geneid | 23436 |
---|---|
ensemblid | ENSG00000219073.8 |
hgncid | 15945 |
symbol | CELA3B |
name | chymotrypsin like elastase 3B |
refseq_nuc | NM_007352.4 |
refseq_prot | NP_031378.1 |
ensembl_nuc | ENST00000337107.11 |
ensembl_prot | ENSP00000338369.6 |
mane_status | MANE Select |
chr | chr1 |
start | 21977022 |
end | 21989354 |
strand | + |
ver | v1.2 |
region | chr1:21977022-21989354 |
region5000 | chr1:21972022-21994354 |
regionname0 | CELA3B_chr1_21977022_21989354 |
regionname5000 | CELA3B_chr1_21972022_21994354 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 7 | 4 | 1 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001 | 0/1 | 270 | 322 | 61 | 73 | 133 | 15 | 39 | 100 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002 | 1/0 | 270 | 86 | 24 | 2 | 55 | 1 | 3 | 43 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0003 | 0/0 | 270 | 9 | 0 | 0 | 6 | 0 | 3 | 5 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0004 | 0/0 | 270 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0005 | 0/0 | 270 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0006 | 0/0 | 270 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0007 | 0/0 | 270 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0008 | 0/0 | 270 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0009 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0010 | 0/0 | 270 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0011 | 0/0 | 270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0012 | 0/0 | 266 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0013 | 0/0 | 270 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0014 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 813 | 259 | 47 | 68 | 92 | 13 | 38 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0002 | 1/0 | 813 | 77 | 20 | 2 | 50 | 1 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0003 | 0/0 | 813 | 53 | 13 | 1 | 38 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0004 | 0/0 | 813 | 9 | 0 | 0 | 6 | 0 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0005 | 0/0 | 742 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0006 | 0/0 | 813 | 5 | 0 | 0 | 5 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0007 | 0/0 | 813 | 4 | 4 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0008 | 0/0 | 813 | 4 | 1 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0009 | 0/0 | 813 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0010 | 0/0 | 813 | 3 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0011 | 0/0 | 813 | 3 | 1 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0012 | 0/0 | 813 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0013 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0014 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0015 | 0/0 | 813 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0016 | 0/0 | 813 | 2 | 0 | 0 | 1 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0017 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0018 | 0/0 | 795 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0019 | 0/0 | 796 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0020 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0021 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0022 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0023 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0024 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
c0025 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 94 | 434 | 94 | 81 | 195 | 16 | 46 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
t0002 | 0/0 | 19 | 7 | 4 | 1 | 0 | 2 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
t0003 | 0/0 | 94 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
t0004 | 0/0 | 94 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 31 | 0 | 8 | 23 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0002 | 0/0 | 28 | 0 | 1 | 24 | 1 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0003 | 0/0 | 16 | 0 | 11 | 0 | 0 | 5 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0004 | 0/0 | 15 | 3 | 4 | 2 | 0 | 6 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0005 | 0/0 | 14 | 2 | 4 | 3 | 2 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0006 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0007 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0008 | 0/1 | 9 | 0 | 6 | 0 | 1 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0009 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0014 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0019 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0025 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0005 | 0/0 | 742 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0000c0018 | 0/0 | 795 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0000c0019 | 0/0 | 796 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0001 | 0/1 | 813 | 259 | 47 | 68 | 92 | 13 | 38 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0003 | 0/0 | 813 | 53 | 13 | 1 | 38 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0011 | 0/0 | 813 | 3 | 1 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0012 | 0/0 | 813 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0014 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0015 | 0/0 | 813 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0021 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0002 | 1/0 | 813 | 77 | 20 | 2 | 50 | 1 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0006 | 0/0 | 813 | 5 | 0 | 0 | 5 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0007 | 0/0 | 813 | 4 | 4 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0003c0004 | 0/0 | 813 | 9 | 0 | 0 | 6 | 0 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0004c0008 | 0/0 | 813 | 4 | 1 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0005c0009 | 0/0 | 813 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0006c0010 | 0/0 | 813 | 3 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0007c0016 | 0/0 | 813 | 2 | 0 | 0 | 1 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0008c0013 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0009c0017 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0010c0020 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0011c0024 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0012c0023 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0013c0025 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0014c0022 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0005t0002 | 0/0 | 760 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0000c0018t0002 | 0/0 | 813 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0000c0019t0002 | 0/0 | 814 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0001t0001 | 0/1 | 906 | 257 | 47 | 68 | 92 | 13 | 36 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0001t0003 | 0/0 | 906 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0003t0001 | 0/0 | 906 | 53 | 13 | 1 | 38 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0011t0001 | 0/0 | 906 | 3 | 1 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0012t0001 | 0/0 | 906 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0014t0001 | 0/0 | 906 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0015t0001 | 0/0 | 906 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0001c0021t0001 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0002t0001 | 1/0 | 906 | 77 | 20 | 2 | 50 | 1 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0006t0001 | 0/0 | 906 | 4 | 0 | 0 | 4 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0006t0004 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0002c0007t0001 | 0/0 | 906 | 4 | 4 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0003c0004t0001 | 0/0 | 906 | 9 | 0 | 0 | 6 | 0 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0004c0008t0001 | 0/0 | 906 | 4 | 1 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0005c0009t0001 | 0/0 | 906 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0006c0010t0001 | 0/0 | 906 | 3 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0007c0016t0001 | 0/0 | 906 | 2 | 0 | 0 | 1 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0008c0013t0001 | 0/0 | 906 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0009c0017t0001 | 0/0 | 906 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0010c0020t0001 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0011c0024t0001 | 0/0 | 906 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0012c0023t0001 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0013c0025t0001 | 0/0 | 906 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
a0014c0022t0001 | 0/0 | 906 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | copy fasta | chr1 | 21972022 | 21994354 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0005t0002g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0000c0005t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0000c0005t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0000c0005t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0000c0018t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0000c0019t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0001 | 0/0 | 31 | 0 | 8 | 23 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0003 | 0/0 | 13 | 0 | 9 | 0 | 0 | 4 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0004 | 0/0 | 15 | 3 | 4 | 2 | 0 | 6 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0005 | 0/0 | 14 | 2 | 4 | 3 | 2 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0007 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0008 | 0/1 | 6 | 0 | 4 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0019 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0006 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0009 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0011t0001g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0012t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0014t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0015t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0015t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0001c0021t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0002 | 0/0 | 28 | 0 | 1 | 24 | 1 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0006t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0007t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0002c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0003c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0004c0008t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0004c0008t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0004c0008t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0005c0009t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0006c0010t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0006c0010t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0006c0010t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0007c0016t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0007c0016t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0008c0013t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0009c0017t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0010c0020t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0011c0024t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0012c0023t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0013c0025t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
