geneid | 8895 |
---|---|
ensemblid | ENSG00000085719.13 |
hgncid | 2316 |
symbol | CPNE3 |
name | copine 3 |
refseq_nuc | NM_003909.5 |
refseq_prot | NP_003900.1 |
ensembl_nuc | ENST00000517490.6 |
ensembl_prot | ENSP00000477590.1 |
mane_status | MANE Select |
chr | chr8 |
start | 86514435 |
end | 86561498 |
strand | + |
ver | v1.2 |
region | chr8:86514435-86561498 |
region5000 | chr8:86509435-86566498 |
regionname0 | CPNE3_chr8_86514435_86561498 |
regionname5000 | CPNE3_chr8_86509435_86566498 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 537 | 261 | 41 | 47 | 139 | 6 | 26 | 106 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002 | 0/0 | 537 | 38 | 16 | 9 | 3 | 2 | 8 | 3 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003 | 0/0 | 537 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004 | 0/0 | 537 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0005 | 0/0 | 537 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0006 | 0/0 | 537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0007 | 0/0 | 173 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0008 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0009 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0010 | 0/0 | 537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0011 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1614 | 214 | 22 | 42 | 122 | 5 | 21 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0002 | 0/0 | 1614 | 42 | 17 | 4 | 15 | 1 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0003 | 0/0 | 1614 | 26 | 9 | 5 | 3 | 2 | 7 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0004 | 0/0 | 1614 | 21 | 19 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0005 | 0/0 | 1614 | 12 | 7 | 4 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0006 | 0/0 | 1614 | 9 | 8 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0007 | 0/0 | 1614 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0008 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0009 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0010 | 0/0 | 1614 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0011 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0012 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0013 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0014 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0015 | 0/0 | 1571 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0016 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
c0017 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3245 | 77 | 5 | 22 | 42 | 2 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0002 | 0/0 | 3245 | 70 | 6 | 20 | 36 | 2 | 6 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0003 | 1/0 | 3244 | 53 | 1 | 2 | 40 | 2 | 7 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0004 | 0/0 | 3245 | 46 | 19 | 7 | 14 | 1 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0005 | 0/0 | 3245 | 38 | 19 | 8 | 3 | 1 | 7 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0006 | 0/0 | 3245 | 13 | 12 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0007 | 0/0 | 3247 | 9 | 8 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0008 | 0/0 | 3245 | 8 | 0 | 0 | 8 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0009 | 0/0 | 3245 | 6 | 5 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0010 | 0/0 | 3245 | 5 | 5 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0011 | 0/0 | 3245 | 4 | 4 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0012 | 0/0 | 3245 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0013 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0014 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0015 | 0/0 | 3244 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0016 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0017 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0018 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0019 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
t0020 | 0/0 | 3245 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1614 | 214 | 22 | 42 | 122 | 5 | 21 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002 | 0/0 | 1614 | 42 | 17 | 4 | 15 | 1 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0008 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0010 | 0/0 | 1614 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0017 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0003 | 0/0 | 1614 | 26 | 9 | 5 | 3 | 2 | 7 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0005 | 0/0 | 1614 | 12 | 7 | 4 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003c0004 | 0/0 | 1614 | 21 | 19 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004c0006 | 0/0 | 1614 | 9 | 8 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004c0013 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0005c0007 | 0/0 | 1614 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0006c0009 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0007c0011 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0008c0014 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0009c0015 | 0/0 | 1571 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0010c0016 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0011c0012 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4858 | 66 | 2 | 20 | 38 | 1 | 4 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0002 | 0/0 | 4858 | 50 | 2 | 17 | 23 | 2 | 6 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0003 | 1/0 | 4857 | 49 | 1 | 1 | 39 | 2 | 5 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0004 | 0/0 | 4858 | 26 | 7 | 3 | 14 | 0 | 2 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0006 | 0/0 | 4858 | 5 | 4 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0007 | 0/0 | 4860 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0008 | 0/0 | 4858 | 7 | 0 | 0 | 7 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0009 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0010 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0013 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0015 | 0/0 | 4857 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0016 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0017 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0018 | 0/0 | 4857 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0001t0020 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0001 | 0/0 | 4858 | 7 | 3 | 1 | 1 | 1 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0002 | 0/0 | 4858 | 15 | 0 | 2 | 13 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0003 | 0/0 | 4857 | 3 | 0 | 0 | 1 | 0 | 2 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0004 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0005 | 0/0 | 4858 | 2 | 0 | 0 | 0 | 0 | 2 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0006 | 0/0 | 4858 | 6 | 6 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0007 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0009 | 0/0 | 4858 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0010 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0014 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0002t0019 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0008t0002 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0008t0004 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0010t0001 | 0/0 | 4858 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0001c0017t0001 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0003t0002 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0003t0004 | 0/0 | 4858 | 5 | 0 | 1 | 0 | 1 | 3 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0003t0005 | 0/0 | 4858 | 20 | 9 | 3 | 3 | 1 | 4 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0005t0004 | 0/0 | 4858 | 3 | 1 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0002c0005t0005 | 0/0 | 4858 | 9 | 6 | 2 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003c0004t0004 | 0/0 | 4858 | 8 | 7 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003c0004t0006 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003c0004t0007 | 0/0 | 4860 | 5 | 4 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003c0004t0009 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0003c0004t0012 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004c0006t0002 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004c0006t0005 | 0/0 | 4858 | 4 | 3 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004c0006t0011 | 0/0 | 4858 | 4 | 4 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0004c0013t0005 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0005c0007t0010 | 0/0 | 4858 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0006c0009t0002 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0007c0011t0005 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0008c0014t0003 | 0/0 | 4857 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0009c0015t0001 | 0/0 | 4815 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0010c0016t0008 | 0/0 | 4858 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
a0011c0012t0005 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | copy fasta | chr8 | 86509435 | 86566498 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0013g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0017g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0018g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0001t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0009g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0002t0019g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0008t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0008t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0010t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0001c0017t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0003t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0002c0005t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0003c0004t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0006t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0004c0013t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0005c0007t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0005c0007t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0005c0007t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0006c0009t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0006c0009t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0007c0011t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0008c0014t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0009c0015t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0010c0016t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
a0011c0012t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0030 | EUR | GBR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0321 | EUR | GBR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00323 | hp1 | a0002 | c0003 | t0004 | g0086 | EUR | FIN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | FIN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00544 | hp1 | a0001 | c0010 | t0001 | g0049 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00609 | hp2 | a0009 | c0015 | t0001 | g0048 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00642 | hp2 | a0002 | c0003 | t0005 | g0182 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | CHS | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00733 | hp1 | a0011 | c0012 | t0005 | g0314 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00738 | hp2 | a0008 | c0014 | t0003 | g0006 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0289 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01069 | hp2 | a0002 | c0005 | t0004 | g0287 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01070 | hp1 | a0001 | c0002 | t0009 | g0315 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01071 | hp2 | a0002 | c0005 | t0004 | g0288 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01074 | hp1 | a0002 | c0003 | t0005 | g0214 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01081 | hp1 | a0003 | c0004 | t0007 | g0172 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01099 | hp2 | a0002 | c0003 | t0005 | g0143 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01109 | hp2 | a0002 | c0003 | t0002 | g0144 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0335 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01243 | hp1 | a0003 | c0004 | t0004 | g0179 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01255 | hp2 | a0007 | c0011 | t0005 | g0312 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01261 | hp1 | a0004 | c0006 | t0005 | g0281 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01433 | hp1 | a0002 | c0005 | t0005 | g0331 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01433 | hp2 | a0002 | c0005 | t0005 | g0291 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01884 | hp1 | a0003 | c0004 | t0004 | g0156 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01928 | hp1 | a0001 | c0017 | t0001 | g0105 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02004 | hp2 | a0002 | c0003 | t0004 | g0224 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02015 | hp1 | a0001 | c0001 | t0015 | g0263 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0300 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02055 | hp2 | a0003 | c0004 | t0004 | g0178 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0311 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0269 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02257 | hp1 | a0002 | c0005 | t0004 | g0333 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02257 | hp2 | a0003 | c0004 | t0007 | g0175 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02258 | hp1 | a0002 | c0005 | t0005 | g0320 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02258 | hp2 | a0003 | c0004 | t0007 | g0158 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02280 | hp1 | a0002 | c0003 | t0005 | g0020 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02572 | hp1 | a0004 | c0006 | t0002 | g0163 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02572 | hp2 | a0003 | c0004 | t0009 | g0188 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02615 | hp1 | a0001 | c0001 | t0020 | g0007 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02615 | hp2 | a0004 | c0006 | t0005 | g0161 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02622 | hp1 | a0002 | c0003 | t0005 | g0065 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02622 | hp2 | a0006 | c0009 | t0002 | g0066 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02647 | hp1 | a0003 | c0004 | t0006 | g0176 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02647 | hp2 | a0003 | c0004 | t0012 | g0283 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0316 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02698 | hp2 | a0002 | c0003 | t0005 | g0142 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02723 | hp2 | a0003 | c0004 | t0004 | g0165 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02809 | hp1 | a0001 | c0002 | t0007 | g0317 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02886 | hp1 | a0003 | c0004 | t0012 | g0282 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02895 | hp2 | a0002 | c0003 | t0005 | g0145 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02896 | hp1 | a0003 | c0004 | t0009 | g0186 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02897 | hp2 | a0003 | c0004 | t0009 | g0187 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02922 | hp1 | a0001 | c0002 | t0009 | g0295 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02922 | hp2 | a0001 | c0002 | t0006 | g0267 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02965 | hp1 | a0001 | c0002 | t0019 | g0294 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02965 | hp2 | a0002 | c0003 | t0005 | g0140 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0301 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02976 | hp2 | a0004 | c0013 | t0005 | g0164 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0324 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03017 | hp2 | a0002 | c0003 | t0005 | g0027 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0138 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03041 | hp2 | a0003 | c0004 | t0007 | g0168 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03098 | hp1 | a0001 | c0008 | t0004 | g0298 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03098 | hp2 | a0004 | c0006 | t0011 | g0155 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03130 | hp1 | a0002 | c0003 | t0005 | g0133 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03130 | hp2 | a0001 | c0002 | t0006 | g0292 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03139 | hp1 | a0004 | c0006 | t0011 | g0171 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03139 | hp2 | a0002 | c0003 | t0005 | g0131 