geneid | 51032 |
---|---|
ensemblid | ENSG00000215704.10 |
hgncid | 29995 |
symbol | CELA2B |
name | chymotrypsin like elastase 2B |
refseq_nuc | NM_015849.3 |
refseq_prot | NP_056933.3 |
ensembl_nuc | ENST00000375910.8 |
ensembl_prot | ENSP00000365075.3 |
mane_status | MANE Select |
chr | chr1 |
start | 15476104 |
end | 15491395 |
strand | + |
ver | v1.2 |
region | chr1:15476104-15491395 |
region5000 | chr1:15471104-15496395 |
regionname0 | CELA2B_chr1_15476104_15491395 |
regionname5000 | CELA2B_chr1_15471104_15496395 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 269 | 245 | 55 | 52 | 89 | 11 | 37 | 74 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0002 | 0/0 | 269 | 152 | 32 | 26 | 86 | 3 | 5 | 66 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0003 | 1/0 | 269 | 6 | 5 | 0 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0004 | 0/0 | 269 | 6 | 0 | 3 | 3 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0005 | 0/0 | 269 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0006 | 0/0 | 269 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0007 | 0/0 | 269 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 810 | 225 | 45 | 51 | 80 | 11 | 37 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0002 | 0/0 | 810 | 151 | 32 | 26 | 85 | 3 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0003 | 0/0 | 810 | 7 | 6 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0004 | 0/0 | 810 | 6 | 0 | 3 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0005 | 1/0 | 810 | 6 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0006 | 0/0 | 810 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0007 | 0/0 | 810 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0008 | 0/0 | 810 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0009 | 0/0 | 810 | 2 | 0 | 1 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0010 | 0/0 | 810 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0011 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0012 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0013 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
c0014 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 106 | 405 | 87 | 82 | 177 | 16 | 41 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
t0002 | 0/0 | 106 | 6 | 3 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
t0003 | 0/0 | 106 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
t0004 | 0/0 | 106 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 35 | 8 | 11 | 13 | 0 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0002 | 0/0 | 27 | 0 | 8 | 14 | 2 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0003 | 0/1 | 25 | 0 | 3 | 13 | 3 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0004 | 0/0 | 22 | 5 | 2 | 14 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0005 | 0/0 | 14 | 2 | 6 | 0 | 1 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0006 | 0/0 | 7 | 0 | 0 | 3 | 0 | 4 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0009 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0011 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0013 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0017 | 0/0 | 5 | 2 | 1 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0022 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0029 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0056 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0057 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 810 | 225 | 45 | 51 | 80 | 11 | 37 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0003 | 0/0 | 810 | 7 | 6 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0006 | 0/0 | 810 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0007 | 0/0 | 810 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0008 | 0/0 | 810 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0011 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0014 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0002c0002 | 0/0 | 810 | 151 | 32 | 26 | 85 | 3 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0002c0013 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0003c0005 | 1/0 | 810 | 6 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0004c0004 | 0/0 | 810 | 6 | 0 | 3 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0005c0010 | 0/0 | 810 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0006c0009 | 0/0 | 810 | 2 | 0 | 1 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0007c0012 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 915 | 216 | 40 | 51 | 77 | 11 | 36 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0001t0002 | 0/0 | 915 | 6 | 3 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0001t0003 | 0/0 | 915 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0001t0004 | 0/0 | 915 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0003t0001 | 0/0 | 915 | 7 | 6 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0006t0001 | 0/0 | 915 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0007t0001 | 0/0 | 915 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0008t0001 | 0/0 | 915 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0011t0001 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0001c0014t0001 | 0/0 | 915 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0002c0002t0001 | 0/0 | 915 | 151 | 32 | 26 | 85 | 3 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0002c0013t0001 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0003c0005t0001 | 1/0 | 915 | 6 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0004c0004t0001 | 0/0 | 915 | 6 | 0 | 3 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0005c0010t0001 | 0/0 | 915 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0006c0009t0001 | 0/0 | 915 | 2 | 0 | 1 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
a0007c0012t0001 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | copy fasta | chr1 | 15471104 | 15496395 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 24 | 0 | 8 | 11 | 2 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0003 | 0/1 | 21 | 0 | 3 | 10 | 3 | 4 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0005 | 0/0 | 14 | 2 | 6 | 0 | 1 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0013 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0022 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0029 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0056 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0057 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0002g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0003g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0003t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0006t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0007t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0007t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0007t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0008t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0011t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0001c0014t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0001 | 0/0 | 35 | 8 | 11 | 13 | 0 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0004 | 0/0 | 22 | 5 | 2 | 14 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0002c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0003c0005t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0003c0005t0001g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0004c0004t0001g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0004c0004t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0005c0010t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0006c0009t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0006c0009t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