a0014c0022t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0073 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00280 | hp1 | a0001 | c0012 | t0001 | g0008 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0132 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00558 | hp2 | a0002 | c0006 | t0001 | g0146 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00609 | hp1 | a0010 | c0020 | t0001 | g0209 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00735 | hp2 | a0004 | c0008 | t0001 | g0027 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01069 | hp1 | a0001 | c0011 | t0001 | g0024 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01071 | hp1 | a0001 | c0011 | t0001 | g0024 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01109 | hp2 | a0001 | c0015 | t0001 | g0008 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0215 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01175 | hp1 | a0001 | c0012 | t0001 | g0008 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01243 | hp1 | a0000 | c0005 | t0002 | g0046 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01243 | hp2 | a0004 | c0008 | t0001 | g0061 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01255 | hp1 | a0004 | c0008 | t0001 | g0027 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01346 | hp2 | a0005 | c0009 | t0001 | g0003 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01496 | hp1 | a0005 | c0009 | t0001 | g0003 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01515 | hp2 | a0000 | c0019 | t0002 | g0174 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01517 | hp1 | a0000 | c0018 | t0002 | g0173 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01891 | hp1 | a0006 | c0010 | t0001 | g0176 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02004 | hp2 | a0013 | c0025 | t0001 | g0078 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02040 | hp1 | a0003 | c0004 | t0001 | g0038 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02056 | hp2 | a0001 | c0014 | t0001 | g0014 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02074 | hp1 | a0001 | c0014 | t0001 | g0014 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02135 | hp2 | a0007 | c0016 | t0001 | g0069 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02145 | hp2 | a0008 | c0013 | t0001 | g0011 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02257 | hp2 | a0000 | c0005 | t0002 | g0046 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02280 | hp1 | a0002 | c0007 | t0001 | g0045 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02572 | hp2 | a0002 | c0007 | t0001 | g0165 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02630 | hp1 | a0006 | c0010 | t0001 | g0175 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02886 | hp2 | a0009 | c0017 | t0001 | g0170 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02970 | hp2 | a0008 | c0013 | t0001 | g0011 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02976 | hp1 | a0012 | c0023 | t0001 | g0214 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03017 | hp1 | a0007 | c0016 | t0001 | g0097 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03098 | hp1 | a0000 | c0005 | t0002 | g0167 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03139 | hp2 | a0000 | c0005 | t0002 | g0168 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03491 | hp2 | a0003 | c0004 | t0001 | g0121 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03540 | hp2 | a0001 | c0011 | t0001 | g0024 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03579 | hp2 | a0006 | c0010 | t0001 | g0056 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03654 | hp1 | a0011 | c0024 | t0001 | g0186 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03704 | hp2 | a0003 | c0004 | t0001 | g0116 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03710 | hp2 | a0001 | c0015 | t0001 | g0179 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03834 | hp1 | a0003 | c0004 | t0001 | g0122 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04204 | hp1 | a0005 | c0009 | t0001 | g0003 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18522 | hp1 | a0004 | c0008 | t0001 | g0062 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18522 | hp2 | a0000 | c0005 | t0002 | g0169 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18947 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18954 | hp1 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18962 | hp1 | a0003 | c0004 | t0001 | g0135 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18963 | hp1 | a0001 | c0021 | t0001 | g0029 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18965 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18975 | hp1 | a0003 | c0004 | t0001 | g0038 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18978 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18984 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18987 | hp1 | a0002 | c0006 | t0001 | g0152 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18990 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18997 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18999 | hp2 | a0003 | c0004 | t0001 | g0125 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19054 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19055 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19058 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19060 | hp1 | a0002 | c0006 | t0001 | g0043 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19074 | hp1 | a0003 | c0004 | t0001 | g0112 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19077 | hp1 | a0002 | c0006 | t0001 | g0148 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19082 | hp1 | a0002 | c0006 | t0004 | g0043 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | ASW | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02109 | hp2 | a0002 | c0007 | t0001 | g0045 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02486 | hp2 | a0014 | c0022 | t0001 | g0109 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
NA21309 | hp2 | a0002 | c0007 | t0001 | g0166 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0164 | REF | REF | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21978396
|
G | A | 1 | a0005 | 3 | HG01346.hp2 HG01496.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.71G>A | p.Arg24His | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/8 | 89/906 | 71/813 | 24/270 | chr1 | 21978396 | ||
chr1:21978398
|
C | T | 1 | a0005 | 3 | HG01346.hp2 HG01496.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.73C>T | p.Pro25Ser | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/8 | 91/906 | 73/813 | 25/270 | chr1 | 21978398 | ||
chr1:21978416
|
A | C | 2 | a0005a0007 | 5 | HG01346.hp2 HG01496.hp1 HG02135.hp2 others(2): Show |
missense_variant | MODERATE | c.91A>C | p.Asn31His | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/8 | 109/906 | 91/813 | 31/270 | chr1 | 21978416 | ||
chr1:21981045
|
C | T | 13 | a0000a0001a0003others(10): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
missense_variant | MODERATE | c.235C>T | p.Arg79Trp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/8 | 253/906 | 235/813 | 79/270 | chr1 | 21981045 | ||
chr1:21981049
|
C | A | 1 | a0010 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.239C>A | p.Thr80Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/8 | 257/906 | 239/813 | 80/270 | chr1 | 21981049 | ||
chr1:21981089
|
G | T | 1 | a0008 | 2 | HG02145.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.279G>T | p.Lys93Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/8 | 297/906 | 279/813 | 93/270 | chr1 | 21981089 | ||
chr1:21983722
|
C | T | 1 | a0003 | 9 | HG02040.hp1 HG03491.hp2 HG03704.hp2 others(6): Show |
missense_variant | MODERATE | c.391C>T | p.Arg131Cys | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 409/906 | 391/813 | 131/270 | chr1 | 21983722 | ||
chr1:21983732
|
A | T | 1 | a0004 | 4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
missense_variant | MODERATE | c.401A>T | p.Gln134Leu | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 419/906 | 401/813 | 134/270 | chr1 | 21983732 | ||
chr1:21984218
|
G | C | 1 | a0009 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.529G>C | p.Glu177Gln | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 547/906 | 529/813 | 177/270 | chr1 | 21984218 | ||
chr1:21984278
|
T | A | 1 | a0014 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.589T>A | p.Ser197Thr | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 607/906 | 589/813 | 197/270 | chr1 | 21984278 | ||
chr1:21984314
|
A | G | 1 | a0013 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.625A>G | p.Ile209Val | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 643/906 | 625/813 | 209/270 | chr1 | 21984314 | ||
chr1:21984318
|
G | A | 2 | a0000a0006 | 5 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
missense_variant | MODERATE | c.629G>A | p.Arg210His | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 647/906 | 629/813 | 210/270 | chr1 | 21984318 | ||
chr1:21986599
|
C | CTTTGTTT others(12): Show |
1 | a0012 | 1 | HG02976.hp1 | frameshift_variant | HIGH | c.725_726insCAGCTTTT others(11): Show |
p.Gly243fs | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/8 | 744/906 | 726/813 | 242/270 | INFO_REALIGN_3_PRIME | chr1 | 21986599 | |
chr1:21986610
|
C | G | 1 | a0000 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.722C>G | p.Ala241Gly | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/8 | 740/906 | 722/813 | 241/270 | chr1 | 21986610 | ||
chr1:21986630
|
AGGAAGCC others(7717): Show |
A | 1 | a0000 | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
exon_loss_variant | HIGH | c.743_*5075del | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 761/906 | chr1 | 21986630 | |||||
chr1:21989153
|
TCCTCTCC others(5194): Show |
T | 1 | a0000 | 1 | HG01517.hp1 | exon_loss_variant&splice_acceptor_variant&3_prime_UTR_truncation&exon_loss_variant&splice_region_variant&intron_variant | HIGH | c.796-103_*5080del | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 21989153 | |||||
chr1:21989262
|
ACCATAGC others(5085): Show |
A | 1 | a0000 | 1 | HG01515.hp2 | stop_lost&3_prime_UTR_truncation&exon_loss_variant&conservative_inframe_deletion&splice_region_variant | HIGH | c.799_*5077del | p.Ile267_Ter271del | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 817/906 | 799/813 | 267/270 | INFO_REALIGN_3_PRIME | chr1 | 21989262 | |
chr1:21989266
|
T | C | 1 | a0011 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.800T>C | p.Ile267Thr | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 818/906 | 800/813 | 267/270 | chr1 | 21989266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21980847
|
C | T | 16 | a0001c0001a0001c0003a0001c0011others(13): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
synonymous_variant | LOW | c.153C>T | p.Ser51Ser | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 171/906 | 153/813 | 51/270 | chr1 | 21980847 | ||
chr1:21980865
|
C | G | 16 | a0001c0001a0001c0003a0001c0011others(13): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
synonymous_variant | LOW | c.171C>G | p.Thr57Thr | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 189/906 | 171/813 | 57/270 | chr1 | 21980865 | ||
chr1:21980883
|
C | T | 1 | a0001c0015 | 2 | HG01109.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.189C>T | p.Ile63Ile | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 207/906 | 189/813 | 63/270 | chr1 | 21980883 | ||
chr1:21980892
|
C | T | 1 | a0001c0014 | 2 | HG02056.hp2 HG02074.hp1 |
synonymous_variant | LOW | c.198C>T | p.Asp66Asp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 216/906 | 198/813 | 66/270 | chr1 | 21980892 | ||
chr1:21983697
|
T | C | 2 | a0001c0003a0001c0021 | 54 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.366T>C | p.Asn122Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 384/906 | 366/813 | 122/270 | chr1 | 21983697 | ||
chr1:21983742
|
C | T | 1 | a0002c0007 | 4 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(1): Show |
synonymous_variant | LOW | c.411C>T | p.Asp137Asp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 429/906 | 411/813 | 137/270 | chr1 | 21983742 | ||
chr1:21983769
|
G | C | 19 | a0000c0018a0000c0019a0001c0001others(16): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
synonymous_variant | LOW | c.438G>C | p.Pro146Pro | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 456/906 | 438/813 | 146/270 | chr1 | 21983769 | ||
chr1:21983790
|
C | T | 1 | a0001c0021 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.459C>T | p.Asn153Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 477/906 | 459/813 | 153/270 | chr1 | 21983790 | ||
chr1:21984208
|
C | T | 1 | a0001c0012 | 2 | HG00280.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.519C>T | p.Asp173Asp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 537/906 | 519/813 | 173/270 | chr1 | 21984208 | ||
chr1:21984232
|
G | C | 15 | a0001c0001a0001c0003a0001c0011others(12): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
synonymous_variant | LOW | c.543G>C | p.Pro181Pro | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 561/906 | 543/813 | 181/270 | chr1 | 21984232 | ||
chr1:21984331
|
T | C | 20 | a0000c0018a0000c0019a0001c0001others(17): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
splice_region_variant&synonymous_variant | LOW | c.642T>C | p.Asn214Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 660/906 | 642/813 | 214/270 | chr1 | 21984331 | ||
chr1:21986668
|
T | C | 18 | a0000c0018a0000c0019a0001c0001others(15): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
synonymous_variant | LOW | c.780T>C | p.Ile260Ile | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/8 | 798/906 | 780/813 | 260/270 | chr1 | 21986668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21989302
|
C | T | 1 | a0001c0001t0003 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*23C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 23 | chr1 | 21989302 | |||||
chr1:21989307
|
C | T | 1 | a0002c0006t0004 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 28 | chr1 | 21989307 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21977092
|
C | A | 1 | a0006c0010t0001g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.43+10C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977092 | ||||||
chr1:21977100
|