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03195 | hp1 | a0004 | c0006 | t0005 | g0174 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03195 | hp2 | a0001 | c0002 | t0006 | g0268 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03209 | hp1 | a0003 | c0004 | t0004 | g0157 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03225 | hp1 | a0001 | c0002 | t0014 | g0296 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03225 | hp2 | a0002 | c0003 | t0005 | g0139 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03453 | hp1 | a0001 | c0008 | t0002 | g0297 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03453 | hp2 | a0001 | c0002 | t0010 | g0302 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03486 | hp1 | a0002 | c0003 | t0005 | g0080 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0035 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03490 | hp2 | a0002 | c0003 | t0004 | g0200 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03491 | hp1 | a0001 | c0001 | t0017 | g0212 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03491 | hp2 | a0001 | c0002 | t0005 | g0325 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03492 | hp1 | a0002 | c0003 | t0004 | g0216 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03492 | hp2 | a0001 | c0002 | t0005 | g0326 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03516 | hp1 | a0002 | c0003 | t0005 | g0083 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03516 | hp2 | a0005 | c0007 | t0010 | g0280 | AFR | ESN | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03540 | hp1 | a0002 | c0005 | t0005 | g0185 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03540 | hp2 | a0003 | c0004 | t0007 | g0173 | AFR | GWD | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03579 | hp1 | a0004 | c0006 | t0011 | g0154 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03669 | hp2 | a0002 | c0003 | t0005 | g0100 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0130 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03704 | hp1 | a0001 | c0001 | t0016 | g0060 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03927 | hp1 | a0002 | c0005 | t0005 | g0304 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG04115 | hp2 | a0002 | c0003 | t0005 | g0231 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0334 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG04199 | hp2 | a0001 | c0001 | t0018 | g0026 | SAS | STU | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18522 | hp1 | a0002 | c0005 | t0005 | g0003 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18906 | hp1 | a0003 | c0004 | t0012 | g0284 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18906 | hp2 | a0005 | c0007 | t0010 | g0279 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18953 | hp1 | a0001 | c0010 | t0001 | g0072 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18980 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18986 | hp1 | a0002 | c0003 | t0005 | g0095 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18987 | hp2 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18990 | hp2 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18992 | hp1 | a0002 | c0003 | t0005 | g0037 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18992 | hp2 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19003 | hp1 | a0001 | c0001 | t0008 | g0119 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19010 | hp1 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19030 | hp1 | a0004 | c0006 | t0005 | g0159 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0177 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19043 | hp2 | a0001 | c0002 | t0006 | g0270 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19058 | hp2 | a0001 | c0001 | t0008 | g0096 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19067 | hp2 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19072 | hp1 | a0002 | c0003 | t0005 | g0031 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19078 | hp2 | a0010 | c0016 | t0008 | g0079 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19240 | hp1 | a0003 | c0004 | t0006 | g0170 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0137 | AFR | YRI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20129 | hp1 | a0002 | c0005 | t0005 | g0003 | AFR | ASW | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20752 | hp2 | a0002 | c0003 | t0005 | g0215 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20905 | hp2 | a0002 | c0003 | t0004 | g0198 | SAS | GIH | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02109 | hp1 | a0006 | c0009 | t0002 | g0084 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02109 | hp2 | a0002 | c0005 | t0005 | g0327 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02486 | hp1 | a0004 | c0006 | t0011 | g0167 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02486 | hp2 | a0003 | c0004 | t0004 | g0162 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02559 | hp1 | a0001 | c0002 | t0006 | g0293 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG02559 | hp2 | a0002 | c0005 | t0005 | g0290 | AFR | ACB | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG03471 | hp2 | a0003 | c0004 | t0004 | g0166 | AFR | MSL | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG06807 | hp1 | a0001 | c0002 | t0004 | g0336 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20300 | hp1 | a0003 | c0004 | t0004 | g0169 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA21309 | hp1 | a0005 | c0007 | t0010 | g0278 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | LWK | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0271 | REF | REF | CPNE3_chr8_86509435_86566498 | CPNE3 | chr8 | 86509435 | 86566498 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:86531228
|
C | T | 1 | a0005 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
missense_variant&splice_region_variant | MODERATE | c.386C>T | p.Thr129Met | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/17 | 541/4857 | 386/1614 | 129/537 | chr8 | 86531228 | ||
chr8:86537625
|
G | A | 1 | a0007 | 1 | HG01255.hp2 | stop_gained | HIGH | c.522G>A | p.Trp174* | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/17 | 677/4857 | 522/1614 | 174/537 | chr8 | 86537625 | ||
chr8:86544740
|
G | A | 1 | a0008 | 1 | HG00738.hp2 | missense_variant&splice_region_variant | MODERATE | c.634G>A | p.Val212Met | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/17 | 789/4857 | 634/1614 | 212/537 | chr8 | 86544740 | ||
chr8:86546618
|
G | C | 2 | a0003a0004 | 31 | HG01081.hp1 HG01243.hp1 HG01261.hp1 others(28): Show |
missense_variant | MODERATE | c.756G>C | p.Glu252Asp | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/17 | 911/4857 | 756/1614 | 252/537 | chr8 | 86546618 | ||
chr8:86548326
|
A | G | 1 | a0011 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.905A>G | p.Asn302Ser | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/17 | 1060/4857 | 905/1614 | 302/537 | chr8 | 86548326 | ||
chr8:86548378
|
TAATGAGT others(36): Show |
T | 1 | a0009 | 1 | HG00609.hp2 | frameshift_variant | HIGH | c.960_1002delTGAGTAT others(36): Show |
p.Asn320fs | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/17 | 1115/4857 | 960/1614 | 320/537 | INFO_REALIGN_3_PRIME | chr8 | 86548378 | |
chr8:86554878
|
G | A | 1 | a0006 | 2 | HG02109.hp1 HG02622.hp2 |
missense_variant | MODERATE | c.1148G>A | p.Arg383Gln | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/17 | 1303/4857 | 1148/1614 | 383/537 | chr8 | 86554878 | ||
chr8:86554965
|
C | T | 5 | a0002a0004a0006others(2): Show | 52 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(49): Show |
missense_variant | MODERATE | c.1235C>T | p.Thr412Met | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/17 | 1390/4857 | 1235/1614 | 412/537 | chr8 | 86554965 | ||
chr8:86556265
|
G | A | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1418G>A | p.Ser473Asn | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/17 | 1573/4857 | 1418/1614 | 473/537 | chr8 | 86556265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:86528644
|
G | A | 5 | a0001c0002a0001c0008a0002c0005others(2): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
synonymous_variant | LOW | c.99G>A | p.Leu33Leu | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 3/17 | 254/4857 | 99/1614 | 33/537 | chr8 | 86528644 | ||
chr8:86540292
|
T | G | 1 | a0004c0013 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.591T>G | p.Ser197Ser | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/17 | 746/4857 | 591/1614 | 197/537 | chr8 | 86540292 | ||
chr8:86540310
|
C | T | 1 | a0001c0017 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.609C>T | p.Tyr203Tyr | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/17 | 764/4857 | 609/1614 | 203/537 | chr8 | 86540310 | ||
chr8:86544742
|
G | A | 1 | a0001c0008 | 2 | HG03098.hp1 HG03453.hp1 |
splice_region_variant&synonymous_variant | LOW | c.636G>A | p.Val212Val | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/17 | 791/4857 | 636/1614 | 212/537 | chr8 | 86544742 | ||
chr8:86554966
|
G | A | 1 | a0001c0010 | 2 | HG00544.hp1 NA18953.hp1 |
synonymous_variant | LOW | c.1236G>A | p.Thr412Thr | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/17 | 1391/4857 | 1236/1614 | 412/537 | chr8 | 86554966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:86514496
|
A | C | 1 | a0003c0004t0012 | 3 | HG02647.hp2 HG02886.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-94A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/17 | 14050 | chr8 | 86514496 | |||||
chr8:86558437
|
A | C | 14 | a0001c0001t0002a0001c0002t0002a0001c0002t0005others(11): Show | 112 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*27A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 27 | chr8 | 86558437 | |||||
chr8:86558500
|
C | T | 14 | a0001c0001t0002a0001c0002t0002a0001c0002t0005others(11): Show | 112 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 90 | chr8 | 86558500 | |||||
chr8:86558821
|
A | G | 14 | a0001c0001t0002a0001c0002t0002a0001c0002t0005others(11): Show | 112 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*411A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 411 | chr8 | 86558821 | |||||
chr8:86559016
|
G | A | 1 | a0001c0001t0013 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*606G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 606 | chr8 | 86559016 | |||||
chr8:86559024
|
A | G | 12 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(9): Show | 93 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*614A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 614 | chr8 | 86559024 | |||||
chr8:86559130
|
T | TAA | 3 | a0001c0001t0007a0001c0002t0007a0003c0004t0007 | 9 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*723dupAA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 724 | INFO_REALIGN_3_PRIME | chr8 | 86559130 | ||||
chr8:86559306
|
G | A | 8 | a0001c0001t0007a0001c0001t0010a0001c0002t0007others(5): Show | 18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 896 | chr8 | 86559306 | |||||
chr8:86559410
|
T | A | 8 | a0001c0001t0007a0001c0001t0010a0001c0002t0007others(5): Show | 18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1000 | chr8 | 86559410 | |||||
chr8:86559594
|
A | G | 10 | a0001c0001t0001a0001c0001t0008a0001c0001t0020others(7): Show | 91 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1184A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1184 | chr8 | 86559594 | |||||
chr8:86559689
|
G | A | 1 | a0001c0002t0019 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1279 | chr8 | 86559689 | |||||
chr8:86559921
|
G | A | 1 | a0001c0001t0020 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1511G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1511 | chr8 | 86559921 | |||||
chr8:86560238
|
C | A | 1 | a0001c0001t0015 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1828 | chr8 | 86560238 | |||||
chr8:86560332
|
C | T | 1 | a0001c0001t0018 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 1922 | chr8 | 86560332 | |||||
chr8:86560435
|
C | T | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(14): Show | 138 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*2025C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2025 | chr8 | 86560435 | |||||
chr8:86560437
|
A | T | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(40): Show | 282 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2027A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2027 | chr8 | 86560437 | |||||
chr8:86560473
|
G | A | 1 | a0001c0001t0016 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2063G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2063 | chr8 | 86560473 | |||||
chr8:86560606
|
T | TA | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(40): Show | 282 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2200dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2201 | INFO_REALIGN_3_PRIME | chr8 | 86560606 | ||||
chr8:86560675
|
A | G | 2 | a0001c0001t0008a0010c0016t0008 | 8 | NA18980.hp1 NA18987.hp2 NA18990.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2265A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2265 | chr8 | 86560675 | |||||
chr8:86560771
|
C | T | 10 | a0001c0001t0007a0001c0001t0009a0001c0001t0010others(7): Show | 23 | HG01070.hp1 HG01081.hp1 HG02257.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2361 | chr8 | 86560771 | |||||
chr8:86560840
|
G | A | 1 | a0001c0001t0017 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2430 | chr8 | 86560840 | |||||
chr8:86560892
|
C | T | 7 | a0001c0002t0005a0002c0003t0005a0002c0005t0005others(4): Show | 38 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2482C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 2482 | chr8 | 86560892 | |||||
chr8:86561416
|
G | C | 26 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | 144 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3006G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 17/17 | 3006 | chr8 | 86561416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:86514562
|
G | A | 127 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(124): Show | 127 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49+21G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514562 | ||||||
chr8:86514595
|
C | G | 53 | a0001c0001t0002g0286a0001c0002t0001g0303a0001c0002t0001g0310others(50): Show | 54 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-49+54C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514595 | ||||||
chr8:86514740
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+199G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514740 | ||||||
chr8:86514820
|
C | T | 1 | a0001c0001t0013g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-49+279C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514820 | ||||||
chr8:86514850
|
G | T | 1 | a0001c0002t0002g0337 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-49+309G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514850 | ||||||
chr8:86514952
|
G | A | 15 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49+411G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86514952 | ||||||
chr8:86515176
|
C | T | 3 | a0003c0004t0012g0282a0003c0004t0012g0283a0003c0004t0012g0284 | 3 | HG02647.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-48-286C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86515176 | ||||||
chr8:86515335
|
G | T | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-48-127G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 1/16 | chr8 | 86515335 | ||||||
chr8:86515571
|
A | G | 1 | a0004c0006t0005g0281 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-11+72A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515571 | ||||||
chr8:86515605
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+106C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515605 | ||||||
chr8:86515785
|
G | A | 7 | a0001c0001t0001g0146a0001c0001t0002g0147a0001c0001t0002g0148others(4): Show | 7 | HG00558.hp1 NA18950.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+286G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515785 | ||||||
chr8:86515833
|
A | G | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+334A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86515833 | ||||||
chr8:86516190
|
C | T | 38 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(35): Show | 39 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-11+691C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516190 | ||||||
chr8:86516192
|
G | T | 1 | a0001c0002t0002g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-11+693G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516192 | ||||||
chr8:86516207
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-11+708A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516207 | ||||||
chr8:86516216
|