a0007c0012t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0043 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00544 | hp2 | a0001 | c0011 | t0001 | g0003 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00642 | hp2 | a0001 | c0007 | t0001 | g0164 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01496 | hp2 | a0004 | c0004 | t0001 | g0009 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01516 | hp2 | a0005 | c0010 | t0001 | g0017 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01517 | hp2 | a0005 | c0010 | t0001 | g0017 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01934 | hp2 | a0004 | c0004 | t0001 | g0102 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01952 | hp1 | a0006 | c0009 | t0001 | g0009 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01978 | hp1 | a0004 | c0004 | t0001 | g0009 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02071 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02615 | hp1 | a0001 | c0007 | t0001 | g0053 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02723 | hp1 | a0001 | c0007 | t0001 | g0143 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0015 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02897 | hp1 | a0003 | c0005 | t0001 | g0015 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03130 | hp1 | a0001 | c0014 | t0001 | g0183 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03195 | hp2 | a0001 | c0007 | t0001 | g0053 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03225 | hp1 | a0003 | c0005 | t0001 | g0015 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18941 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18944 | hp1 | a0007 | c0012 | t0001 | g0040 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18953 | hp1 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18957 | hp1 | a0002 | c0013 | t0001 | g0101 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18964 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18966 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18972 | hp1 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18994 | hp1 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19005 | hp1 | a0006 | c0009 | t0001 | g0103 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19074 | hp1 | a0001 | c0008 | t0001 | g0034 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19088 | hp1 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20129 | hp1 | a0003 | c0005 | t0001 | g0015 | AFR | ASW | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ASW | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA21309 | hp1 | a0003 | c0005 | t0001 | g0015 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
homoSapiens_grch38 | hp1 | a0003 | c0005 | t0001 | g0074 | REF | REF | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15481125
|
C | A | 1 | a0007 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.157C>A | p.Gln53Lys | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/8 | 179/915 | 157/810 | 53/269 | chr1 | 15481125 | ||
chr1:15482272
|
G | A | 4 | a0002a0004a0006others(1): Show | 161 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
missense_variant | MODERATE | c.235G>A | p.Gly79Arg | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/8 | 257/915 | 235/810 | 79/269 | chr1 | 15482272 | ||
chr1:15482377
|
G | A | 2 | a0002a0007 | 153 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
missense_variant | MODERATE | c.340G>A | p.Asp114Asn | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/8 | 362/915 | 340/810 | 114/269 | chr1 | 15482377 | ||
chr1:15485937
|
A | G | 6 | a0001a0002a0004others(3): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
missense_variant | MODERATE | c.530A>G | p.Gln177Arg | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/8 | 552/915 | 530/810 | 177/269 | chr1 | 15485937 | ||
chr1:15487348
|
G | A | 1 | a0004 | 6 | HG01496.hp2 HG01934.hp2 HG01978.hp1 others(3): Show |
missense_variant | MODERATE | c.703G>A | p.Gly235Ser | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/8 | 725/915 | 703/810 | 235/269 | chr1 | 15487348 | ||
chr1:15487349
|
G | T | 1 | a0005 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.704G>T | p.Gly235Val | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/8 | 726/915 | 704/810 | 235/269 | chr1 | 15487349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15476131
|
T | A | 1 | a0001c0006 | 4 | NA18941.hp2 NA18953.hp1 NA18966.hp2 others(1): Show |
synonymous_variant | LOW | c.6T>A | p.Ile2Ile | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/8 | 28/915 | 6/810 | 2/269 | chr1 | 15476131 | ||
chr1:15476137
|
C | G | 1 | a0001c0006 | 4 | NA18941.hp2 NA18953.hp1 NA18966.hp2 others(1): Show |
synonymous_variant | LOW | c.12C>G | p.Thr4Thr | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/8 | 34/915 | 12/810 | 4/269 | chr1 | 15476137 | ||
chr1:15476521
|
G | A | 1 | a0001c0011 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.105G>A | p.Ala35Ala | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/8 | 127/915 | 105/810 | 35/269 | chr1 | 15476521 | ||
chr1:15483381
|
G | A | 7 | a0001c0003a0001c0014a0002c0002others(4): Show | 169 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(166): Show |
synonymous_variant | LOW | c.474G>A | p.Thr158Thr | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/8 | 496/915 | 474/810 | 158/269 | chr1 | 15483381 | ||
chr1:15485905
|
C | T | 1 | a0001c0008 | 3 | NA18994.hp1 NA19074.hp1 NA19088.hp1 |
synonymous_variant | LOW | c.498C>T | p.Asn166Asn | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/8 | 520/915 | 498/810 | 166/269 | chr1 | 15485905 | ||
chr1:15487341
|
T | C | 3 | a0001c0007a0001c0014a0002c0013 | 6 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.696T>C | p.His232His | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/8 | 718/915 | 696/810 | 232/269 | chr1 | 15487341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15476116
|
C | T | 1 | a0001c0001t0003 | 2 | HG02486.hp2 HG02965.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/8 | chr1 | 15476116 | ||||||
chr1:15491350
|
G | A | 1 | a0001c0001t0004 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 8/8 | 38 | chr1 | 15491350 | |||||
chr1:15491368
|
A | G | 1 | a0001c0001t0002 | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 8/8 | 56 | chr1 | 15491368 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15476293
|
C | T | 1 | a0001c0014t0001g0183 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.40+128C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/7 | chr1 | 15476293 | ||||||
chr1:15476430
|
G | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 18 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-27G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/7 | chr1 | 15476430 | ||||||
chr1:15476599
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.129+54C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476599 | ||||||
chr1:15476622
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129+77C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476622 | ||||||
chr1:15476843
|