G | C | 8 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(5): Show | 10 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+18G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977100 | ||||||
chr1:21977209
|
C | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(105): Show | 201 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43+127C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977209 | ||||||
chr1:21977226
|
G | A | 1 | a0002c0002t0001g0016 | 5 | HG02109.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+144G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977226 | ||||||
chr1:21977339
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.43+257G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977339 | ||||||
chr1:21977353
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+271G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977353 | ||||||
chr1:21977354
|
C | A | 1 | a0001c0001t0001g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.43+272C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977354 | ||||||
chr1:21977428
|
C | G | 39 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(36): Show | 53 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.43+346C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977428 | ||||||
chr1:21977474
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 6 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+392G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977474 | ||||||
chr1:21977511
|
G | A | 2 | a0001c0001t0001g0140a0014c0022t0001g0109 | 2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.43+429G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977511 | ||||||
chr1:21977603
|
T | C | 1 | a0002c0002t0001g0141 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.43+521T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977603 | ||||||
chr1:21977649
|
T | A | 25 | a0001c0001t0001g0028a0001c0003t0001g0006a0001c0003t0001g0013others(22): Show | 44 | HG00140.hp2 HG00597.hp2 HG02004.hp2 others(41): Show |
intron_variant | MODIFIER | c.43+567T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977649 | ||||||
chr1:21977736
|
T | C | 24 | a0001c0001t0001g0028a0001c0003t0001g0006a0001c0003t0001g0013others(21): Show | 43 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.44-633T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977736 | ||||||
chr1:21977771
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.44-598C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977771 | ||||||
chr1:21977779
|
G | T | 73 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0004others(70): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.44-590G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977779 | ||||||
chr1:21977790
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(84): Show | 162 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.44-579T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977790 | ||||||
chr1:21977914
|
GC | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(83): Show | 161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.44-452delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 21977914 | |||||
chr1:21977935
|
C | G | 191 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(188): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.44-434C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977935 | ||||||
chr1:21977936
|
C | T | 191 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(188): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.44-433C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977936 | ||||||
chr1:21977938
|
G | C | 24 | a0001c0001t0001g0028a0001c0003t0001g0006a0001c0003t0001g0013others(21): Show | 43 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.44-431G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977938 | ||||||
chr1:21977961
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.44-408G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977961 | ||||||
chr1:21977970
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.44-399A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977970 | ||||||
chr1:21978092
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 221 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.44-277T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978092 | ||||||
chr1:21978175
|
G | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(83): Show | 161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.44-194G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978175 | ||||||
chr1:21978178
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(83): Show | 161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.44-191T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978178 | ||||||
chr1:21978219
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(88): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.44-150A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978219 | ||||||
chr1:21978248
|
G | A | 1 | a0001c0001t0001g0047 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.44-121G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978248 | ||||||
chr1:21978290
|
C | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(38): Show | 55 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.44-79C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978290 | ||||||
chr1:21978297
|
G | C | 1 | a0001c0001t0003g0031 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.44-72G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978297 | ||||||
chr1:21978338
|
C | A | 59 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0028others(56): Show | 92 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.44-31C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978338 | ||||||
chr1:21978487
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.129+33C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978487 | ||||||
chr1:21978519
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.129+65G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978519 | ||||||
chr1:21978604
|
C | T | 3 | a0002c0007t0001g0045a0002c0007t0001g0165a0002c0007t0001g0166 | 4 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+150C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978604 | ||||||
chr1:21978605
|
G | A | 28 | a0001c0001t0001g0136a0001c0001t0001g0137a0002c0002t0001g0002others(25): Show | 67 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.129+151G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978605 | ||||||
chr1:21978635
|
C | G | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.129+181C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978635 | ||||||
chr1:21978661
|
G | T | 1 | a0001c0003t0001g0041 | 2 | NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.129+207G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978661 | ||||||
chr1:21978682
|
A | G | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.129+228A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978682 | ||||||
chr1:21978722
|
C | A | 5 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(2): Show | 6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+268C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978722 | ||||||
chr1:21978737
|
A | C | 1 | a0006c0010t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.129+283A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978737 | ||||||
chr1:21978784
|
A | T | 1 | a0002c0002t0001g0159 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.129+330A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978784 | ||||||
chr1:21978793
|
A | T | 1 | a0002c0002t0001g0159 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.129+339A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978793 | ||||||
chr1:21978796
|
G | A | 1 | a0002c0002t0001g0159 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.129+342G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978796 | ||||||
chr1:21978825
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+371T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978825 | ||||||
chr1:21978857
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+403G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978857 | ||||||
chr1:21978874
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.129+420G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978874 | ||||||
chr1:21978903
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.129+449C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978903 | ||||||
chr1:21978909
|
C | T | 5 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(2): Show | 6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+455C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978909 | ||||||
chr1:21979001
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.129+547C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979001 | ||||||
chr1:21979014
|
T | A | 1 | a0001c0001t0001g0048 | 2 | HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.129+560T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979014 | ||||||
chr1:21979047
|
C | CA | 184 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(181): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.129+602dupA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979047 | |||||
chr1:21979133
|
C | T | 185 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(182): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.129+679C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979133 | ||||||
chr1:21979134
|
A | G | 185 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(182): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.129+680A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979134 | ||||||
chr1:21979135
|
C | T | 185 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(182): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.129+681C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979135 | ||||||
chr1:21979136
|
A | G | 185 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(182): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.129+682A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979136 | ||||||
chr1:21979144
|
C | T | 1 | a0002c0007t0001g0045 | 2 | HG02109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.129+690C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979144 | ||||||
chr1:21979158
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+704T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979158 | ||||||
chr1:21979159
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(42): Show | 106 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.129+705G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979159 | ||||||
chr1:21979165
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.129+711C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979165 | ||||||
chr1:21979215
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+761G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979215 | ||||||
chr1:21979219
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+765T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979219 | ||||||
chr1:21979232
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.129+778C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979232 | ||||||
chr1:21979241
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(52): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.129+787T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979241 | ||||||
chr1:21979298
|
G | T | 8 | a0000c0018t0002g0173a0000c0019t0002g0174a0004c0008t0001g0027others(5): Show | 9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+844G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979298 | ||||||
chr1:21979352
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 10 | HG00609.hp1 HG03041.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+898G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979352 | ||||||
chr1:21979372
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(5): Show | 24 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.129+918G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979372 | ||||||
chr1:21979394
|
T | C | 1 | a0002c0002t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129+940T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979394 | ||||||
chr1:21979413
|
C | T | 8 | a0000c0018t0002g0173a0000c0019t0002g0174a0004c0008t0001g0027others(5): Show | 9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+959C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979413 | ||||||
chr1:21979415
|
G | A | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+961G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979415 | ||||||
chr1:21979422
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(52): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.129+968C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979422 | ||||||
chr1:21979443
|
CTTTTCTT others(6): Show |
C | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.129+994_129+1006de others(14): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979443 | |||||
chr1:21979446
|
TTCTTTTC | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0113others(3): Show | 6 | HG02055.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+994_129+1000de others(8): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979446 | |||||
chr1:21979447
|
TCTTTTC | T | 32 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0037others(29): Show | 45 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.129+994_129+999del others(6): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979447 | ||||||
chr1:21979448
|
CTTTTCT | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0180a0001c0001t0001g0210others(2): Show | 11 | HG00609.hp1 HG03041.hp1 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+999_129+1004de others(7): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979448 | |||||
chr1:21979448
|
CTTTTCTT others(7): Show |
C | 1 | a0001c0001t0001g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.129+999_129+1012de others(15): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979448 | |||||
chr1:21979449
|
TTTTC | T | 5 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(2): Show | 6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+999_129+1002de others(5): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979449 | |||||
chr1:21979450
|
TTTC | T | 7 | a0001c0001t0001g0028a0001c0003t0001g0013a0001c0003t0001g0067others(4): Show | 13 | HG02080.hp2 HG02135.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.129+999_129+1001de others(4): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979450 | |||||
chr1:21979451
|
TTC | T | 13 | a0001c0001t0001g0082a0001c0003t0001g0006a0001c0003t0001g0029others(10): Show | 25 | HG00140.hp2 HG00597.hp2 NA18950.hp1 others(22): Show |
intron_variant | MODIFIER | c.129+999_129+1000de others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979451 | |||||
chr1:21979452
|
TC | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(38): Show | 102 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.129+999delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979452 | ||||||
chr1:21979453
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 5 | HG02004.hp2 HG03195.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+999C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979453 | ||||||
chr1:21979453
|
CT | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.129+1016delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979453 | |||||
chr1:21979453
|
CTT | C | 12 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(9): Show | 13 | HG00597.hp1 HG01167.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+1015_129+1016d others(4): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979453 | |||||
chr1:21979453
|
CTTT | C | 6 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0181others(3): Show | 7 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1014_129+1016d others(5): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979453 | |||||
chr1:21979468
|
T | G | 1 | a0002c0002t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129+1014T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979468 | ||||||
chr1:21979477
|
G | A | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.129+1023G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979477 | ||||||
chr1:21979478
|
G | A | 1 | a0003c0004t0001g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.129+1024G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979478 | ||||||
chr1:21979516
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+1062A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979516 | ||||||
chr1:21979549
|
T | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+1095T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979549 | ||||||
chr1:21979551
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+1097C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979551 | ||||||
chr1:21979558
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.129+1104T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979558 | ||||||
chr1:21979566
|
C | T | 1 | a0001c0001t0001g0055 | 2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.129+1112C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979566 | ||||||
chr1:21979601
|
T | C | 185 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(182): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.129+1147T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979601 | ||||||
chr1:21979666
|
C | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.130-1158C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979666 | ||||||
chr1:21979700
|
T | C | 193 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(190): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.130-1124T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979700 | ||||||
chr1:21979715
|
C | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.130-1109C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979715 | ||||||
chr1:21979743
|
C | T | 19 | a0001c0001t0001g0028a0001c0003t0001g0006a0001c0003t0001g0013others(16): Show | 37 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(34): Show |
intron_variant | MODIFIER | c.130-1081C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979743 | ||||||
chr1:21979855
|
C | T | 8 | a0000c0018t0002g0173a0000c0019t0002g0174a0004c0008t0001g0027others(5): Show | 9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.130-969C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979855 | ||||||
chr1:21979885
|
T | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-939T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979885 | ||||||
chr1:21979978
|
A | G | 2 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-846A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979978 | ||||||
chr1:21979988
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.130-836G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979988 | ||||||
chr1:21980014
|
A | AC | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-810_130-809ins others(1): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980014 | ||||||
chr1:21980015
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.130-809A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980015 | ||||||
chr1:21980040
|
C | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.130-784C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980040 | ||||||
chr1:21980059
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-765C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980059 | ||||||
chr1:21980062
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-762A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980062 | ||||||
chr1:21980131
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130-693C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980131 | ||||||
chr1:21980134
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0064others(7): Show | 18 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.130-690G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980134 | ||||||
chr1:21980195
|
G | C | 2 | a0001c0003t0001g0067a0001c0003t0001g0071 | 2 | NA18986.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.130-629G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980195 | ||||||
chr1:21980210
|
T | G | 1 | a0011c0024t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130-614T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980210 | ||||||
chr1:21980217
|
C | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0028others(61): Show | 97 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.130-607C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980217 | ||||||
chr1:21980240
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(5): Show | 24 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-584G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980240 | ||||||
chr1:21980277
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.130-547C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980277 | ||||||
chr1:21980297
|
T | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(35): Show | 51 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.130-527T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980297 | ||||||
chr1:21980309
|
G | C | 3 | a0002c0002t0001g0042a0002c0002t0001g0145a0002c0002t0001g0157 | 4 | HG02083.hp2 NA19067.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-515G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980309 | ||||||
chr1:21980316
|
C | T | 24 | a0001c0001t0001g0028a0001c0003t0001g0006a0001c0003t0001g0013others(21): Show | 43 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.130-508C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980316 | ||||||
chr1:21980330
|
T | C | 2 | a0002c0002t0001g0018a0009c0017t0001g0170 | 6 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-494T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980330 | ||||||
chr1:21980339
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.130-485C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980339 | ||||||
chr1:21980344
|
C | T | 1 | a0001c0003t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.130-480C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980344 | ||||||
chr1:21980345
|
G | C | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.130-479G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980345 | ||||||
chr1:21980364
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130-460A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980364 | ||||||
chr1:21980376
|
G | A | 1 | a0002c0002t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.130-448G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980376 | ||||||
chr1:21980456
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(43): Show | 108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.130-368G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980456 | ||||||
chr1:21980462
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-362A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980462 | ||||||
chr1:21980465
|
A | G | 1 | a0002c0007t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130-359A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980465 | ||||||
chr1:21980484
|
C | A | 2 | a0002c0002t0001g0143a0002c0006t0001g0146 | 2 | HG00558.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.130-340C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980484 | ||||||
chr1:21980492
|
G | C | 2 | a0002c0002t0001g0143a0002c0006t0001g0146 | 2 | HG00558.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.130-332G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980492 | ||||||
chr1:21980510
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(7): Show | 28 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.130-314C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980510 | ||||||
chr1:21980511
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(7): Show | 28 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.130-313G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980511 | ||||||
chr1:21980539
|
C | G | 63 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0004others(60): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.130-285C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980539 | ||||||
chr1:21980541
|
C | T | 63 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0004others(60): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.130-283C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980541 | ||||||
chr1:21980546
|
A | G | 63 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0004others(60): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.130-278A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980546 | ||||||
chr1:21980567
|
G | C | 5 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(2): Show | 6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-257G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980567 | ||||||
chr1:21980589
|
G | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.130-235G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980589 | ||||||
chr1:21980666
|
A | G | 1 | a0001c0015t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.130-158A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980666 | ||||||
chr1:21980692
|
TC | T | 1 | a0001c0001t0001g0021 | 3 | HG00673.hp1 HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.130-131delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980692 | ||||||
chr1:21980696
|
T | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(36): Show | 84 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.130-128T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980696 | ||||||
chr1:21980706
|
T | C | 44 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(41): Show | 60 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.130-118T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980706 | ||||||
