||||
chr16:57135574
|
G | A | 1 | a0001c0003t0001g0333 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1168+748G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135574 | ||||||
chr16:57135646
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0335 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1168+820G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135646 | ||||||
chr16:57135661
|
G | A | 3 | a0001c0005t0001g0007a0001c0007t0001g0090a0001c0007t0001g0302 | 4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168+835G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135661 | ||||||
chr16:57135851
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0271a0001c0001t0002g0286 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1168+1025G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135851 | ||||||
chr16:57135873
|
CA | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1168+1065delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57135873 | |||||
chr16:57135873
|
CAA | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0148a0001c0001t0001g0234others(4): Show | 7 | HG01169.hp2 HG01515.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1064_1168+106 others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57135873 | |||||
chr16:57135962
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1168+1136G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135962 | ||||||
chr16:57135978
|
G | A | 6 | a0001c0001t0001g0339a0001c0001t0003g0164a0001c0001t0003g0220others(3): Show | 6 | HG00280.hp2 HG01515.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+1152G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135978 | ||||||
chr16:57136047
|
GAAGA | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0271a0001c0001t0002g0286 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1169-1091_1169-108 others(8): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57136047 | |||||
chr16:57136057
|
A | C | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1169-1092A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136057 | ||||||
chr16:57136110
|
ACT | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0029others(41): Show | 47 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.1169-1036_1169-103 others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57136110 | |||||
chr16:57136277
|
T | C | 6 | a0001c0001t0001g0339a0001c0001t0003g0164a0001c0001t0003g0220others(3): Show | 6 | HG00280.hp2 HG01515.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1169-872T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136277 | ||||||
chr16:57136842
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1169-307G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136842 | ||||||
chr16:57136946
|
G | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0044others(40): Show | 46 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.1169-203G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136946 | ||||||
chr16:57137024
|
G | C | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0087others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1169-125G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57137024 | ||||||
chr16:57137321
|
C | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1302+39C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137321 | ||||||
chr16:57137325
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1302+43C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137325 | ||||||
chr16:57137485
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1302+203C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137485 | ||||||
chr16:57137553
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+271A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137553 | ||||||
chr16:57137591
|
T | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0082others(1): Show | 4 | HG02071.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+309T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137591 | ||||||
chr16:57137645
|
C | G | 2 | a0001c0001t0002g0124a0001c0001t0002g0322 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1302+363C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137645 | ||||||
chr16:57137653
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0318 | 2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1302+371G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137653 | ||||||
chr16:57137728
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(107): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1302+446G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137728 | ||||||
chr16:57137924
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1302+642A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137924 | ||||||
chr16:57138095
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0292 | 2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1302+813C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138095 | ||||||
chr16:57138107
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(107): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1302+825G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138107 | ||||||
chr16:57138120
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1302+838C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138120 | ||||||
chr16:57138195
|
C | T | 14 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(11): Show | 15 | HG00280.hp2 HG01123.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+913C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138195 | ||||||
chr16:57138273
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1302+991T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138273 | ||||||
chr16:57138343
|
C | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+1061C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138343 | ||||||
chr16:57138421
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+1139G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138421 | ||||||
chr16:57138492
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0318 | 2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1302+1210C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138492 | ||||||
chr16:57138632
|
C | A | 1 | a0001c0002t0004g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1302+1350C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138632 | ||||||
chr16:57138652
|
A | AC | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1302+1371dupC | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57138652 | |||||
chr16:57138717
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1302+1435T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138717 | ||||||
chr16:57138946
|
C | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0097 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+1664C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138946 | ||||||
chr16:57138947
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0281others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+1665G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138947 | ||||||
chr16:57138979
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1302+1697A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138979 | ||||||
chr16:57138996
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1302+1714T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138996 | ||||||
chr16:57139059
|
G | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1302+1777G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139059 | ||||||