G | T | 3 | a0001c0001t0001g0275a0001c0001t0003g0276a0001c0001t0003g0277 | 3 | NA19007.hp1 NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-11+717G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516216 | ||||||
chr8:86516279
|
G | T | 4 | a0001c0001t0002g0274a0001c0001t0004g0002a0001c0001t0004g0272others(1): Show | 5 | NA18965.hp1 NA18984.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+780G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516279 | ||||||
chr8:86516282
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-11+783C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516282 | ||||||
chr8:86516479
|
G | C | 1 | a0001c0002t0004g0300 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+980G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516479 | ||||||
chr8:86516521
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-11+1022G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516521 | ||||||
chr8:86516630
|
T | A | 136 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(133): Show | 138 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-11+1131T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516630 | ||||||
chr8:86516915
|
G | A | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+1416G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86516915 | ||||||
chr8:86517069
|
A | C | 151 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(148): Show | 153 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-11+1570A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517069 | ||||||
chr8:86517080
|
T | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1581T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517080 | ||||||
chr8:86517127
|
G | A | 328 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.-11+1628G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517127 | ||||||
chr8:86517269
|
A | C | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1770A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517269 | ||||||
chr8:86517284
|
A | T | 34 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0094others(31): Show | 34 | HG00597.hp2 HG00673.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+1785A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517284 | ||||||
chr8:86517288
|
A | G | 1 | a0002c0003t0004g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11+1789A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517288 | ||||||
chr8:86517304
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-11+1805T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517304 | ||||||
chr8:86517431
|
C | A | 4 | a0001c0002t0006g0292a0001c0002t0006g0293a0001c0002t0009g0295others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+1932C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517431 | ||||||
chr8:86517435
|
C | G | 1 | a0001c0001t0002g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-11+1936C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517435 | ||||||
chr8:86517828
|
A | G | 94 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(91): Show | 96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-11+2329A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517828 | ||||||
chr8:86517843
|
G | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2344G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517843 | ||||||
chr8:86517972
|
A | G | 3 | a0003c0004t0009g0186a0003c0004t0009g0187a0003c0004t0009g0188 | 3 | HG02572.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11+2473A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86517972 | ||||||
chr8:86518137
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-11+2638C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518137 | ||||||
chr8:86518201
|
G | A | 2 | a0004c0006t0011g0154a0004c0006t0011g0155 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-11+2702G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518201 | ||||||
chr8:86518242
|
G | A | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2743G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518242 | ||||||
chr8:86518256
|
C | T | 1 | a0002c0003t0005g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+2757C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518256 | ||||||
chr8:86518257
|
A | G | 209 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(206): Show | 212 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-11+2758A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518257 | ||||||
chr8:86518433
|
T | C | 2 | a0003c0004t0004g0156a0003c0004t0004g0157 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-11+2934T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518433 | ||||||
chr8:86518518
|
G | A | 2 | a0001c0001t0002g0005a0008c0014t0003g0006 | 2 | HG00738.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-11+3019G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518518 | ||||||
chr8:86518563
|
G | T | 53 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(50): Show | 54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+3064G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518563 | ||||||
chr8:86518565
|
T | C | 53 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(50): Show | 54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+3066T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518565 | ||||||
chr8:86518732
|
A | G | 1 | a0002c0003t0002g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+3233A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518732 | ||||||
chr8:86518762
|
T | A | 2 | a0002c0003t0005g0131a0002c0003t0005g0145 | 2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-11+3263T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518762 | ||||||
chr8:86518762
|
TA | T | 54 | a0001c0001t0008g0119a0001c0002t0001g0303a0001c0002t0001g0310others(51): Show | 55 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.-11+3272delA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86518762 | |||||
chr8:86518763
|
A | T | 10 | a0001c0001t0001g0082a0001c0001t0002g0265a0001c0001t0003g0081others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+3264A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86518763 | ||||||
chr8:86519052
|
G | A | 1 | a0001c0002t0002g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-11+3553G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519052 | ||||||
chr8:86519119
|
A | G | 15 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+3620A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519119 | ||||||
chr8:86519322
|
T | C | 4 | a0001c0002t0006g0292a0001c0002t0006g0293a0001c0002t0009g0295others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+3823T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519322 | ||||||
chr8:86519504
|
T | G | 1 | a0001c0001t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+4005T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519504 | ||||||
chr8:86519637
|
G | C | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+4138G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519637 | ||||||
chr8:86519691
|
G | C | 1 | a0001c0001t0020g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11+4192G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519691 | ||||||
chr8:86519779
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-11+4280T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519779 | ||||||
chr8:86519799
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0015g0263 | 2 | HG02015.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-11+4300C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519799 | ||||||
chr8:86519816
|
C | T | 53 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(50): Show | 54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+4317C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519816 | ||||||
chr8:86519991
|
C | T | 1 | a0006c0009t0002g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-11+4492C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86519991 | ||||||
chr8:86520001
|
C | T | 1 | a0010c0016t0008g0079 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-11+4502C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520001 | ||||||
chr8:86520002
|
G | A | 53 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(50): Show | 54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-11+4503G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520002 | ||||||
chr8:86520060
|
T | C | 40 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(37): Show | 41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-11+4561T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520060 | ||||||
chr8:86520140
|
C | CCACTTCC others(197): Show |
5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+4644_-11+4847d others(206): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520140 | |||||
chr8:86520270
|
C | T | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-11+4771C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520270 | ||||||
chr8:86520331
|
G | A | 1 | a0001c0002t0014g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+4832G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520331 | ||||||
chr8:86520398
|
A | T | 1 | a0001c0001t0004g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+4899A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520398 | ||||||
chr8:86520487
|
G | A | 1 | a0001c0002t0004g0301 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+4988G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520487 | ||||||
chr8:86520504
|
C | G | 40 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(37): Show | 41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-11+5005C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520504 | ||||||
chr8:86520532
|
C | T | 1 | a0001c0001t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+5033C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520532 | ||||||
chr8:86520554
|
C | CAA | 39 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(36): Show | 40 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-11+5066_-11+5067d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520554 | |||||
chr8:86520593
|
C | T | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5094C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520593 | ||||||
chr8:86520608
|
G | C | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+5109G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520608 | ||||||
chr8:86520662
|
C | CT | 191 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(188): Show | 194 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-11+5178dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520662 | |||||
chr8:86520662
|
C | CTT | 14 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0261others(11): Show | 14 | HG00642.hp2 HG01109.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11+5177_-11+5178d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86520662 | |||||
chr8:86520959
|
G | A | 9 | a0001c0001t0001g0146a0001c0001t0002g0004a0001c0001t0002g0147others(6): Show | 9 | HG00438.hp2 HG00558.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+5460G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86520959 | ||||||
chr8:86521165
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-11+5666C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521165 | ||||||
chr8:86521289
|
T | C | 1 | a0001c0001t0003g0009 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-11+5790T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521289 | ||||||
chr8:86521537
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-11+6038G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521537 | ||||||
chr8:86521875
|
G | A | 1 | a0001c0002t0006g0292 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-11+6376G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521875 | ||||||
chr8:86521973
|
T | TA | 7 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194others(4): Show | 7 | HG00642.hp1 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+6483dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86521973 | |||||
chr8:86521982
|
A | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+6483A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86521982 | ||||||
chr8:86522123
|
C | T | 53 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(50): Show | 54 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-10-6413C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522123 | ||||||
chr8:86522201
|
T | G | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-6335T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522201 | ||||||
chr8:86522274
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10-6262G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522274 | ||||||
chr8:86522302
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-10-6234T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522302 | ||||||
chr8:86522306
|
C | T | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6230C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522306 | ||||||
chr8:86522442
|
T | C | 1 | a0002c0003t0004g0198 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-10-6094T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522442 | ||||||
chr8:86522462
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-10-6074A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522462 | ||||||
chr8:86522500
|
G | A | 1 | a0001c0002t0004g0300 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-6036G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522500 | ||||||
chr8:86522516
|
G | GGATTTAC | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-6019_-10-6013d others(9): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522516 | |||||
chr8:86522543
|
C | T | 3 | a0001c0001t0002g0260a0001c0001t0003g0258a0001c0001t0003g0259 | 3 | NA18953.hp2 NA18954.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-10-5993C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522543 | ||||||
chr8:86522544
|
G | A | 1 | a0003c0004t0007g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10-5992G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522544 | ||||||
chr8:86522548
|
C | CT | 45 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071others(42): Show | 45 | HG00673.hp1 HG00735.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.-10-5959dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
C | CTTTT | 30 | a0001c0002t0001g0310a0001c0002t0001g0319a0001c0002t0001g0321others(27): Show | 31 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-10-5962_-10-5959d others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
C | CTTTTT | 10 | a0001c0002t0002g0299a0001c0002t0002g0330a0001c0002t0002g0332others(7): Show | 10 | HG01175.hp2 HG01433.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-5963_-10-5959d others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0002g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-5968_-10-5959d others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
C | CTTTTTTT others(4): Show |
1 | a0002c0005t0005g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-10-5969_-10-5959d others(13): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
C | CTTTTTTT others(6): Show |
1 | a0002c0005t0005g0291 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10-5971_-10-5959d others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
CT | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-5959delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-10-5968_-10-5959d others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
CTTTTTTT others(4): Show |
C | 91 | a0001c0001t0001g0189a0001c0001t0001g0205a0001c0001t0001g0207others(88): Show | 93 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-10-5969_-10-5959d others(13): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522548
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0146a0001c0001t0003g0199a0002c0003t0004g0200 | 3 | HG00323.hp2 HG03490.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-10-5970_-10-5959d others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86522548 | |||||
chr8:86522641
|
T | A | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.-10-5895T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522641 | ||||||
chr8:86522762
|
A | G | 1 | a0001c0001t0002g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-10-5774A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86522762 | ||||||
chr8:86523018
|
G | A | 60 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(57): Show | 61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-10-5518G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523018 | ||||||
chr8:86523105
|
A | C | 1 | a0001c0001t0002g0191 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-10-5431A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523105 | ||||||
chr8:86523157
|
C | T | 55 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(52): Show | 55 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.-10-5379C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523157 | ||||||