chr1:21980713
|
C | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(82): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.130-111C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980713 | ||||||
chr1:21980714
|
G | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(127): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.130-110G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980714 | ||||||
chr1:21980723
|
G | C | 2 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-101G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980723 | ||||||
chr1:21980730
|
C | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0037others(25): Show | 37 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.130-94C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980730 | ||||||
chr1:21980759
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(43): Show | 108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.130-65G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980759 | ||||||
chr1:21980985
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.228-53G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/7 | chr1 | 21980985 | ||||||
chr1:21981030
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18990.hp1 | splice_region_variant&intron_variant | LOW | c.228-8G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/7 | chr1 | 21981030 | ||||||
chr1:21981183
|
G | C | 1 | a0001c0011t0001g0024 | 3 | HG01069.hp1 HG01071.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362+11G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981183 | ||||||
chr1:21981187
|
C | T | 2 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.362+15C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981187 | ||||||
chr1:21981215
|
C | T | 20 | a0001c0003t0001g0006a0001c0003t0001g0009a0001c0003t0001g0029others(17): Show | 40 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.362+43C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981215 | ||||||
chr1:21981216
|
A | G | 20 | a0001c0003t0001g0006a0001c0003t0001g0009a0001c0003t0001g0029others(17): Show | 40 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.362+44A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981216 | ||||||
chr1:21981250
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+78T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981250 | ||||||
chr1:21981262
|
G | GTAGGACG others(8): Show |
1 | a0001c0001t0001g0105 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.362+91_362+92insAG others(13): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981262 | |||||
chr1:21981264
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+92T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981264 | ||||||
chr1:21981270
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.362+98G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981270 | ||||||
chr1:21981270
|
G | GTAGGGAC others(9): Show |
175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+105_362+106ins others(16): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981270 | |||||
chr1:21981278
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.362+106G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981278 | ||||||
chr1:21981288
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+116G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981288 | ||||||
chr1:21981336
|
A | C | 188 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(185): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.362+164A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981336 | ||||||
chr1:21981382
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+210G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981382 | ||||||
chr1:21981406
|
C | T | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.362+234C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981406 | ||||||
chr1:21981422
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(7): Show | 28 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.362+250G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981422 | ||||||
chr1:21981475
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.362+303A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981475 | ||||||
chr1:21981477
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.362+305G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981477 | ||||||
chr1:21981479
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.362+307C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981479 | ||||||
chr1:21981543
|
C | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0047others(8): Show | 29 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.362+371C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981543 | ||||||
chr1:21981667
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+495C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981667 | ||||||
chr1:21981671
|
C | T | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.362+499C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981671 | ||||||
chr1:21981672
|
G | T | 19 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0014others(16): Show | 25 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.362+500G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981672 | ||||||
chr1:21981685
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.362+513G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981685 | ||||||
chr1:21981691
|
G | A | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.362+519G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981691 | ||||||
chr1:21981720
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+548A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981720 | ||||||
chr1:21981728
|
CT | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.362+571delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981728 | |||||
chr1:21981728
|
CTT | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0117others(5): Show | 13 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.362+570_362+571del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981728 | |||||
chr1:21981842
|
C | T | 1 | a0003c0004t0001g0114 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.362+670C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981842 | ||||||
chr1:21981870
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.362+698C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981870 | ||||||
chr1:21981875
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.362+703G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981875 | ||||||
chr1:21981919
|
G | A | 1 | a0010c0020t0001g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.362+747G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981919 | ||||||
chr1:21981927
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.362+755G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981927 | ||||||
chr1:21981938
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.362+766G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981938 | ||||||
chr1:21981942
|
A | G | 20 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0001t0001g0118others(17): Show | 21 | HG00099.hp2 HG00438.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.362+770A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981942 | ||||||
chr1:21981946
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.362+774C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981946 | ||||||
chr1:21981947
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0086a0001c0003t0001g0026others(5): Show | 9 | HG02300.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.362+775G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981947 | ||||||
chr1:21981960
|
C | T | 3 | a0001c0001t0001g0108a0002c0002t0001g0018a0009c0017t0001g0170 | 7 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+788C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981960 | ||||||
chr1:21981967
|
T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(1): Show | 4 | HG02056.hp1 HG03017.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+795T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981967 | ||||||
chr1:21981976
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.362+804C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981976 | ||||||
chr1:21981993
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.362+821A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981993 | ||||||
chr1:21982000
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.362+828C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982000 | ||||||
chr1:21982005
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0108a0001c0001t0001g0182others(1): Show | 8 | HG00738.hp1 HG01167.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.362+833A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982005 | ||||||
chr1:21982016
|
C | T | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.362+844C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982016 | ||||||
chr1:21982023
|
C | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+851C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982023 | ||||||
chr1:21982054
|
A | C | 184 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(181): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.362+882A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982054 | ||||||
chr1:21982095
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.362+923G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982095 | ||||||
chr1:21982148
|
G | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.362+976G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982148 | ||||||
chr1:21982163
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.362+991C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982163 | ||||||
chr1:21982179
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362+1007G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982179 | ||||||
chr1:21982211
|
A | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.362+1039A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982211 | ||||||
chr1:21982215
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.362+1043G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982215 | ||||||
chr1:21982217
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.362+1045C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982217 | ||||||
chr1:21982279
|
C | T | 1 | a0003c0004t0001g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.362+1107C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982279 | ||||||
chr1:21982301
|
G | A | 1 | a0002c0002t0001g0150 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.362+1129G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982301 | ||||||
chr1:21982314
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.362+1142A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982314 | ||||||
chr1:21982360
|
C | T | 11 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0003t0001g0026others(8): Show | 13 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.362+1188C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982360 | ||||||
chr1:21982439
|
TA | T | 184 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(181): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.363-1247delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21982439 | |||||
chr1:21982440
|
A | T | 2 | a0000c0005t0002g0046a0000c0005t0002g0169 | 3 | HG01243.hp1 HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.363-1254A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982440 | ||||||
chr1:21982441
|
A | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(9): Show | 31 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.363-1253A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982441 | ||||||
chr1:21982465
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.363-1229C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982465 | ||||||
chr1:21982490
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(46): Show | 111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.363-1204T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982490 | ||||||
chr1:21982498
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.363-1196G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982498 | ||||||
chr1:21982545
|
C | T | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-1149C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982545 | ||||||
chr1:21982596
|
C | CA | 184 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(181): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.363-1089dupA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21982596 | |||||
chr1:21982771
|
A | G | 39 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(36): Show | 53 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.363-923A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982771 | ||||||