A | G | 130 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(127): Show | 271 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.129+298A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476843 | ||||||
chr1:15476874
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0094others(1): Show | 6 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+329C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476874 | ||||||
chr1:15476892
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.129+347G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476892 | ||||||
chr1:15476965
|
AAG | A | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+426_129+427del others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15476965 | |||||
chr1:15476990
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0057a0001c0001t0001g0176others(7): Show | 14 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+445G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476990 | ||||||
chr1:15477063
|
A | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0057others(18): Show | 28 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.129+518A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477063 | ||||||
chr1:15477135
|
T | G | 1 | a0002c0002t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129+590T>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477135 | ||||||
chr1:15477178
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0057others(15): Show | 24 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.129+633C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477178 | ||||||
chr1:15477292
|
T | A | 1 | a0002c0002t0001g0100 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.129+747T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477292 | ||||||
chr1:15477356
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 10 | HG01884.hp1 HG02257.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+811C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477356 | ||||||
chr1:15477524
|
T | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 20 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+979T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477524 | ||||||
chr1:15477913
|
G | A | 1 | a0002c0013t0001g0101 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.129+1368G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477913 | ||||||
chr1:15478165
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0170 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.129+1620G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478165 | ||||||
chr1:15478201
|
C | CATATATA others(3): Show |
2 | a0001c0001t0001g0171a0001c0001t0002g0096 | 2 | HG02486.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.129+1663_129+1672d others(12): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | |||||
chr1:15478201
|
C | CATATATA others(5): Show |
2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1661_129+1672d others(14): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | |||||
chr1:15478201
|
C | CATATATA others(7): Show |
1 | a0001c0003t0001g0054 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.129+1659_129+1672d others(16): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | |||||
chr1:15478201
|
C | CATATATA others(9): Show |
1 | a0001c0003t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.129+1657_129+1672d others(18): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | |||||
chr1:15478209
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0002g0055a0001c0001t0002g0170 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.129+1672_129+1683d others(14): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478209 | |||||
chr1:15478213
|
TATATTGG others(1): Show |
T | 5 | a0001c0003t0001g0039a0004c0004t0001g0009a0004c0004t0001g0102others(2): Show | 10 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+1673_129+1680d others(10): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478213 | |||||
chr1:15478215
|
TATTGGG | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 213 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.129+1673_129+1678d others(8): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478215 | |||||
chr1:15478217
|
T | TATATATA others(18): Show |
1 | a0001c0014t0001g0183 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+1672_129+1673i others(27): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478217 | ||||||
chr1:15478217
|
TTGGG | T | 8 | a0001c0001t0001g0162a0001c0007t0001g0053a0002c0002t0001g0007others(5): Show | 17 | HG01891.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+1673_129+1676d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478217 | ||||||
chr1:15478218
|
T | A | 6 | a0001c0001t0001g0171a0001c0001t0002g0096a0001c0001t0002g0097others(3): Show | 7 | HG02451.hp2 HG02486.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1673T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478218 | ||||||
chr1:15478219
|
G | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0096a0001c0001t0002g0097others(3): Show | 7 | HG02451.hp2 HG02486.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1674G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478219 | ||||||
chr1:15478220
|
G | A | 8 | a0001c0001t0001g0171a0001c0001t0002g0096a0001c0001t0002g0097others(5): Show | 9 | HG00642.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+1675G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478220 | ||||||
chr1:15478221
|
G | T | 8 | a0001c0001t0001g0171a0001c0001t0002g0096a0001c0001t0002g0097others(5): Show | 9 | HG00642.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+1676G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478221 | ||||||
chr1:15478229
|
G | T | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1684G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478229 | ||||||
chr1:15478230
|
T | A | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1685T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478230 | ||||||
chr1:15478232
|
T | A | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1687T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478232 | ||||||
chr1:15478299
|
A | G | 2 | a0002c0002t0001g0157a0002c0002t0001g0158 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129+1754A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478299 | ||||||
chr1:15478369
|
T | G | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1824T>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478369 | ||||||
chr1:15478471
|
G | A | 1 | a0002c0002t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.129+1926G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478471 | ||||||
chr1:15478490
|
G | T | 4 | a0001c0001t0001g0171a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG02486.hp1 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1945G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478490 | ||||||
chr1:15478511
|
G | A | 1 | a0001c0003t0001g0039 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.129+1966G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478511 | ||||||
chr1:15478565
|
A | AT | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 8 | HG01169.hp2 HG02451.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.129+2037dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | |||||
chr1:15478565
|
AT | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(37): Show | 83 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.129+2037delT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | |||||
chr1:15478565
|