chr8:86523345
|
G | A | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.-10-5191G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523345 | ||||||
chr8:86523349
|
A | T | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5187A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523349 | ||||||
chr8:86523493
|
A | C | 1 | a0001c0001t0002g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-10-5043A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523493 | ||||||
chr8:86523589
|
G | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-4947G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523589 | ||||||
chr8:86523641
|
A | C | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-4895A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523641 | ||||||
chr8:86523688
|
T | C | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.-10-4848T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523688 | ||||||
chr8:86523710
|
C | T | 4 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-4826C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86523710 | ||||||
chr8:86524383
|
T | A | 1 | a0001c0002t0014g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-4153T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524383 | ||||||
chr8:86524410
|
T | G | 60 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(57): Show | 61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-10-4126T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524410 | ||||||
chr8:86524656
|
G | A | 1 | a0004c0006t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-3880G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524656 | ||||||
chr8:86524674
|
C | T | 16 | a0001c0001t0001g0242a0001c0001t0001g0248a0001c0001t0002g0251others(13): Show | 16 | HG00597.hp1 HG00673.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-3862C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524674 | ||||||
chr8:86524681
|
A | AT | 63 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0075others(60): Show | 63 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-10-3835dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | |||||
chr8:86524681
|
A | ATT | 50 | a0001c0001t0001g0107a0001c0001t0001g0181a0001c0001t0001g0183others(47): Show | 51 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-3836_-10-3835d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | |||||
chr8:86524681
|
A | ATTT | 9 | a0001c0001t0002g0193a0001c0001t0010g0177a0001c0002t0002g0289others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-3837_-10-3835d others(5): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | |||||
chr8:86524681
|
A | ATTTTT | 74 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0209others(71): Show | 76 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-10-3839_-10-3835d others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | |||||
chr8:86524681
|
A | ATTTTTT | 17 | a0001c0001t0001g0189a0001c0001t0001g0235a0001c0001t0001g0261others(14): Show | 17 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-3840_-10-3835d others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524681 | |||||
chr8:86524742
|
G | A | 150 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(147): Show | 152 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-10-3794G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524742 | ||||||
chr8:86524848
|
T | TTTTCTTT others(1): Show |
144 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(141): Show | 146 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.-10-3672_-10-3665d others(10): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(5): Show |
8 | a0001c0001t0001g0264a0001c0001t0003g0199a0001c0001t0004g0201others(5): Show | 8 | HG00323.hp2 HG02015.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-3676_-10-3665d others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(21): Show |
4 | a0001c0002t0002g0328a0001c0002t0003g0334a0001c0008t0004g0298others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(30): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(25): Show |
13 | a0001c0002t0001g0319a0001c0002t0001g0321a0001c0002t0001g0322others(10): Show | 14 | HG00099.hp2 HG01175.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(34): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(29): Show |
17 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0002g0309others(14): Show | 17 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(38): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(33): Show |
5 | a0001c0002t0002g0306a0001c0002t0002g0307a0001c0002t0006g0269others(2): Show | 5 | HG01433.hp1 HG02083.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(42): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(37): Show |
6 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0293others(3): Show | 6 | HG02559.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(46): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(41): Show |
3 | a0001c0002t0004g0300a0001c0002t0004g0336a0001c0002t0006g0292 | 3 | HG02055.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(50): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524848
|
T | TTTTCTTT others(45): Show |
2 | a0001c0002t0010g0302a0001c0008t0002g0297 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-10-3665_-10-3664i others(54): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524848 | |||||
chr8:86524853
|
T | TTTCTTTC others(82): Show |
1 | a0002c0005t0004g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-10-3664_-10-3663i others(91): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | |||||
chr8:86524853
|
T | TTTCTTTC others(73): Show |
2 | a0002c0005t0005g0290a0002c0005t0005g0291 | 2 | HG01433.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-10-3662_-10-3661i others(82): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | |||||
chr8:86524853
|
T | TTTCTTTC others(81): Show |
1 | a0002c0005t0004g0288 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-10-3662_-10-3661i others(90): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | |||||
chr8:86524853
|
T | TTTCTTTC others(85): Show |
1 | a0001c0002t0002g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-3662_-10-3661i others(94): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524853 | |||||
chr8:86524869
|
T | TTTCTTTC others(31): Show |
1 | a0001c0002t0002g0305 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-10-3665_-10-3664i others(40): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524869 | |||||
chr8:86524870
|
T | TTCTTTCT others(31): Show |
1 | a0001c0002t0002g0330 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-10-3665_-10-3664i others(40): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86524870 | |||||
chr8:86524894
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG01192.hp1 HG01496.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-3642C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86524894 | ||||||
chr8:86525044
|
G | A | 261 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0094others(258): Show | 264 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(261): Show |
intron_variant | MODIFIER | c.-10-3492G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525044 | ||||||
chr8:86525128
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0003g0239a0001c0001t0003g0240others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3408T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525128 | ||||||
chr8:86525147
|
G | A | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-3389G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525147 | ||||||
chr8:86525228
|
C | T | 1 | a0001c0001t0003g0277 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-10-3308C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525228 | ||||||
chr8:86525351
|
A | T | 3 | a0001c0001t0001g0126a0001c0001t0003g0125a0001c0001t0003g0127 | 3 | HG02056.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-10-3185A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525351 | ||||||
chr8:86525363
|
A | G | 5 | a0001c0002t0006g0292a0001c0002t0006g0293a0001c0002t0009g0295others(2): Show | 5 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3173A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525363 | ||||||
chr8:86525445
|
G | A | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3091G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525445 | ||||||
chr8:86525480
|
A | T | 95 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(92): Show | 97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-3056A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525480 | ||||||
chr8:86525659
|
T | C | 1 | a0003c0004t0006g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10-2877T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525659 | ||||||
chr8:86525753
|
G | A | 2 | a0003c0004t0004g0162a0004c0006t0005g0161 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-10-2783G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525753 | ||||||
chr8:86525778
|
T | C | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-2758T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86525778 | ||||||
chr8:86526184
|
C | T | 95 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(92): Show | 97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-2352C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526184 | ||||||
chr8:86526227
|
C | CA | 6 | a0001c0001t0001g0091a0001c0001t0001g0108a0001c0001t0002g0121others(3): Show | 6 | HG04199.hp2 NA19010.hp1 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2296dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86526227 | |||||
chr8:86526241
|
T | C | 2 | a0001c0001t0002g0028a0002c0003t0005g0027 | 2 | HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-10-2295T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526241 | ||||||
chr8:86526503
|
TTTTG | T | 40 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(37): Show | 40 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10-2021_-10-2018d others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86526503 | |||||
chr8:86526718
|
A | T | 9 | a0003c0004t0004g0179a0003c0004t0007g0158a0003c0004t0007g0172others(6): Show | 9 | HG01081.hp1 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-1818A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526718 | ||||||
chr8:86526764
|
G | A | 5 | a0001c0001t0002g0005a0001c0001t0003g0029a0001c0001t0003g0030others(2): Show | 5 | HG00099.hp1 HG00738.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1772G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526764 | ||||||
chr8:86526827
|
C | T | 1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-1709C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526827 | ||||||
chr8:86526904
|
T | A | 15 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-1632T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86526904 | ||||||
chr8:86527100
|
A | C | 3 | a0001c0001t0003g0081a0002c0003t0005g0083a0006c0009t0002g0084 | 3 | HG02109.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-1436A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527100 | ||||||
chr8:86527162
|
G | C | 1 | a0001c0001t0008g0089 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-10-1374G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527162 | ||||||
chr8:86527217
|
G | C | 1 | a0001c0001t0002g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10-1319G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527217 | ||||||
chr8:86527242
|
C | T | 2 | a0003c0004t0007g0158a0003c0004t0007g0175 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-10-1294C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527242 | ||||||
chr8:86527472
|
G | A | 2 | a0001c0001t0003g0202a0001c0001t0003g0203 | 2 | HG00544.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-10-1064G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527472 | ||||||
chr8:86527524
|
A | G | 33 | a0001c0001t0004g0160a0001c0001t0010g0177a0003c0004t0004g0156others(30): Show | 33 | HG01069.hp1 HG01081.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-10-1012A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527524 | ||||||
chr8:86527604
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10-932T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527604 | ||||||
chr8:86527639
|
T | C | 95 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(92): Show | 97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-897T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527639 | ||||||
chr8:86527711
|
A | G | 14 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(11): Show | 14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10-825A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527711 | ||||||
chr8:86527798
|
A | T | 94 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(91): Show | 96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-10-738A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527798 | ||||||
chr8:86527831
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-10-705A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527831 | ||||||
chr8:86527891
|
A | G | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-645A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527891 | ||||||
chr8:86527946
|
A | AT | 19 | a0001c0001t0001g0064a0001c0001t0001g0073a0001c0001t0002g0059others(16): Show | 19 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-565dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATT | 10 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(7): Show | 10 | HG00642.hp2 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-566_-10-565dup others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(2): Show |
42 | a0001c0001t0001g0146a0001c0001t0001g0205a0001c0001t0001g0207others(39): Show | 43 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-10-573_-10-565dup others(9): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(3): Show |
27 | a0001c0001t0001g0189a0001c0001t0001g0217a0001c0001t0001g0226others(24): Show | 28 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-10-574_-10-565dup others(10): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(4): Show |
17 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(14): Show | 17 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-575_-10-565dup others(11): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(5): Show |
7 | a0001c0001t0001g0242a0001c0001t0002g0236a0001c0001t0003g0153others(4): Show | 7 | HG00438.hp1 HG00741.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-576_-10-565dup others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(6): Show |
6 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0001t0004g0238others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-577_-10-565dup others(13): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(7): Show |
4 | a0001c0001t0004g0132a0001c0001t0007g0138a0002c0003t0005g0131others(1): Show | 4 | HG01099.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-578_-10-565dup others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(8): Show |
2 | a0002c0003t0005g0139a0002c0003t0005g0140 | 2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-10-579_-10-565dup others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0002g0141a0002c0003t0002g0144 | 2 | HG01109.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-10-580_-10-565dup others(16): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(10): Show |
1 | a0002c0003t0005g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-10-581_-10-565dup others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(13): Show |
3 | a0003c0004t0004g0156a0003c0004t0012g0283a0004c0013t0005g0164 | 3 | HG01884.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-10-584_-10-565dup others(20): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(14): Show |
6 | a0003c0004t0004g0157a0003c0004t0004g0165a0003c0004t0004g0179others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-585_-10-565dup others(21): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(15): Show |
3 | a0003c0004t0004g0162a0003c0004t0004g0178a0004c0006t0005g0161 | 3 | HG02055.hp2 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-10-586_-10-565dup others(22): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0010g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-587_-10-565dup others(23): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(17): Show |
1 | a0003c0004t0004g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-588_-10-565dup others(24): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(19): Show |
2 | a0003c0004t0007g0168a0004c0006t0011g0167 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-10-565_-10-564ins others(26): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(20): Show |