chr1:21982791
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.363-903C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982791 | ||||||
chr1:21982803
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.363-891G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982803 | ||||||
chr1:21982827
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-867G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982827 | ||||||
chr1:21982844
|
AT | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-842delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21982844 | |||||
chr1:21982944
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(7): Show | 27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-750C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982944 | ||||||
chr1:21982973
|
G | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-721G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982973 | ||||||
chr1:21983075
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.363-619C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983075 | ||||||
chr1:21983077
|
C | T | 184 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(181): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.363-617C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983077 | ||||||
chr1:21983121
|
G | A | 3 | a0004c0008t0001g0027a0004c0008t0001g0061a0004c0008t0001g0062 | 4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-573G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983121 | ||||||
chr1:21983197
|
T | A | 184 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(181): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.363-497T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983197 | ||||||
chr1:21983213
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-481A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983213 | ||||||
chr1:21983216
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-478G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983216 | ||||||
chr1:21983232
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.363-462G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983232 | ||||||
chr1:21983312
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(9): Show | 31 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.363-382G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983312 | ||||||
chr1:21983315
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(45): Show | 110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.363-379A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983315 | ||||||
chr1:21983354
|
CA | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-329delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983354 | |||||
chr1:21983374
|
T | A | 8 | a0000c0018t0002g0173a0000c0019t0002g0174a0004c0008t0001g0027others(5): Show | 9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-320T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983374 | ||||||
chr1:21983381
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-313T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983381 | ||||||
chr1:21983392
|
C | T | 1 | a0002c0002t0001g0044 | 2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.363-302C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983392 | ||||||
chr1:21983445
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-249T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983445 | ||||||
chr1:21983464
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.363-230T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983464 | ||||||
chr1:21983524
|
T | C | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.363-170T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983524 | ||||||
chr1:21983525
|
G | C | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.363-169G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983525 | ||||||
chr1:21983548
|
A | AATG | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-129_363-127dup others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983548 | |||||
chr1:21983548
|
A | AATGATGA others(2): Show |
3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.363-135_363-127dup others(9): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983548 | |||||
chr1:21983548
|
A | AATGATGA others(5): Show |
2 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.363-138_363-127dup others(12): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983548 | |||||
chr1:21983587
|
G | A | 181 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(178): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.363-107G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983587 | ||||||
chr1:21983634
|
G | A | 6 | a0004c0008t0001g0027a0004c0008t0001g0061a0004c0008t0001g0062others(3): Show | 7 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-60G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983634 | ||||||
chr1:21983646
|
T | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-48T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983646 | ||||||
chr1:21983652
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.363-42C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983652 | ||||||
chr1:21983671
|
C | T | 1 | a0002c0002t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.363-23C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983671 | ||||||
chr1:21983911
|
C | T | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+81C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983911 | ||||||
chr1:21983918
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.499+88A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983918 | ||||||
chr1:21983920
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.499+90A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983920 | ||||||
chr1:21983973
|
C | G | 1 | a0002c0002t0001g0154 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.499+143C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983973 | ||||||
chr1:21983977
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.499+147A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983977 | ||||||
chr1:21983981
|
C | T | 1 | a0001c0003t0001g0030 | 2 | NA18990.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.499+151C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983981 | ||||||
chr1:21984014
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.500-175T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984014 | ||||||
chr1:21984026
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(7): Show | 27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.500-163G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984026 | ||||||
chr1:21984049
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0120 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.500-140A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984049 | ||||||
chr1:21984095
|
A | G | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-94A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984095 | ||||||
chr1:21984113
|
C | T | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.500-76C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984113 | ||||||
chr1:21984168
|
C | A | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.500-21C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984168 | ||||||
chr1:21984169
|
G | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.500-20G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984169 | ||||||
chr1:21984181
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
splice_region_variant&intron_variant | LOW | c.500-8C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984181 | ||||||
chr1:21984354
|
G | C | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642+23G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984354 | ||||||
chr1:21984440
|
C | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.642+109C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984440 | ||||||
chr1:21984502
|
G | C | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+171G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984502 | ||||||
chr1:21984518
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.642+187G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984518 | ||||||
chr1:21984544
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(3): Show | 9 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+213A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984544 | ||||||
chr1:21984566
|
G | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(125): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.642+235G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984566 | ||||||
chr1:21984590
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0139 | 5 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+259C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984590 | ||||||
chr1:21984622
|
C | A | 2 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.642+291C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984622 | ||||||
chr1:21984634
|
G | T | 2 | a0001c0003t0001g0041a0001c0003t0001g0142 | 3 | NA18950.hp1 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.642+303G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984634 | ||||||
chr1:21984747
|
G | C | 8 | a0000c0018t0002g0173a0000c0019t0002g0174a0004c0008t0001g0027others(5): Show | 9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+416G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984747 | ||||||
chr1:21984816
|
C | T | 5 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(2): Show | 6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+485C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984816 | ||||||
chr1:21984855
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.642+524G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984855 | ||||||
chr1:21984866
|
G | C | 1 | a0001c0011t0001g0024 | 3 | HG01069.hp1 HG01071.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.642+535G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984866 | ||||||
chr1:21984920
|
C | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.642+589C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984920 | ||||||
chr1:21984925
|
C | T | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642+594C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984925 | ||||||
chr1:21984947
|
A | C | 2 | a0001c0003t0001g0013a0001c0003t0001g0068 | 7 | HG02615.hp2 HG02723.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.642+616A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984947 | ||||||
chr1:21984953
|
A | T | 1 | a0002c0002t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.642+622A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984953 | ||||||
chr1:21985016
|
A | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.642+685A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985016 | ||||||
chr1:21985061
|
C | T | 1 | a0001c0003t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.642+730C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985061 | ||||||
chr1:21985063
|
T | C | 5 | a0000c0018t0002g0173a0000c0019t0002g0174a0006c0010t0001g0056others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+732T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985063 | ||||||
chr1:21985130
|
T | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(86): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.642+799T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985130 | ||||||
chr1:21985149
|
G | A | 5 | a0000c0018t0002g0173a0000c0019t0002g0174a0006c0010t0001g0056others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+818G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985149 | ||||||
chr1:21985153
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+822C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985153 | ||||||
chr1:21985163
|
G | T | 23 | a0001c0003t0001g0006a0001c0003t0001g0009a0001c0003t0001g0013others(20): Show | 48 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+832G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985163 | ||||||
chr1:21985183
|
T | C | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+852T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985183 | ||||||
chr1:21985189
|
G | T | 1 | a0001c0001t0001g0055 | 2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.642+858G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985189 | ||||||
chr1:21985274
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.642+943T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985274 | ||||||
chr1:21985275
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0037others(19): Show | 31 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.642+944G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985275 | ||||||
chr1:21985280
|
C | CT | 76 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0007others(73): Show | 135 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.642+964dupT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985280 | |||||