ATT | A | 80 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0056others(77): Show | 174 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.129+2036_129+2037d others(4): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | |||||
chr1:15478565
|
ATTT | A | 5 | a0001c0001t0001g0175a0001c0001t0002g0055a0001c0001t0002g0170others(2): Show | 6 | HG01109.hp2 HG02698.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+2035_129+2037d others(5): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | |||||
chr1:15478633
|
T | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0170 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.129+2088T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478633 | ||||||
chr1:15478789
|
AC | A | 3 | a0001c0003t0001g0054a0001c0003t0001g0169a0001c0014t0001g0183 | 4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+2245delC | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478789 | ||||||
chr1:15478911
|
C | A | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-2187C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478911 | ||||||
chr1:15478993
|
CG | C | 9 | a0002c0002t0001g0019a0002c0002t0001g0040a0002c0002t0001g0107others(6): Show | 12 | HG00673.hp1 NA18939.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.130-2098delG | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478993 | |||||
chr1:15479052
|
G | A | 3 | a0001c0007t0001g0053a0001c0007t0001g0143a0001c0007t0001g0164 | 4 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2046G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479052 | ||||||
chr1:15479080
|
G | A | 1 | a0001c0001t0001g0050 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.130-2018G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479080 | ||||||
chr1:15479129
|
G | C | 4 | a0001c0001t0001g0171a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG02486.hp1 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1969G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479129 | ||||||
chr1:15479167
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(29): Show | 75 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.130-1931C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479167 | ||||||
chr1:15479227
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(29): Show | 75 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.130-1871G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479227 | ||||||
chr1:15479397
|
T | C | 9 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(6): Show | 11 | HG02451.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-1701T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479397 | ||||||
chr1:15479607
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.130-1491C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479607 | ||||||
chr1:15479634
|
A | G | 2 | a0002c0002t0001g0026a0002c0002t0001g0141 | 4 | HG01099.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1464A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479634 | ||||||
chr1:15479726
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130-1372T>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479726 | ||||||
chr1:15479749
|
T | C | 5 | a0002c0002t0001g0041a0002c0002t0001g0104a0002c0002t0001g0112others(2): Show | 6 | HG00597.hp1 NA18966.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-1349T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479749 | ||||||
chr1:15480252
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130-846C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480252 | ||||||
chr1:15480277
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.130-821G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480277 | ||||||
chr1:15480337
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 8 | NA18951.hp1 NA18954.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-761G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480337 | ||||||
chr1:15480504
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.130-594G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480504 | ||||||
chr1:15480507
|
G | A | 1 | a0001c0003t0001g0039 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.130-591G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480507 | ||||||
chr1:15480556
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-542C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480556 | ||||||
chr1:15480645
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130-453A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480645 | ||||||
chr1:15480647
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(30): Show | 76 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.130-451T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480647 | ||||||
chr1:15480798
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.130-300G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480798 | ||||||
chr1:15480885
|
C | A | 1 | a0001c0003t0001g0039 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.130-213C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480885 | ||||||
chr1:15480898
|
A | AT | 35 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0016others(32): Show | 71 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.130-186dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15480898 | |||||
chr1:15481026
|
G | A | 5 | a0002c0002t0001g0024a0002c0002t0001g0030a0002c0002t0001g0115others(2): Show | 9 | HG00673.hp2 HG02040.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.130-72G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15481026 | ||||||
chr1:15481235
|
C | T | 1 | a0001c0001t0001g0028 | 3 | HG00323.hp2 HG01069.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.227+40C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481235 | ||||||
chr1:15481285
|
G | A | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+90G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481285 | ||||||
chr1:15481318
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0173 | 3 | HG02723.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.227+123G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481318 | ||||||
chr1:15481366
|
T | C | 1 | a0001c0001t0003g0052 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.227+171T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481366 | ||||||
chr1:15481488
|
A | G | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+293A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481488 | ||||||
chr1:15481703
|
C | T | 68 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(65): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.227+508C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481703 | ||||||
chr1:15481709
|
C | G | 1 | a0002c0002t0001g0137 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.227+514C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481709 | ||||||
chr1:15481747
|
C | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-518C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481747 | ||||||
chr1:15481794
|
C | T | 83 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(80): Show | 171 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.228-471C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481794 | ||||||
chr1:15481881
|
G | A | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-384G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481881 | ||||||
chr1:15482011
|