2 | a0003c0004t0004g0169a0004c0006t0011g0154 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-10-565_-10-564ins others(27): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(21): Show |
4 | a0003c0004t0006g0170a0004c0006t0005g0281a0004c0006t0011g0155others(1): Show | 4 | HG01261.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-565_-10-564ins others(28): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
A | ATTTTTTT others(22): Show |
1 | a0004c0006t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-565_-10-564ins others(29): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
AT | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0087a0001c0001t0001g0091others(47): Show | 50 | HG00323.hp1 HG00597.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10-565delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527946
|
ATT | A | 6 | a0001c0001t0002g0093a0001c0001t0003g0092a0001c0001t0006g0011others(3): Show | 6 | HG01167.hp2 HG02615.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-566_-10-565del others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr8 | 86527946 | |||||
chr8:86527974
|
A | G | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-562A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86527974 | ||||||
chr8:86528186
|
G | A | 1 | a0001c0001t0004g0033 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-10-350G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86528186 | ||||||
chr8:86528210
|
A | G | 1 | a0001c0002t0003g0334 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-10-326A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 2/16 | chr8 | 86528210 | ||||||
chr8:86528745
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+68A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 3/16 | chr8 | 86528745 | ||||||
chr8:86528918
|
C | T | 5 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-27C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 3/16 | chr8 | 86528918 | ||||||
chr8:86529225
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.312+101C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529225 | ||||||
chr8:86529274
|
C | T | 3 | a0001c0001t0002g0121a0001c0001t0003g0120a0001c0001t0003g0124 | 3 | NA19062.hp2 NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.312+150C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529274 | ||||||
chr8:86529415
|
C | T | 4 | a0001c0001t0002g0274a0001c0001t0004g0002a0001c0001t0004g0272others(1): Show | 5 | NA18965.hp1 NA18984.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+291C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529415 | ||||||
chr8:86529618
|
G | C | 1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.312+494G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529618 | ||||||
chr8:86529847
|
A | G | 2 | a0001c0001t0001g0008a0001c0010t0001g0072 | 2 | NA18946.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.312+723A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529847 | ||||||
chr8:86529930
|
T | C | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.312+806T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529930 | ||||||
chr8:86529955
|
A | G | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.312+831A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86529955 | ||||||
chr8:86530058
|
C | T | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.312+934C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530058 | ||||||
chr8:86530089
|
A | G | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.312+965A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530089 | ||||||
chr8:86530170
|
CT | C | 206 | a0001c0001t0001g0034a0001c0001t0001g0146a0001c0001t0001g0181others(203): Show | 209 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.313-968delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86530170 | |||||
chr8:86530690
|
ATT | A | 150 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(147): Show | 152 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.313-448_313-447del others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86530690 | |||||
chr8:86530690
|
ATTT | A | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.313-449_313-447del others(3): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86530690 | |||||
chr8:86530736
|
G | A | 7 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(4): Show | 7 | HG00642.hp2 NA18960.hp2 NA19007.hp1 others(4): Show |
intron_variant | MODIFIER | c.313-419G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530736 | ||||||
chr8:86530740
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.313-415G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530740 | ||||||
chr8:86530796
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.313-359A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530796 | ||||||
chr8:86530938
|
C | T | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.313-217C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530938 | ||||||
chr8:86530991
|
T | C | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.313-164T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86530991 | ||||||
chr8:86531031
|
G | GAATGTTT others(8): Show |
2 | a0001c0001t0001g0183a0001c0001t0003g0184 | 2 | NA18960.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.313-119_313-105dup others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr8 | 86531031 | |||||
chr8:86531052
|
C | T | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.313-103C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 4/16 | chr8 | 86531052 | ||||||
chr8:86531279
|
A | T | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.387+50A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531279 | ||||||
chr8:86531551
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.387+322G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531551 | ||||||
chr8:86531643
|
T | C | 1 | a0001c0001t0006g0011 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.387+414T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531643 | ||||||
chr8:86531645
|
GTCAATGA others(19): Show |
G | 48 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(45): Show | 49 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.387+420_387+445del others(26): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr8 | 86531645 | |||||
chr8:86531946
|
G | A | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.388-563G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531946 | ||||||
chr8:86531962
|
G | A | 334 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(331): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.388-547G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86531962 | ||||||
chr8:86532012
|
G | A | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-497G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86532012 | ||||||
chr8:86532240
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | NA18950.hp2 NA18964.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-269C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 5/16 | chr8 | 86532240 | ||||||
chr8:86532604
|
A | G | 52 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(49): Show | 53 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.459+24A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532604 | ||||||
chr8:86532798
|
T | TAAGAGAG others(339): Show |
2 | a0001c0002t0005g0325a0001c0002t0005g0326 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.459+232_459+233ins others(346): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86532798 | |||||
chr8:86532814
|
T | C | 1 | a0002c0005t0005g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.459+234T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532814 | ||||||
chr8:86532842
|
A | T | 1 | a0001c0001t0015g0263 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.459+262A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532842 | ||||||
chr8:86532870
|
G | A | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.459+290G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532870 | ||||||
chr8:86532931
|
A | C | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+351A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86532931 | ||||||
chr8:86533024
|
T | TTATC | 104 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(101): Show | 104 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.459+486_459+489dup others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | |||||
chr8:86533024
|
T | TTATCTAT others(1): Show |
48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0068others(45): Show | 48 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.459+482_459+489dup others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | |||||
chr8:86533024
|
T | TTATCTAT others(5): Show |
5 | a0001c0002t0002g0328a0001c0002t0003g0308a0001c0010t0001g0072others(2): Show | 6 | HG02258.hp1 NA18522.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+478_459+489dup others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | |||||
chr8:86533024
|
TTATC | T | 12 | a0001c0001t0001g0207a0001c0001t0002g0122a0001c0001t0002g0123others(9): Show | 12 | HG00099.hp1 HG01496.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+486_459+489del others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | |||||
chr8:86533024
|
TTATCTAT others(5): Show |
T | 13 | a0001c0001t0001g0189a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG00558.hp2 HG00609.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+478_459+489del others(12): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | |||||
chr8:86533024
|
TTATCTAT others(9): Show |
T | 12 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0274others(9): Show | 14 | HG01975.hp2 HG02300.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.459+474_459+489del others(16): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533024 | |||||
chr8:86533054
|
A | ATCTC | 6 | a0003c0004t0004g0169a0003c0004t0007g0168a0004c0006t0011g0154others(3): Show | 6 | HG02486.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+477_459+478ins others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533054 | |||||
chr8:86533308
|
C | T | 3 | a0003c0004t0012g0282a0003c0004t0012g0283a0003c0004t0012g0284 | 3 | HG02647.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.459+728C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533308 | ||||||
chr8:86533324
|
C | T | 1 | a0002c0003t0005g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.459+744C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533324 | ||||||
chr8:86533501
|
T | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+921T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533501 | ||||||
chr8:86533825
|
C | T | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+1245C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533825 | ||||||
chr8:86533878
|
CTCCCTCC others(2): Show |
C | 43 | a0001c0001t0001g0069a0001c0001t0001g0087a0001c0001t0001g0091others(40): Show | 43 | HG00597.hp2 HG00673.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.459+1302_459+1310d others(11): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86533878 | |||||
chr8:86533884
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+1304C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533884 | ||||||
chr8:86533970
|
C | A | 1 | a0003c0004t0004g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459+1390C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86533970 | ||||||
chr8:86534089
|
C | T | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.459+1509C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534089 | ||||||
chr8:86534152
|
G | A | 14 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(11): Show | 14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.459+1572G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534152 | ||||||
chr8:86534323
|
A | T | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.459+1743A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534323 | ||||||
chr8:86534633
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.459+2053C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534633 | ||||||
chr8:86534784
|
G | A | 1 | a0001c0001t0013g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.459+2204G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534784 | ||||||
chr8:86534800
|
T | C | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.459+2220T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534800 | ||||||
chr8:86534806
|
A | G | 3 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0250 | 3 | NA18941.hp2 NA18987.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.459+2226A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534806 | ||||||
chr8:86534823
|
C | A | 95 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(92): Show | 97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.459+2243C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86534823 | ||||||
chr8:86534900
|
TTG | T | 5 | a0001c0001t0004g0132a0001c0001t0004g0135a0001c0001t0004g0136others(2): Show | 5 | HG02965.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+2326_459+2327d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86534900 | |||||
chr8:86535045
|
A | G | 60 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(57): Show | 61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.459+2465A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535045 | ||||||
chr8:86535073
|
T | TC | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-2489dupC | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86535073 | |||||
chr8:86535320
|
C | CT | 95 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(92): Show | 97 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.460-2229dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr8 | 86535320 | |||||
chr8:86535396
|
G | A | 2 | a0001c0001t0004g0012a0001c0001t0004g0055 | 2 | NA18943.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.460-2167G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535396 | ||||||
chr8:86535597
|
G | C | 3 | a0001c0002t0002g0305a0001c0002t0002g0309a0001c0002t0002g0330 | 3 | NA18941.hp1 NA19067.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.460-1966G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535597 | ||||||
chr8:86535607
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-1956A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535607 | ||||||
chr8:86535674
|
A | T | 1 | a0004c0006t0005g0281 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.460-1889A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535674 | ||||||
chr8:86535680
|
A | T | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-1883A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86535680 | ||||||
chr8:86536029
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.460-1534A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536029 | ||||||
chr8:86536341
|
A | T | 3 | a0001c0001t0001g0275a0001c0001t0003g0276a0001c0001t0003g0277 | 3 | NA19007.hp1 NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.460-1222A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536341 | ||||||
chr8:86536565
|
T | A | 40 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(37): Show | 40 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.460-998T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536565 | ||||||
chr8:86536709
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.460-854A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536709 | ||||||
chr8:86536725
|
C | G | 60 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(57): Show | 61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.460-838C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536725 | ||||||
chr8:86536761
|
T | C | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.460-802T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536761 | ||||||
chr8:86536781
|
T | A | 1 | a0001c0001t0003g0029 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.460-782T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536781 | ||||||
chr8:86536825
|
T | C | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-738T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536825 | ||||||
chr8:86536933
|
G | C | 1 | a0001c0001t0010g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-630G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86536933 | ||||||
chr8:86537183
|
A | C | 5 | a0001c0002t0006g0292a0001c0002t0006g0293a0001c0002t0009g0295others(2): Show | 5 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-380A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537183 | ||||||
chr8:86537215
|
A | G | 14 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(11): Show | 14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-348A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537215 | ||||||
chr8:86537226
|