chr1:21985280
|
C | CTT | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.642+963_642+964dup others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985280 | |||||
chr1:21985280
|
CT | C | 7 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(4): Show | 8 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+964delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985280 | |||||
chr1:21985306
|
C | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(42): Show | 60 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.642+975C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985306 | ||||||
chr1:21985319
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+988C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985319 | ||||||
chr1:21985327
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.642+996C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985327 | ||||||
chr1:21985338
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0064others(7): Show | 18 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+1007C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985338 | ||||||
chr1:21985383
|
T | C | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+1052T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985383 | ||||||
chr1:21985389
|
C | A | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+1058C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985389 | ||||||
chr1:21985405
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02818.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.642+1074G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985405 | ||||||
chr1:21985415
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(128): Show | 253 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.642+1084G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985415 | ||||||
chr1:21985477
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(44): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.643-1054C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985477 | ||||||
chr1:21985546
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.643-985G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985546 | ||||||
chr1:21985578
|
A | G | 3 | a0002c0002t0001g0042a0002c0002t0001g0145a0002c0002t0001g0157 | 4 | HG02083.hp2 NA19067.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-953A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985578 | ||||||
chr1:21985595
|
G | GA | 50 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(47): Show | 112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.643-923dupA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985595 | |||||
chr1:21985595
|
GA | G | 5 | a0000c0005t0002g0168a0001c0003t0001g0206a0002c0002t0001g0145others(2): Show | 6 | HG00735.hp2 HG01255.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-923delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985595 | |||||
chr1:21985613
|
C | T | 5 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(2): Show | 6 | HG01243.hp1 HG02004.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-918C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985613 | ||||||
chr1:21985618
|
T | G | 188 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(185): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.643-913T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985618 | ||||||
chr1:21985619
|
T | C | 2 | a0000c0018t0002g0173a0000c0019t0002g0174 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.643-912T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985619 | ||||||
chr1:21985638
|
T | A | 3 | a0000c0018t0002g0173a0000c0019t0002g0174a0013c0025t0001g0078 | 3 | HG01515.hp2 HG01517.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.643-893T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985638 | ||||||
chr1:21985658
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.643-873G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985658 | ||||||
chr1:21985662
|
C | T | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-869C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985662 | ||||||
chr1:21985666
|
C | T | 3 | a0004c0008t0001g0027a0004c0008t0001g0061a0004c0008t0001g0062 | 4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-865C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985666 | ||||||
chr1:21985676
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(7): Show | 27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.643-855G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985676 | ||||||
chr1:21985694
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(45): Show | 110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.643-837A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985694 | ||||||
chr1:21985708
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-823T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985708 | ||||||
chr1:21985726
|
C | G | 1 | a0000c0005t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.643-805C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985726 | ||||||
chr1:21985771
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(45): Show | 110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.643-760G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985771 | ||||||
chr1:21985781
|
C | T | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-750C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985781 | ||||||
chr1:21985783
|
C | T | 3 | a0004c0008t0001g0027a0004c0008t0001g0061a0004c0008t0001g0062 | 4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-748C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985783 | ||||||
chr1:21985794
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-737G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985794 | ||||||
chr1:21985807
|
T | C | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-724T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985807 | ||||||
chr1:21985814
|
C | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(45): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.643-717C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985814 | ||||||
chr1:21985832
|
C | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-699C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985832 | ||||||
chr1:21985848
|
G | A | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.643-683G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985848 | ||||||
chr1:21985851
|
C | A | 7 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(4): Show | 8 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-680C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985851 | ||||||
chr1:21985867
|
G | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-664G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985867 | ||||||
chr1:21985869
|
C | T | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-662C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985869 | ||||||
chr1:21985877
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(44): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.643-654C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985877 | ||||||
chr1:21985892
|
GA | G | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-630delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985892 | |||||
chr1:21985921
|
C | CATT | 193 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(190): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.643-610_643-609ins others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985921 | ||||||
chr1:21985921
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.643-610C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985921 | ||||||
chr1:21985926
|
T | G | 185 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(182): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.643-605T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985926 | ||||||
chr1:21985931
|
T | C | 4 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(1): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-600T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985931 | ||||||
chr1:21985952
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.643-579A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985952 | ||||||
chr1:21985962
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-569T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985962 | ||||||
chr1:21985983
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-548C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985983 | ||||||
chr1:21985984
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.643-547T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985984 | ||||||
chr1:21986009
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.643-522C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986009 | ||||||
chr1:21986100
|
G | A | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-431G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986100 | ||||||
chr1:21986115
|
C | T | 180 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(177): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.643-416C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986115 | ||||||
chr1:21986118
|
A | G | 1 | a0001c0003t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.643-413A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986118 | ||||||
chr1:21986124
|
T | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(44): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.643-407T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986124 | ||||||
chr1:21986174
|
A | G | 179 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(176): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.643-357A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986174 | ||||||
chr1:21986221
|
T | C | 180 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(177): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.643-310T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986221 | ||||||
chr1:21986225
|
T | C | 180 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(177): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.643-306T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986225 | ||||||
chr1:21986242
|
A | G | 1 | a0002c0002t0001g0018 | 5 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-289A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986242 | ||||||
chr1:21986262
|
A | G | 180 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(177): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.643-269A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986262 | ||||||
chr1:21986300
|
C | T | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.643-231C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986300 | ||||||
chr1:21986307
|
C | T | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-224C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986307 | ||||||
chr1:21986308
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.643-223G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986308 | ||||||
chr1:21986330
|
A | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.643-201A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986330 | ||||||
chr1:21986333
|
T | G | 41 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(38): Show | 56 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.643-198T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986333 | ||||||
chr1:21986356
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0195 | 3 | HG01081.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.643-175A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986356 | ||||||
chr1:21986357
|
G | C | 7 | a0000c0005t0002g0046a0000c0005t0002g0167a0000c0005t0002g0168others(4): Show | 9 | HG01081.hp2 HG01243.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-174G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986357 | ||||||
chr1:21986440
|
T | C | 2 | a0006c0010t0001g0175a0006c0010t0001g0176 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.643-91T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986440 | ||||||
chr1:21986505
|
C | T | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.643-26C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986505 | ||||||
chr1:21986512
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-19A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986512 | ||||||
chr1:21986524
|
G | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0177a0001c0001t0001g0178others(26): Show | 60 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(57): Show |
splice_region_variant&intron_variant | LOW | c.643-7G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986524 | ||||||
chr1:21986704
|
C | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(122): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.795+21C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986704 | ||||||