chr16:57139066
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1302+1784G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139066 | ||||||
chr16:57139096
|
T | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1302+1814T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139096 | ||||||
chr16:57139099
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1302+1817C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139099 | ||||||
chr16:57139168
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1302+1886A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139168 | ||||||
chr16:57139358
|
A | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0097 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+2076A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139358 | ||||||
chr16:57139616
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1302+2334C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139616 | ||||||
chr16:57139717
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1302+2435T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139717 | ||||||
chr16:57139735
|
C | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1302+2453C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139735 | ||||||
chr16:57139762
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1302+2480A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139762 | ||||||
chr16:57139855
|
C | T | 6 | a0001c0001t0001g0339a0001c0001t0003g0164a0001c0001t0003g0220others(3): Show | 6 | HG00280.hp2 HG01515.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+2573C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139855 | ||||||
chr16:57140042
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+2760G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140042 | ||||||
chr16:57140050
|
A | G | 1 | a0001c0002t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1302+2768A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140050 | ||||||
chr16:57140093
|
C | T | 2 | a0001c0001t0002g0271a0001c0001t0002g0286 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1302+2811C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140093 | ||||||
chr16:57140223
|
TGCAATGG others(3): Show |
T | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1302+2942_1302+295 others(14): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140223 | ||||||
chr16:57140254
|
T | G | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1302+2972T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140254 | ||||||
chr16:57140284
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1302+3002T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140284 | ||||||
chr16:57140296
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1302+3014A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140296 | ||||||
chr16:57140415
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1302+3133G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140415 | ||||||
chr16:57140589
|
A | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0214 | 2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1302+3307A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140589 | ||||||
chr16:57140775
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1302+3493C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140775 | ||||||
chr16:57140785
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1302+3503G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140785 | ||||||
chr16:57140798
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0061 | 3 | HG00408.hp1 HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1302+3516C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140798 | ||||||
chr16:57140810
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+3528C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140810 | ||||||
chr16:57140820
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+3538C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140820 | ||||||
chr16:57140868
|
AT | A | 28 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0062others(25): Show | 28 | HG01952.hp1 HG02280.hp2 HG02572.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+3613delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57140868 | |||||
chr16:57140868
|
ATT | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1302+3612_1302+361 others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57140868 | |||||
chr16:57140868
|
ATTT | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0016others(66): Show | 74 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1302+3611_1302+361 others(7): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57140868 | |||||
chr16:57140871
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0053 | 2 | NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1302+3589T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140871 | ||||||
chr16:57140985
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1302+3703G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140985 | ||||||
chr16:57141079
|
G | A | 45 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0029others(42): Show | 48 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.1302+3797G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141079 | ||||||
chr16:57141193
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1302+3911G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141193 | ||||||
chr16:57141315
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1302+4033C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141315 | ||||||
chr16:57141837
|
T | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-4248T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141837 | ||||||
chr16:57142376
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0248a0001c0001t0001g0250 | 4 | HG02258.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-3709G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142376 | ||||||
chr16:57142389
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0149 | 2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1303-3696C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142389 | ||||||
chr16:57142390
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303-3695G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142390 | ||||||
chr16:57142495
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1303-3590C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142495 | ||||||
chr16:57142670
|
G | C | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1303-3415G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142670 | ||||||
chr16:57142737
|
A | G | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1303-3348A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142737 | ||||||
chr16:57142751
|
C | A | 1 | a0001c0001t0002g0210 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1303-3334C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142751 | ||||||
chr16:57142756
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0128a0001c0001t0001g0160others(2): Show | 6 | HG01891.hp1 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-3329C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142756 | ||||||
chr16:57143033
|
C | T | 1 | a0001c0003t0003g0276 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1303-3052C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143033 | ||||||
chr16:57143055
|