C | T | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-337C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537226 | ||||||
chr8:86537369
|
A | G | 1 | a0001c0001t0009g0019 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460-194A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537369 | ||||||
chr8:86537400
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.460-163C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 6/16 | chr8 | 86537400 | ||||||
chr8:86537738
|
A | G | 1 | a0001c0001t0010g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+92A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537738 | ||||||
chr8:86537966
|
G | C | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+320G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537966 | ||||||
chr8:86537966
|
GTC | G | 36 | a0001c0001t0001g0285a0001c0001t0004g0160a0001c0002t0004g0300others(33): Show | 36 | HG01069.hp1 HG01081.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.543+341_543+342del others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537966 | |||||
chr8:86537966
|
GTCTC | G | 9 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0111others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+339_543+342del others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537966 | |||||
chr8:86537980
|
C | G | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.543+334C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537980 | ||||||
chr8:86537985
|
T | A | 4 | a0001c0002t0004g0300a0001c0002t0007g0317a0001c0002t0010g0302others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+339T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537985 | ||||||
chr8:86537985
|
T | TCA | 41 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(38): Show | 42 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.543+340_543+341ins others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537985 | |||||
chr8:86537987
|
T | A | 59 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(56): Show | 60 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.543+341T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86537987 | ||||||
chr8:86537987
|
T | TCA | 107 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0146others(104): Show | 109 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.543+361_543+362dup others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537987 | |||||
chr8:86537987
|
T | TCTCA | 11 | a0001c0001t0001g0248a0001c0001t0002g0251a0001c0001t0003g0243others(8): Show | 11 | HG00597.hp1 HG02056.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+342_543+343ins others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86537987 | |||||
chr8:86538699
|
C | T | 3 | a0001c0001t0001g0126a0001c0001t0003g0125a0001c0001t0003g0127 | 3 | HG02056.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.543+1053C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538699 | ||||||
chr8:86538769
|
A | G | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+1123A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538769 | ||||||
chr8:86538827
|
C | G | 1 | a0004c0013t0005g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543+1181C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538827 | ||||||
chr8:86538861
|
G | C | 14 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(11): Show | 14 | HG01099.hp2 HG02698.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+1215G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86538861 | ||||||
chr8:86539163
|
T | C | 32 | a0001c0001t0004g0160a0003c0004t0004g0156a0003c0004t0004g0157others(29): Show | 32 | HG01069.hp1 HG01081.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.544-1082T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539163 | ||||||
chr8:86539196
|
G | A | 4 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0233others(1): Show | 4 | HG00738.hp1 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-1049G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539196 | ||||||
chr8:86539227
|
C | A | 1 | a0001c0001t0017g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.544-1018C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539227 | ||||||
chr8:86539336
|
T | C | 2 | a0001c0001t0001g0063a0010c0016t0008g0079 | 2 | HG01109.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.544-909T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539336 | ||||||
chr8:86539358
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.544-887G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539358 | ||||||
chr8:86539467
|
A | G | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-778A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539467 | ||||||
chr8:86539547
|
T | A | 1 | a0001c0001t0004g0272 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.544-698T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539547 | ||||||
chr8:86539656
|
C | T | 40 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(37): Show | 41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.544-589C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539656 | ||||||
chr8:86539660
|
G | GT | 27 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0115others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.544-565dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86539660 | |||||
chr8:86539660
|
G | GTT | 121 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(118): Show | 123 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.544-566_544-565dup others(2): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86539660 | |||||
chr8:86539660
|
G | GTTT | 29 | a0001c0001t0001g0235a0001c0001t0001g0242a0001c0001t0002g0148others(26): Show | 29 | HG00438.hp1 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.544-567_544-565dup others(3): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr8 | 86539660 | |||||
chr8:86539688
|
T | C | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-557T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539688 | ||||||
chr8:86539890
|
C | G | 1 | a0001c0001t0004g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.544-355C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539890 | ||||||
chr8:86539912
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.544-333G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539912 | ||||||
chr8:86539916
|
C | T | 1 | a0002c0003t0005g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.544-329C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539916 | ||||||
chr8:86539956
|
C | T | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.544-289C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539956 | ||||||
chr8:86539958
|
C | A | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-287C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539958 | ||||||
chr8:86539984
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.544-261T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86539984 | ||||||
chr8:86540198
|
T | C | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.544-47T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86540198 | ||||||
chr8:86540205
|
G | A | 1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.544-40G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 7/16 | chr8 | 86540205 | ||||||
chr8:86540567
|
G | A | 5 | a0001c0002t0006g0292a0001c0002t0006g0293a0001c0002t0009g0295others(2): Show | 5 | HG02559.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+233G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540567 | ||||||
chr8:86540767
|
G | C | 4 | a0001c0001t0007g0134a0001c0001t0007g0137a0001c0001t0007g0138others(1): Show | 4 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+433G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540767 | ||||||
chr8:86540784
|
T | C | 1 | a0001c0001t0010g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.633+450T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540784 | ||||||
chr8:86540859
|
T | A | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.633+525T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540859 | ||||||
chr8:86540972
|
A | G | 1 | a0002c0003t0005g0182 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.633+638A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86540972 | ||||||
chr8:86541011
|
TG | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0077 | 3 | NA18966.hp1 NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.633+678delG | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541011 | ||||||
chr8:86541069
|
T | A | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.633+735T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541069 | ||||||
chr8:86541120
|
A | G | 334 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(331): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.633+786A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541120 | ||||||
chr8:86541425
|
C | T | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+1091C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541425 | ||||||
chr8:86541465
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.633+1131A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541465 | ||||||
chr8:86541506
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.633+1172C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541506 | ||||||
chr8:86541652
|
C | T | 2 | a0001c0008t0002g0297a0001c0008t0004g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.633+1318C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541652 | ||||||
chr8:86541705
|
T | TA | 35 | a0001c0001t0001g0010a0001c0001t0001g0061a0001c0001t0001g0075others(32): Show | 36 | HG00099.hp2 HG00609.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.633+1390dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr8 | 86541705 | |||||
chr8:86541721
|
A | C | 2 | a0001c0001t0003g0051a0002c0003t0004g0086 | 2 | HG00323.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.633+1387A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541721 | ||||||
chr8:86541945
|
G | C | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.633+1611G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86541945 | ||||||
chr8:86542203
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.633+1869C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542203 | ||||||
chr8:86542222
|
A | G | 1 | a0003c0004t0004g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.633+1888A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542222 | ||||||
chr8:86542328
|
A | G | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.633+1994A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542328 | ||||||
chr8:86542422
|
G | A | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.633+2088G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542422 | ||||||
chr8:86542496
|
G | T | 4 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+2162G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542496 | ||||||
chr8:86542683
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.634-2057G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542683 | ||||||
chr8:86542729
|
C | A | 1 | a0001c0001t0004g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.634-2011C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542729 | ||||||
chr8:86542741
|
C | T | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.634-1999C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542741 | ||||||
chr8:86542742
|
G | A | 40 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(37): Show | 41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.634-1998G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542742 | ||||||
chr8:86542815
|
A | G | 56 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(53): Show | 56 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.634-1925A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86542815 | ||||||
chr8:86543614
|
G | A | 1 | a0001c0001t0010g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.634-1126G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543614 | ||||||
chr8:86543633
|
G | A | 2 | a0001c0002t0001g0303a0001c0002t0002g0311 | 2 | HG02132.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.634-1107G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543633 | ||||||
chr8:86543706
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.634-1034G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543706 | ||||||
chr8:86543812
|
G | A | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.634-928G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543812 | ||||||
chr8:86543826
|
A | G | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.634-914A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543826 | ||||||
chr8:86543836
|
T | C | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.634-904T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86543836 | ||||||
chr8:86544120
|
G | A | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.634-620G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544120 | ||||||
chr8:86544154
|
T | G | 2 | a0001c0001t0001g0008a0001c0010t0001g0072 | 2 | NA18946.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.634-586T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544154 | ||||||
chr8:86544204
|
T | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-536T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544204 | ||||||
chr8:86544437
|
T | G | 1 | a0001c0001t0004g0032 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.634-303T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544437 | ||||||
chr8:86544463
|
G | A | 94 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0205others(91): Show | 96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.634-277G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544463 | ||||||
chr8:86544535
|
C | T | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.634-205C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544535 | ||||||
chr8:86544567
|
A | G | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-173A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544567 | ||||||
chr8:86544676
|
G | A | 1 | a0002c0003t0002g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.634-64G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544676 | ||||||
chr8:86544693
|
A | C | 1 | a0001c0001t0004g0032 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.634-47A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544693 | ||||||
chr8:86544726
|
A | G | 1 | a0001c0001t0003g0124 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.634-14A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 8/16 | chr8 | 86544726 | ||||||
chr8:86544925
|
C | T | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+87C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86544925 | ||||||
chr8:86544964
|
G | A | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.732+126G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86544964 | ||||||
chr8:86545123
|
T | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+285T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545123 | ||||||
chr8:86545129
|
T | G | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+291T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545129 | ||||||
chr8:86545154
|
T | G | 2 | a0001c0001t0008g0058a0002c0003t0005g0037 | 2 | NA18980.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.732+316T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545154 | ||||||
chr8:86545206
|
A | C | 4 | a0001c0002t0006g0292a0001c0002t0006g0293a0001c0002t0009g0295others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+368A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545206 | ||||||
chr8:86545313
|
C | G | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+475C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545313 | ||||||
chr8:86545561
|
C | T | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.732+723C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545561 | ||||||
chr8:86545636
|
G | A | 3 | a0001c0001t0004g0201a0001c0001t0004g0208a0001c0001t0004g0232 | 3 | NA18939.hp1 NA18960.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.732+798G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545636 | ||||||
chr8:86545714
|
C | G | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.732+876C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545714 | ||||||
chr8:86545742
|
G | T | 1 | a0001c0001t0002g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.733-853G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545742 | ||||||
chr8:86545910
|
A | G | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-685A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545910 | ||||||
chr8:86545914
|
T | G | 150 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(147): Show | 152 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.733-681T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545914 | ||||||
chr8:86545982