TAG | T | 75 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(72): Show | 161 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.228-251_228-250del others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 15482011 | |||||
chr1:15482014
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.228-251A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482014 | ||||||
chr1:15482159
|
G | C | 1 | a0002c0002t0001g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.228-106G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482159 | ||||||
chr1:15482163
|
A | T | 1 | a0002c0002t0001g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.228-102A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482163 | ||||||
chr1:15482207
|
C | T | 71 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(68): Show | 153 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.228-58C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482207 | ||||||
chr1:15482250
|
A | C | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-15A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482250 | ||||||
chr1:15482428
|
T | C | 1 | a0002c0002t0001g0119 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.356+35T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482428 | ||||||
chr1:15482502
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.356+109G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482502 | ||||||
chr1:15482541
|
G | A | 77 | a0001c0003t0001g0039a0001c0003t0001g0087a0002c0002t0001g0001others(74): Show | 164 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.356+148G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482541 | ||||||
chr1:15482646
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.356+253G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482646 | ||||||
chr1:15482705
|
C | T | 1 | a0002c0002t0001g0111 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.356+312C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482705 | ||||||
chr1:15482826
|
C | G | 1 | a0002c0002t0001g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.356+433C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482826 | ||||||
chr1:15482867
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.357-397G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482867 | ||||||
chr1:15482871
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.357-393C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482871 | ||||||
chr1:15482933
|
C | T | 76 | a0001c0003t0001g0085a0002c0002t0001g0001a0002c0002t0001g0004others(73): Show | 162 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.357-331C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482933 | ||||||
chr1:15482941
|
A | AC | 120 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(117): Show | 252 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.357-322dupC | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 15482941 | |||||
chr1:15483051
|
TGCTGGCA others(6): Show |
T | 3 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0177 | 4 | HG01167.hp1 HG01175.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-184_357-172del others(13): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 15483051 | |||||
chr1:15483097
|
G | A | 2 | a0002c0002t0001g0043a0002c0002t0001g0121 | 3 | HG00140.hp1 HG00741.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.357-167G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483097 | ||||||
chr1:15483106
|
C | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(30): Show | 76 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.357-158C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483106 | ||||||
chr1:15483211
|
T | C | 120 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(117): Show | 252 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.357-53T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483211 | ||||||
chr1:15483246
|
G | A | 4 | a0002c0002t0001g0007a0002c0002t0001g0099a0002c0002t0001g0159others(1): Show | 10 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-18G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483246 | ||||||
chr1:15483470
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.493+70C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483470 | ||||||
chr1:15483511
|
G | C | 1 | a0001c0003t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+111G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483511 | ||||||
chr1:15483656
|
G | A | 1 | a0001c0014t0001g0183 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.493+256G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483656 | ||||||
chr1:15483677
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(31): Show | 78 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.493+277C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483677 | ||||||
chr1:15483695
|
A | G | 1 | a0002c0002t0001g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.493+295A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483695 | ||||||
chr1:15483704
|
G | C | 1 | a0002c0002t0001g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.493+304G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483704 | ||||||
chr1:15483713
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.493+313A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483713 | ||||||
chr1:15483757
|
G | A | 76 | a0001c0003t0001g0085a0002c0002t0001g0001a0002c0002t0001g0004others(73): Show | 162 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.493+357G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483757 | ||||||
chr1:15483782
|
C | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.493+382C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483782 | ||||||
chr1:15483801
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.493+401C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483801 | ||||||
chr1:15483803
|
C | G | 3 | a0001c0003t0001g0054a0001c0003t0001g0169a0001c0014t0001g0183 | 4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+403C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483803 | ||||||
chr1:15483827
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.493+427C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483827 | ||||||
chr1:15483851
|
T | C | 132 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(129): Show | 269 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.493+451T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483851 | ||||||
chr1:15483929
|
CA | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(37): Show | 84 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.493+541delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15483929 | |||||
chr1:15484021
|
G | A | 1 | a0002c0002t0001g0044 | 2 | NA18974.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.493+621G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484021 | ||||||
chr1:15484120
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0147others(5): Show | 17 | HG01975.hp2 HG01981.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.493+720A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484120 | ||||||
chr1:15484129
|
T | C | 114 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(111): Show | 245 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.493+729T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484129 | ||||||
chr1:15484158
|
A | G | 2 | a0001c0003t0001g0054a0001c0003t0001g0169 | 3 | HG02451.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.493+758A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484158 | ||||||