C | G | 10 | a0001c0001t0001g0339a0001c0001t0003g0102a0001c0001t0003g0164others(7): Show | 11 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303-3030C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143055 | ||||||
chr16:57143082
|
CT | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(1): Show | 4 | HG01123.hp2 HG01884.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-3001delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57143082 | |||||
chr16:57143107
|
C | T | 1 | a0001c0005t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1303-2978C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143107 | ||||||
chr16:57143202
|
G | C | 1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1303-2883G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143202 | ||||||
chr16:57143343
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1303-2742C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143343 | ||||||
chr16:57144135
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0318 | 2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1303-1950C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144135 | ||||||
chr16:57144501
|
G | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(3): Show | 6 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-1584G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144501 | ||||||
chr16:57144591
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1303-1494G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144591 | ||||||
chr16:57144762
|
A | T | 6 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0284others(3): Show | 6 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-1323A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144762 | ||||||
chr16:57144763
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1303-1322C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144763 | ||||||
chr16:57144954
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1303-1131G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144954 | ||||||
chr16:57145028
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1303-1057G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145028 | ||||||
chr16:57145298
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1303-787G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145298 | ||||||
chr16:57145348
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1303-737T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145348 | ||||||
chr16:57145383
|
C | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG00639.hp1 HG01074.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-702C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145383 | ||||||
chr16:57145490
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1303-595G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145490 | ||||||
chr16:57145491
|
A | ACCTGCTT others(5): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0248a0001c0001t0001g0250 | 4 | HG02258.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-591_1303-580d others(14): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57145491 | |||||
chr16:57145701
|
A | G | 9 | a0001c0001t0001g0096a0001c0001t0001g0112a0001c0001t0001g0113others(6): Show | 10 | HG01496.hp2 HG02818.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-384A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145701 | ||||||
chr16:57145764
|
C | T | 7 | a0001c0001t0003g0102a0001c0001t0003g0164a0001c0001t0003g0213others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-321C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145764 | ||||||
chr16:57145921
|
G | T | 1 | a0001c0001t0001g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1303-164G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145921 | ||||||
chr16:57145998
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0155others(2): Show | 5 | HG03471.hp1 HG03486.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-87C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145998 | ||||||
chr16:57146014
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0152a0001c0001t0001g0245others(5): Show | 10 | NA18952.hp2 NA18963.hp1 NA18993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-71T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57146014 | ||||||
chr16:57146351
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0247a0001c0001t0001g0304others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+30G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146351 | ||||||
chr16:57146352
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1539+31G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146352 | ||||||
chr16:57146555
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1539+234G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146555 | ||||||
chr16:57146580
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1539+259G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146580 | ||||||
chr16:57146624
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0252 | 2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1539+303G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146624 | ||||||
chr16:57146660
|
G | C | 7 | a0001c0001t0003g0102a0001c0001t0003g0164a0001c0001t0003g0213others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+339G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146660 | ||||||
chr16:57146805
|
G | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1539+484G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146805 | ||||||
chr16:57146862
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1539+541G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146862 | ||||||
chr16:57146922
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1539+601T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146922 | ||||||
chr16:57146972
|
G | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | NA18946.hp1 NA19062.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1540-579G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146972 | ||||||
chr16:57147222
|
C | T | 39 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0318others(36): Show | 41 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1540-329C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147222 | ||||||
chr16:57147239
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1540-312G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147239 | ||||||
chr16:57147251
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1540-300C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147251 | ||||||
chr16:57147330
|
T | TA | 3 | a0001c0001t0001g0075a0001c0001t0001g0246a0001c0001t0001g0249 | 3 | HG02630.hp2 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1540-220dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 57147330 | |||||
chr16:57147360
|
CAG | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0077a0001c0001t0001g0108others(13): Show | 17 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1540-190_1540-189d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147360 | ||||||
chr16:57147366
|
G | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0218a0001c0001t0001g0341 | 3 | HG01243.hp1 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1540-185G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147366 | ||||||
chr16:57147456
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1540-95G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147456 | ||||||
chr16:57147483
|
C | T | 1 | a0001c0002t0001g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1540-68C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147483 |