|
G | T | 56 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0275others(53): Show | 56 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.733-613G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86545982 | ||||||
chr8:86546055
|
C | A | 150 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(147): Show | 152 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.733-540C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546055 | ||||||
chr8:86546118
|
C | T | 15 | a0001c0001t0002g0141a0001c0001t0004g0132a0001c0001t0004g0135others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.733-477C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546118 | ||||||
chr8:86546176
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.733-419T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546176 | ||||||
chr8:86546197
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.733-398G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546197 | ||||||
chr8:86546427
|
T | C | 1 | a0001c0001t0010g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.733-168T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 9/16 | chr8 | 86546427 | ||||||
chr8:86546862
|
C | A | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+181C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86546862 | ||||||
chr8:86546926
|
G | C | 5 | a0003c0004t0007g0158a0003c0004t0007g0172a0003c0004t0007g0173others(2): Show | 5 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+245G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86546926 | ||||||
chr8:86547004
|
C | T | 2 | a0001c0008t0002g0297a0001c0008t0004g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.819+323C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547004 | ||||||
chr8:86547214
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820-497A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547214 | ||||||
chr8:86547513
|
A | G | 1 | a0002c0003t0005g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.820-198A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547513 | ||||||
chr8:86547553
|
TA | T | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.820-157delA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547553 | ||||||
chr8:86547573
|
A | G | 1 | a0001c0002t0002g0335 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.820-138A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | chr8 | 86547573 | ||||||
chr8:86547651
|
GT | G | 33 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0094others(30): Show | 33 | HG00597.hp2 HG00673.hp1 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.820-54delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr8 | 86547651 | |||||
chr8:86547923
|
T | C | 40 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(37): Show | 41 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.879+153T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86547923 | ||||||
chr8:86547952
|
C | T | 2 | a0001c0002t0005g0325a0001c0002t0005g0326 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.879+182C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86547952 | ||||||
chr8:86548080
|
A | G | 4 | a0001c0001t0007g0134a0001c0001t0007g0137a0001c0001t0007g0138others(1): Show | 4 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-221A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86548080 | ||||||
chr8:86548083
|
A | G | 57 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(54): Show | 58 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.880-218A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 11/16 | chr8 | 86548083 | ||||||
chr8:86548481
|
C | T | 2 | a0003c0004t0004g0162a0004c0006t0005g0161 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1013+47C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86548481 | ||||||
chr8:86548625
|
T | G | 60 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(57): Show | 61 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1013+191T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86548625 | ||||||
chr8:86548986
|
A | G | 1 | a0001c0017t0001g0105 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1013+552A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86548986 | ||||||
chr8:86549131
|
C | G | 1 | a0003c0004t0004g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1013+697C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549131 | ||||||
chr8:86549156
|
T | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013+722T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549156 | ||||||
chr8:86549171
|
G | A | 2 | a0001c0008t0002g0297a0001c0008t0004g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1013+737G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549171 | ||||||
chr8:86549172
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1013+738G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549172 | ||||||
chr8:86549223
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1013+789A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549223 | ||||||
chr8:86549514
|
T | A | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1013+1080T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549514 | ||||||
chr8:86549750
|
G | C | 37 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(34): Show | 38 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014-1296G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549750 | ||||||
chr8:86549879
|
C | G | 1 | a0001c0001t0002g0191 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1014-1167C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86549879 | ||||||
chr8:86550052
|
G | A | 210 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0183others(207): Show | 213 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.1014-994G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550052 | ||||||
chr8:86550102
|
T | C | 37 | a0001c0002t0001g0303a0001c0002t0001g0310a0001c0002t0001g0319others(34): Show | 38 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014-944T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550102 | ||||||
chr8:86550291
|
C | G | 4 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-755C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550291 | ||||||
chr8:86550492
|
C | T | 1 | a0004c0006t0005g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1014-554C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550492 | ||||||
chr8:86550494
|
G | C | 8 | a0001c0001t0001g0220a0001c0001t0002g0191a0001c0001t0003g0202others(5): Show | 8 | HG00544.hp2 HG02071.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014-552G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550494 | ||||||
chr8:86550540
|
A | C | 5 | a0001c0002t0002g0289a0002c0005t0004g0287a0002c0005t0004g0288others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-506A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550540 | ||||||
chr8:86550558
|
T | C | 213 | a0001c0001t0001g0107a0001c0001t0001g0146a0001c0001t0001g0181others(210): Show | 216 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.1014-488T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550558 | ||||||
chr8:86550575
|
G | A | 3 | a0005c0007t0010g0278a0005c0007t0010g0279a0005c0007t0010g0280 | 3 | HG03516.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1014-471G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550575 | ||||||
chr8:86550867
|
A | C | 3 | a0001c0001t0004g0160a0002c0003t0002g0144a0004c0006t0002g0163 | 3 | HG01069.hp1 HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1014-179A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550867 | ||||||
chr8:86550970
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014-76G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 12/16 | chr8 | 86550970 | ||||||
chr8:86551403
|
G | T | 1 | a0001c0001t0003g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1120+169G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551403 | ||||||
chr8:86551439
|
C | T | 18 | a0001c0001t0004g0160a0001c0001t0010g0177a0001c0001t0013g0130others(15): Show | 18 | HG01069.hp1 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1120+205C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551439 | ||||||
chr8:86551517
|
T | C | 4 | a0001c0001t0009g0019a0003c0004t0009g0186a0003c0004t0009g0187others(1): Show | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+283T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551517 | ||||||
chr8:86551650
|
G | A | 89 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0069others(86): Show | 91 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1120+416G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551650 | ||||||
chr8:86551691
|
T | C | 3 | a0001c0001t0004g0132a0001c0002t0004g0300a0002c0003t0005g0139 | 3 | HG02055.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1120+457T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551691 | ||||||
chr8:86551770
|
C | T | 2 | a0001c0001t0002g0005a0001c0002t0002g0289 | 2 | HG00741.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1120+536C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86551770 | ||||||
chr8:86552085
|
T | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(85): Show | 90 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1120+851T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552085 | ||||||
chr8:86552100
|
T | G | 1 | a0001c0010t0001g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1120+866T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552100 | ||||||
chr8:86552101
|
A | G | 1 | a0001c0010t0001g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1120+867A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552101 | ||||||
chr8:86552104
|
T | TGGGAGGG others(12): Show |
1 | a0001c0010t0001g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1120+871_1120+872i others(21): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552104 | |||||
chr8:86552269
|
C | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(200): Show | 204 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1120+1035C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552269 | ||||||
chr8:86552358
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1120+1124T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552358 | ||||||
chr8:86552407
|
T | C | 1 | a0001c0001t0004g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1120+1173T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552407 | ||||||
chr8:86552418
|
T | A | 1 | a0003c0004t0004g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1120+1184T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552418 | ||||||
chr8:86552463
|
TAATTAGC others(14): Show |
T | 1 | a0001c0001t0001g0189 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1120+1233_1120+125 others(25): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552463 | |||||
chr8:86552549
|
G | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1120+1315G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552549 | ||||||
chr8:86552564
|
G | C | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1120+1330G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552564 | ||||||
chr8:86552574
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1120+1340C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552574 | ||||||
chr8:86552576
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0181a0001c0002t0001g0321 | 3 | HG00099.hp2 NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1120+1342A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552576 | ||||||
chr8:86552837
|
A | AT | 72 | a0001c0001t0002g0004a0001c0001t0002g0028a0001c0001t0002g0041others(69): Show | 72 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1120+1621dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552837 | |||||
chr8:86552837
|
AT | A | 8 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0129others(5): Show | 8 | HG01975.hp1 HG02897.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+1621delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552837 | |||||
chr8:86552856
|
C | T | 2 | a0001c0001t0002g0005a0001c0002t0002g0289 | 2 | HG00741.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1120+1622C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552856 | ||||||
chr8:86552862
|
G | A | 65 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(62): Show | 65 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1120+1628G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552862 | ||||||
chr8:86552908
|
T | C | 257 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(254): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1120+1674T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552908 | ||||||
chr8:86552930
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1120+1696C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552930 | ||||||
chr8:86552932
|
C | T | 5 | a0001c0001t0006g0011a0001c0001t0006g0022a0001c0001t0006g0023others(2): Show | 5 | HG01167.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+1698C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552932 | ||||||
chr8:86552958
|
G | GCAGCCCC others(57): Show |
1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1120+1725_1120+172 others(68): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552958 | |||||
chr8:86552962
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1120+1728G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552962 | ||||||
chr8:86552962
|
G | GCACCCCC others(6): Show |
1 | a0001c0001t0001g0205 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1120+1729_1120+173 others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCC | 29 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0088others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1120+1742_1120+174 others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCACCC others(51): Show |
1 | a0009c0015t0001g0048 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1120+1731_1120+173 others(62): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCC | 27 | a0001c0001t0002g0042a0001c0001t0002g0057a0001c0001t0002g0085others(24): Show | 27 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1120+1741_1120+174 others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(4): Show |
1 | a0001c0002t0019g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1120+1736_1120+173 others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(6): Show |
4 | a0001c0001t0001g0222a0001c0002t0001g0319a0001c0002t0001g0322others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1736_1120+173 others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(3): Show |
4 | a0001c0001t0001g0106a0001c0001t0004g0035a0001c0001t0006g0067others(1): Show | 4 | HG02886.hp2 HG03490.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1735_1120+174 others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(4): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(1): Show | 4 | HG00735.hp1 NA19009.hp2 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+1734_1120+174 others(15): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(5): Show |
8 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0061others(5): Show | 8 | HG00558.hp2 HG01975.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+1733_1120+174 others(16): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(6): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0113a0001c0001t0001g0117others(3): Show | 6 | HG01255.hp1 HG01358.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+1732_1120+174 others(17): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(7): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0068others(4): Show | 7 | HG01106.hp1 HG01192.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+1731_1120+174 others(18): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(8): Show |
6 | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0104others(3): Show | 6 | HG02083.hp2 HG02129.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+1730_1120+174 others(19): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(9): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0094others(5): Show | 8 | HG01496.hp1 HG01496.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+1729_1120+174 others(20): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(10): Show |
9 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0108others(6): Show | 9 | HG00609.hp1 HG01928.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120+1744_1120+174 others(21): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(11): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0242 | 2 | HG01109.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1120+1744_1120+174 others(22): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(12): Show |
4 | a0001c0001t0001g0064a0001c0001t0001g0275a0001c0002t0001g0310others(1): Show | 4 | HG00735.hp2 HG01978.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1744_1120+174 others(23): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(13): Show |