chr1:15484193
|
C | T | 70 | a0001c0003t0001g0085a0002c0002t0001g0001a0002c0002t0001g0004others(67): Show | 150 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.493+793C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484193 | ||||||
chr1:15484243
|
C | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.493+843C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484243 | ||||||
chr1:15484301
|
A | C | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.493+901A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484301 | ||||||
chr1:15484343
|
A | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.493+943A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484343 | ||||||
chr1:15484498
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493+1098G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484498 | ||||||
chr1:15484570
|
G | A | 2 | a0002c0002t0001g0026a0002c0002t0001g0141 | 4 | HG01099.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+1170G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484570 | ||||||
chr1:15484641
|
C | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(121): Show | 260 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.493+1241C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484641 | ||||||
chr1:15484701
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.494-1200T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484701 | ||||||
chr1:15484728
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0001g0083others(1): Show | 8 | NA18942.hp1 NA18948.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.494-1173C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484728 | ||||||
chr1:15484772
|
CA | C | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-1128delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484772 | ||||||
chr1:15484828
|
G | T | 1 | a0001c0003t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-1073G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484828 | ||||||
chr1:15484848
|
T | C | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-1053T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484848 | ||||||
chr1:15484851
|
C | T | 87 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(84): Show | 176 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.494-1050C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484851 | ||||||
chr1:15484901
|
A | ATT | 7 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(4): Show | 9 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.494-987_494-986dup others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15484901 | |||||
chr1:15484901
|
AT | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0147a0002c0002t0001g0115others(3): Show | 9 | HG00741.hp1 HG01106.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-986delT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15484901 | |||||
chr1:15484937
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0091 | 3 | HG01168.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.494-964G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484937 | ||||||
chr1:15484986
|
C | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-915C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484986 | ||||||
chr1:15485085
|
G | A | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-816G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485085 | ||||||
chr1:15485197
|
C | T | 77 | a0001c0001t0001g0082a0001c0003t0001g0085a0002c0002t0001g0001others(74): Show | 163 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.494-704C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485197 | ||||||
chr1:15485325
|
C | T | 1 | a0002c0002t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.494-576C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485325 | ||||||
chr1:15485366
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.494-535G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485366 | ||||||
chr1:15485383
|
A | AGATAAGT others(1): Show |
82 | a0001c0001t0001g0082a0001c0003t0001g0039a0001c0003t0001g0054others(79): Show | 170 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.494-517_494-510dup others(8): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15485383 | |||||
chr1:15485417
|
CA | C | 81 | a0001c0003t0001g0039a0001c0003t0001g0054a0001c0003t0001g0085others(78): Show | 169 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.494-477delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15485417 | |||||
chr1:15485499
|
A | G | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-402A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485499 | ||||||
chr1:15485641
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.494-260G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485641 | ||||||
chr1:15485801
|
G | A | 4 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(1): Show | 5 | HG02132.hp2 NA18967.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-100G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485801 | ||||||
chr1:15486170
|
G | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0016others(22): Show | 61 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.639+124G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486170 | ||||||
chr1:15486383
|
G | T | 1 | a0001c0014t0001g0183 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.639+337G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486383 | ||||||
chr1:15486453
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0070 | 6 | HG00099.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+407T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486453 | ||||||
chr1:15486472
|
C | CA | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0083others(3): Show | 6 | HG02976.hp1 NA18950.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+435dupA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 15486472 | |||||
chr1:15486593
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.639+547G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486593 | ||||||
chr1:15486898
|
A | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0100 | 4 | NA18952.hp1 NA18975.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-387A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486898 | ||||||
chr1:15487108
|
G | A | 1 | a0002c0002t0001g0108 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.640-177G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487108 | ||||||
chr1:15487115
|
A | T | 6 | a0001c0001t0001g0171a0001c0001t0002g0055a0001c0001t0002g0096others(3): Show | 7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.640-170A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487115 | ||||||
chr1:15487239
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.640-46G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487239 | ||||||
chr1:15487256
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.640-29C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487256 | ||||||
chr1:15487258
|
A | C | 4 | a0004c0004t0001g0009a0004c0004t0001g0102a0006c0009t0001g0009others(1): Show | 8 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-27A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487258 | ||||||
chr1:15487261
|
C | G | 4 | a0004c0004t0001g0009a0004c0004t0001g0102a0006c0009t0001g0009others(1): Show | 8 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-24C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487261 | ||||||
chr1:15487474
|
A | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(141): Show | 289 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.792+37A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487474 | ||||||
chr1:15487491
|
C | T | 3 | a0001c0007t0001g0053a0001c0007t0001g0143a0001c0007t0001g0164 | 4 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+54C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487491 | ||||||
chr1:15487676
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0147 | 6 | NA18954.hp1 NA18969.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+239G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487676 | ||||||
chr1:15487691
|
C | T | 131 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(128): Show | 270 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.792+254C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487691 | ||||||
chr1:15487883
|
C | A | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.792+446C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487883 | ||||||
chr1:15487980
|
C | CCT | 142 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(139): Show | 286 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.792+543_792+544ins others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487980 | ||||||
chr1:15488078
|
C | T | 5 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+641C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488078 | ||||||
chr1:15488165
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.792+728T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488165 | ||||||
chr1:15488172
|
A | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG01069.hp2 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.792+735A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488172 | ||||||
chr1:15488228
|
A | AT | 12 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0057others(9): Show | 18 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.792+802dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15488228 | |||||
chr1:15488466
|
GA | G | 5 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1031delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15488466 | |||||
chr1:15488542
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0071 | 8 | HG02074.hp2 NA18952.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.792+1105G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488542 | ||||||
chr1:15488583
|
T | TCA | 5 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1146_792+1147i others(4): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488583 | ||||||
chr1:15488609
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.792+1172T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488609 | ||||||
chr1:15488694
|
A | G | 5 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1257A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488694 | ||||||
chr1:15488789
|
G | A | 3 | a0004c0004t0001g0009a0004c0004t0001g0102a0006c0009t0001g0009 | 7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+1352G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488789 | ||||||
chr1:15488974
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0170 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.792+1537C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488974 | ||||||
chr1:15489055
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.792+1618A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489055 | ||||||
chr1:15489084
|
G | A | 87 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0066others(84): Show | 178 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.792+1647G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489084 | ||||||
chr1:15489107
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.792+1670C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489107 | ||||||
chr1:15489225
|
G | GTCCCAGC others(9): Show |
3 | a0004c0004t0001g0009a0004c0004t0001g0102a0006c0009t0001g0009 | 7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+1812_792+1827d others(18): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15489225 | |||||
chr1:15489304
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.792+1867C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489304 | ||||||
chr1:15489410
|
G | GT | 3 | a0004c0004t0001g0009a0004c0004t0001g0102a0006c0009t0001g0009 | 7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1884dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15489410 | |||||
chr1:15489427
|
G | A | 80 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0066others(77): Show | 169 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.793-1868G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489427 | ||||||
chr1:15489478
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.793-1817G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489478 | ||||||
chr1:15489487
|
G | A | 1 | a0002c0002t0001g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.793-1808G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489487 | ||||||
chr1:15489546
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.793-1749C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489546 | ||||||
chr1:15489570
|
A | C | 1 | a0001c0003t0001g0039 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-1725A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489570 | ||||||
chr1:15489726
|
A | T | 1 | a0002c0002t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.793-1569A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489726 | ||||||
chr1:15489800
|
G | A | 3 | a0004c0004t0001g0009a0004c0004t0001g0102a0006c0009t0001g0009 | 7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1495G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489800 | ||||||
chr1:15489937
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.793-1358G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489937 | ||||||
chr1:15490018
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793-1277C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490018 | ||||||
chr1:15490037
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.793-1258C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490037 | ||||||
chr1:15490067
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(31): Show | 77 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.793-1228T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490067 | ||||||
chr1:15490220
|
A | ATATC | 32 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0023others(29): Show | 68 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.793-1039_793-1036d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | |||||
chr1:15490220
|
A | ATATCTAT others(1): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0069others(4): Show | 13 | HG00544.hp1 HG00673.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.793-1043_793-1036d others(10): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | |||||
chr1:15490220
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A | ATATCTAT others(5): Show |
1 | a0002c0002t0001g0131 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.793-1047_793-1036d others(14): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | |||||
chr1:15490220
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ATATC | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0068 | 4 | HG02622.hp2 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1039_793-1036d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | |||||
chr1:15490220
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ATATCTAT others(1): Show |
A | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(35): Show | 87 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.793-1043_793-1036d others(10): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | |||||
chr1:15490220
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ATATCTAT others(9): Show |
A | 3 | a0001c0003t0001g0054a0001c0003t0001g0169a0001c0014t0001g0183 | 4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1051_793-1036d others(18): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | |||||
chr1:15490256
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CTATA | C | 4 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(1): Show | 4 | HG03540.hp2 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1036_793-1033d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490256 | |||||
chr1:15490258
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A | C | 1 | a0001c0001t0001g0151 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.793-1037A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490258 | ||||||
chr1:15490260
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A | C | 44 | a0001c0001t0001g0079a0001c0001t0001g0093a0001c0001t0001g0171others(41): Show | 81 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.793-1035A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490260 | ||||||
chr1:15490263
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C | T | 42 | a0001c0001t0001g0079a0001c0001t0001g0171a0002c0002t0001g0004others(39): Show | 78 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-1032C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490263 | ||||||
chr1:15490265
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C | T | 42 | a0001c0001t0001g0079a0001c0001t0001g0171a0002c0002t0001g0004others(39): Show | 78 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-1030C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490265 | ||||||
chr1:15490267
|
C | T | 1 | a0002c0002t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.793-1028C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490267 | ||||||
chr1:15490273
|
CACAT | C | 38 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0066others(35): Show | 91 | HG00140.hp1 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.793-1020_793-1017d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490273 | |||||
chr1:15490277
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T | C | 42 | a0001c0001t0001g0079a0001c0001t0001g0171a0002c0002t0001g0004others(39): Show | 78 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-1018T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490277 | ||||||
chr1:15490462
|
T | C | 3 | a0002c0002t0001g0040a0002c0002t0001g0107a0007c0012t0001g0040 | 3 | NA18939.hp2 NA18944.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.793-833T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490462 | ||||||
chr1:15490499
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C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0147a0001c0001t0001g0148 | 7 | NA18951.hp1 NA18954.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-796C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490499 | ||||||
chr1:15490547
|
G | A | 5 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-748G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490547 | ||||||
chr1:15490595
|
C | T | 75 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0066others(72): Show | 158 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.793-700C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490595 | ||||||
chr1:15490596
|
G | A | 1 | a0001c0003t0001g0039 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-699G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490596 | ||||||
chr1:15490638
|
C | T | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.793-657C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490638 | ||||||
chr1:15490682
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.793-613A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490682 | ||||||
chr1:15490737
|
G | T | 5 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-558G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490737 | ||||||
chr1:15490760
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.793-535C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490760 | ||||||
chr1:15490792
|
C | T | 1 | a0004c0004t0001g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.793-503C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490792 | ||||||
chr1:15490823
|
A | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(35): Show | 79 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.793-472A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490823 | ||||||
chr1:15490824
|
T | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(38): Show | 83 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.793-471T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490824 | ||||||
chr1:15490839
|
G | A | 78 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0066others(75): Show | 166 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.793-456G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490839 | ||||||
chr1:15490865
|
CA | C | 16 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0072others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.793-413delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490865 | |||||
chr1:15491002
|
G | A | 2 | a0001c0001t0001g0023a0002c0002t0001g0128 | 4 | HG01928.hp2 HG01975.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-293G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491002 | ||||||
chr1:15491012
|
C | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0166a0001c0007t0001g0053others(2): Show | 8 | HG00642.hp2 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-283C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491012 | ||||||
chr1:15491024
|
AG | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0016others(24): Show | 60 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.793-266delG | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15491024 | |||||
chr1:15491033
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0181 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.793-262G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491033 | ||||||
chr1:15491044
|
G | A | 2 | a0001c0001t0001g0167a0001c0003t0001g0039 | 3 | HG06807.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-251G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491044 | ||||||
chr1:15491045
|
A | C | 2 | a0001c0001t0001g0167a0001c0003t0001g0039 | 3 | HG06807.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-250A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491045 | ||||||
chr1:15491136
|
C | T | 3 | a0001c0001t0001g0066a0002c0002t0001g0045a0002c0002t0001g0129 | 4 | HG02132.hp2 NA18956.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-159C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491136 | ||||||
chr1:15491168
|
T | C | 1 | a0002c0002t0001g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.793-127T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491168 | ||||||
chr1:15491229
|
G | T | 3 | a0001c0007t0001g0053a0001c0007t0001g0143a0001c0007t0001g0164 | 4 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-66G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491229 |