1 | a0001c0010t0001g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1120+1744_1120+174 others(24): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552962
|
G | GCCCCCCC others(17): Show |
1 | a0001c0001t0006g0011 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1744_1120+174 others(28): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552962 | |||||
chr8:86552970
|
C | CCCG | 29 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0118others(26): Show | 29 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1120+1738_1120+173 others(7): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552970 | |||||
chr8:86552970
|
C | CCG | 30 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0107others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1120+1737_1120+173 others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552970 | |||||
chr8:86552970
|
C | G | 1 | a0001c0001t0003g0223 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1120+1736C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552970 | ||||||
chr8:86552972
|
C | CCCCCCA | 22 | a0002c0003t0004g0200a0002c0003t0005g0027a0002c0003t0005g0065others(19): Show | 22 | HG00733.hp1 HG01255.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1120+1743_1120+174 others(10): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552972 | |||||
chr8:86552972
|
C | CCCCCCCC others(3): Show |
1 | a0002c0003t0005g0182 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1120+1744_1120+174 others(14): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552972 | |||||
chr8:86552973
|
C | CT | 26 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0033others(23): Show | 28 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1120+1739_1120+174 others(5): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552973 | ||||||
chr8:86552973
|
C | T | 12 | a0001c0001t0004g0018a0001c0001t0004g0132a0001c0001t0007g0137others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1120+1739C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552973 | ||||||
chr8:86552979
|
G | A | 130 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(127): Show | 130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1120+1745G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552979 | ||||||
chr8:86552979
|
G | C | 9 | a0001c0001t0002g0141a0001c0001t0008g0090a0001c0002t0006g0267others(6): Show | 9 | HG02145.hp1 HG02647.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120+1745G>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86552979 | ||||||
chr8:86552980
|
C | CCCCCCCC others(8): Show |
1 | a0001c0001t0008g0090 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1120+1748_1120+174 others(19): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86552980 | |||||
chr8:86553098
|
T | C | 257 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(254): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1121-1753T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553098 | ||||||
chr8:86553277
|
A | T | 12 | a0001c0001t0004g0035a0001c0001t0004g0054a0001c0001t0004g0160others(9): Show | 12 | HG01069.hp1 HG01070.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-1574A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553277 | ||||||
chr8:86553366
|
C | G | 1 | a0001c0001t0003g0009 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1121-1485C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553366 | ||||||
chr8:86553483
|
A | T | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1121-1368A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553483 | ||||||
chr8:86553484
|
A | C | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1121-1367A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553484 | ||||||
chr8:86553509
|
A | G | 1 | a0003c0004t0004g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1121-1342A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553509 | ||||||
chr8:86553529
|
G | A | 17 | a0001c0001t0007g0134a0001c0001t0007g0137a0001c0001t0007g0138others(14): Show | 17 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1121-1322G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553529 | ||||||
chr8:86553703
|
C | T | 1 | a0002c0003t0005g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1121-1148C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553703 | ||||||
chr8:86553749
|
G | GT | 53 | a0001c0001t0001g0038a0001c0001t0001g0261a0001c0001t0002g0005others(50): Show | 54 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1121-1085dupT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86553749 | |||||
chr8:86553749
|
G | GTT | 67 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1121-1086_1121-108 others(6): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86553749 | |||||
chr8:86553749
|
GT | G | 20 | a0001c0001t0001g0091a0001c0001t0001g0285a0001c0001t0002g0253others(17): Show | 20 | HG01070.hp1 HG01884.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1121-1085delT | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr8 | 86553749 | |||||
chr8:86553828
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0118 | 2 | NA18956.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1121-1023T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553828 | ||||||
chr8:86553930
|
A | G | 142 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(139): Show | 143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1121-921A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553930 | ||||||
chr8:86553931
|
G | A | 257 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(254): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1121-920G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86553931 | ||||||
chr8:86554215
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1121-636A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554215 | ||||||
chr8:86554304
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1121-547C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554304 | ||||||
chr8:86554352
|
A | C | 2 | a0004c0006t0005g0159a0004c0006t0005g0174 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1121-499A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554352 | ||||||
chr8:86554537
|
A | G | 1 | a0001c0002t0006g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1121-314A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554537 | ||||||
chr8:86554595
|
G | T | 2 | a0003c0004t0004g0156a0003c0004t0004g0157 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1121-256G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554595 | ||||||
chr8:86554596
|
T | A | 2 | a0003c0004t0004g0156a0003c0004t0004g0157 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1121-255T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554596 | ||||||
chr8:86554645
|
G | A | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1121-206G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554645 | ||||||
chr8:86554687
|
T | C | 6 | a0001c0001t0006g0011a0001c0001t0006g0022a0001c0001t0006g0023others(3): Show | 6 | HG01167.hp2 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-164T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554687 | ||||||
chr8:86554803
|
G | A | 142 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(139): Show | 143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1121-48G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554803 | ||||||
chr8:86554848
|
T | C | 2 | a0001c0001t0004g0012a0001c0001t0004g0055 | 2 | NA18943.hp2 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.1121-3T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 14/16 | chr8 | 86554848 | ||||||
chr8:86555077
|
A | C | 142 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(139): Show | 143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1254+93A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555077 | ||||||
chr8:86555156
|
A | C | 9 | a0001c0001t0004g0018a0001c0001t0004g0132a0001c0002t0004g0300others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+172A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555156 | ||||||
chr8:86555199
|
T | C | 1 | a0003c0004t0004g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1254+215T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555199 | ||||||
chr8:86555234
|
C | CA | 25 | a0001c0001t0001g0053a0001c0001t0004g0018a0001c0001t0004g0132others(22): Show | 25 | HG01081.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1254+263dupA | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr8 | 86555234 | |||||
chr8:86555234
|
C | CAA | 15 | a0001c0001t0009g0019a0001c0001t0010g0177a0001c0002t0004g0336others(12): Show | 15 | HG01070.hp1 HG02572.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+262_1254+263d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr8 | 86555234 | |||||
chr8:86555300
|
G | T | 65 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(62): Show | 65 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1254+316G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555300 | ||||||
chr8:86555418
|
G | A | 41 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0012others(38): Show | 43 | HG01081.hp1 HG01243.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1254+434G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555418 | ||||||
chr8:86555478
|
A | G | 142 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(139): Show | 143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1254+494A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555478 | ||||||
chr8:86555549
|
A | T | 1 | a0001c0002t0009g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1255-553A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555549 | ||||||
chr8:86555620
|
A | C | 73 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(70): Show | 73 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1255-482A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555620 | ||||||
chr8:86555686
|
C | A | 8 | a0001c0001t0002g0028a0001c0001t0002g0042a0001c0001t0002g0102others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-416C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555686 | ||||||
chr8:86555709
|
TATTCTA | T | 13 | a0002c0003t0005g0027a0002c0003t0005g0142a0002c0003t0005g0143others(10): Show | 13 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-384_1255-379d others(8): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr8 | 86555709 | |||||
chr8:86555746
|
T | C | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1255-356T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555746 | ||||||
chr8:86555770
|
C | T | 9 | a0001c0001t0007g0134a0001c0001t0007g0137a0001c0001t0007g0138others(6): Show | 9 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255-332C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555770 | ||||||
chr8:86555906
|
G | A | 115 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0045others(112): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1255-196G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 15/16 | chr8 | 86555906 | ||||||
chr8:86556365
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1491+27C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86556365 | ||||||
chr8:86556416
|
T | G | 142 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(139): Show | 143 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1491+78T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86556416 | ||||||
chr8:86556943
|
T | C | 1 | a0002c0003t0005g0100 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1491+605T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86556943 | ||||||
chr8:86557120
|
G | A | 3 | a0001c0001t0002g0005a0001c0001t0002g0078a0001c0002t0002g0289 | 3 | HG00741.hp1 HG03579.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1491+782G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557120 | ||||||
chr8:86557196
|
C | T | 53 | a0001c0002t0005g0325a0001c0002t0005g0326a0002c0003t0002g0144others(50): Show | 54 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1491+858C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557196 | ||||||
chr8:86557217
|
T | G | 141 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(138): Show | 142 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.1491+879T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557217 | ||||||
chr8:86557249
|
T | C | 1 | a0001c0002t0014g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1491+911T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557249 | ||||||
chr8:86557261
|
A | G | 248 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(245): Show | 251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1491+923A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557261 | ||||||
chr8:86557297
|
C | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0190 | 3 | HG00438.hp2 HG02132.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1491+959C>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557297 | ||||||
chr8:86557337
|
C | T | 248 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(245): Show | 251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1492-951C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557337 | ||||||
chr8:86557414
|
C | G | 248 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(245): Show | 251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1492-874C>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557414 | ||||||
chr8:86557415
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1492-873C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557415 | ||||||
chr8:86557425
|
C | T | 58 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0012others(55): Show | 60 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1492-863C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557425 | ||||||
chr8:86557426
|
G | T | 1 | a0001c0001t0002g0265 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1492-862G>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557426 | ||||||
chr8:86557482
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(63): Show | 66 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1492-806A>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557482 | ||||||
chr8:86557516
|
T | C | 9 | a0001c0001t0004g0018a0001c0001t0004g0132a0001c0002t0004g0300others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1492-772T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557516 | ||||||
chr8:86557624
|
T | C | 2 | a0001c0001t0008g0089a0001c0001t0008g0090 | 2 | NA19010.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1492-664T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557624 | ||||||
chr8:86557755
|
T | TAC | 3 | a0001c0001t0004g0035a0001c0001t0004g0054a0001c0001t0004g0160 | 3 | HG01069.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1492-515_1492-514d others(4): Show |
CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr8 | 86557755 | |||||
chr8:86557884
|
T | G | 18 | a0001c0001t0007g0134a0001c0001t0007g0137a0001c0001t0007g0138others(15): Show | 18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1492-404T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557884 | ||||||
chr8:86557898
|
T | G | 18 | a0001c0001t0007g0134a0001c0001t0007g0137a0001c0001t0007g0138others(15): Show | 18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1492-390T>G | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557898 | ||||||
chr8:86557909
|
T | C | 248 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0028others(245): Show | 251 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1492-379T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557909 | ||||||
chr8:86557976
|
A | C | 57 | a0001c0001t0003g0009a0001c0001t0003g0029a0001c0001t0003g0030others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1492-312A>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86557976 | ||||||
chr8:86558019
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1492-269T>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558019 | ||||||
chr8:86558028
|
A | T | 1 | a0001c0001t0004g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492-260A>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558028 | ||||||
chr8:86558150
|
C | T | 5 | a0001c0002t0006g0267a0001c0002t0006g0268a0001c0002t0006g0269others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1492-138C>T | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558150 | ||||||
chr8:86558166
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG01192.hp1 HG01255.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492-122G>A | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558166 | ||||||
chr8:86558213
|
T | C | 1 | a0001c0002t0004g0336 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1492-75T>C | CPNE3 | ENSG00000085719.13 | transcript | ENST00000517490.6 | protein_coding | 16/16 | chr8 | 86558213 |