chr1:21986705
|
G | A | 3 | a0004c0008t0001g0027a0004c0008t0001g0061a0004c0008t0001g0062 | 4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+22G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986705 | ||||||
chr1:21986810
|
G | GGGGACGA others(42): Show |
1 | a0002c0006t0001g0152 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.795+132_795+133ins others(49): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21986810 | |||||
chr1:21986867
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.795+184T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986867 | ||||||
chr1:21986878
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(46): Show | 111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.795+195G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986878 | ||||||
chr1:21986976
|
G | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(122): Show | 244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.795+293G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986976 | ||||||
chr1:21987028
|
G | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(45): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.795+345G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987028 | ||||||
chr1:21987051
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG02300.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.795+368C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987051 | ||||||
chr1:21987067
|
A | C | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+384A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987067 | ||||||
chr1:21987068
|
G | A | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+385G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987068 | ||||||
chr1:21987115
|
A | G | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+432A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987115 | ||||||
chr1:21987119
|
C | A | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+436C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987119 | ||||||
chr1:21987122
|
A | G | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+439A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987122 | ||||||
chr1:21987143
|
A | C | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+460A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987143 | ||||||
chr1:21987153
|
G | A | 4 | a0001c0001t0001g0092a0006c0010t0001g0056a0006c0010t0001g0175others(1): Show | 4 | HG00323.hp2 HG01891.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+470G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987153 | ||||||
chr1:21987153
|
GA | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.795+481delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21987153 | |||||
chr1:21987154
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0191 | 3 | HG00323.hp2 HG01255.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.795+471A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987154 | ||||||
chr1:21987155
|
A | G | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.795+472A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987155 | ||||||
chr1:21987163
|
A | G | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+480A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987163 | ||||||
chr1:21987184
|
A | C | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+501A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987184 | ||||||
chr1:21987185
|
G | A | 1 | a0001c0001t0001g0052 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+502G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987185 | ||||||
chr1:21987196
|
A | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.795+513A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987196 | ||||||
chr1:21987237
|
A | G | 2 | a0001c0001t0001g0052a0013c0025t0001g0078 | 3 | HG02004.hp2 HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+554A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987237 | ||||||
chr1:21987242
|
C | T | 2 | a0001c0001t0001g0052a0013c0025t0001g0078 | 3 | HG02004.hp2 HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+559C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987242 | ||||||
chr1:21987332
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.795+649A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987332 | ||||||
chr1:21987365
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.795+682C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987365 | ||||||
chr1:21987427
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.795+744A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987427 | ||||||
chr1:21987462
|
A | T | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+779A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987462 | ||||||
chr1:21987466
|
AAAG | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.795+785_795+787del others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21987466 | |||||
chr1:21987467
|
AAG | A | 21 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0007others(18): Show | 42 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.795+787_795+788del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21987467 | |||||
chr1:21987519
|
T | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0212a0001c0003t0001g0067others(1): Show | 4 | HG01255.hp2 HG03098.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+836T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987519 | ||||||
chr1:21987520
|
G | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0212a0001c0003t0001g0067others(1): Show | 4 | HG01255.hp2 HG03098.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+837G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987520 | ||||||
chr1:21987522
|
GA | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(48): Show | 121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.795+840delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987522 | ||||||
chr1:21987541
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.795+858C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987541 | ||||||
chr1:21987543
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.795+860G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987543 | ||||||
chr1:21987579
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 10 | HG00609.hp1 HG03041.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+896C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987579 | ||||||
chr1:21987585
|
T | A | 20 | a0001c0003t0001g0006a0001c0003t0001g0013a0001c0003t0001g0029others(17): Show | 37 | HG00438.hp1 HG00597.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.795+902T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987585 | ||||||
chr1:21987594
|
A | G | 1 | a0002c0002t0001g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795+911A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987594 | ||||||
chr1:21987609
|
C | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(6): Show | 26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.795+926C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987609 | ||||||
chr1:21987747
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.795+1064A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987747 | ||||||
chr1:21987768
|
G | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0138a0004c0008t0001g0027others(2): Show | 7 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.795+1085G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987768 | ||||||
chr1:21987796
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.795+1113C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987796 | ||||||
chr1:21987797
|
T | C | 43 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(40): Show | 58 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.795+1114T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987797 | ||||||
chr1:21987892
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.795+1209G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987892 | ||||||
chr1:21987906
|
G | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(6): Show | 26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.795+1223G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987906 | ||||||
chr1:21987913
|
T | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(7): Show | 27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.795+1230T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987913 | ||||||
chr1:21987951
|
A | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.795+1268A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987951 | ||||||
chr1:21987977
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(56): Show | 136 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.796-1285G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987977 | ||||||
chr1:21987982
|
G | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.796-1280G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987982 | ||||||
chr1:21987983
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.796-1279T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987983 | ||||||
chr1:21988073
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(44): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.796-1189G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988073 | ||||||
chr1:21988095
|
C | G | 4 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176others(1): Show | 4 | HG01891.hp1 HG02004.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.796-1167C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988095 | ||||||
chr1:21988157
|
C | A | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.796-1105C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988157 | ||||||
chr1:21988157
|
C | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(34): Show | 51 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.796-1105C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988157 | ||||||
chr1:21988235
|
CA | C | 60 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(57): Show | 91 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.796-1020delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988235 | |||||
chr1:21988242
|
AC | A | 6 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(3): Show | 7 | HG02004.hp2 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1019delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988242 | ||||||
chr1:21988297
|
A | AT | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(71): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.796-965_796-964ins others(1): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988297 | ||||||
chr1:21988299
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(47): Show | 120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.796-963T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988299 | ||||||
chr1:21988320
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(49): Show | 122 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.796-942G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988320 | ||||||
chr1:21988341
|
C | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(48): Show | 121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.796-921C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988341 | ||||||
chr1:21988357
|
C | T | 1 | a0013c0025t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.796-905C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988357 | ||||||
chr1:21988480
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.796-782A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988480 | ||||||
chr1:21988507
|
C | T | 4 | a0001c0001t0001g0140a0002c0007t0001g0045a0002c0007t0001g0165others(1): Show | 5 | HG01106.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-755C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988507 | ||||||
chr1:21988520
|
G | A | 2 | a0001c0003t0001g0041a0001c0003t0001g0142 | 3 | NA18950.hp1 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.796-742G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988520 | ||||||
chr1:21988552
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.796-710C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988552 | ||||||
chr1:21988570
|
G | C | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.796-692G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988570 | ||||||
chr1:21988586
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.796-676A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988586 | ||||||
chr1:21988590
|
TA | T | 142 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(139): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.796-652delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988590 | |||||
chr1:21988590
|
TAA | T | 68 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0036others(65): Show | 104 | HG00438.hp1 HG00597.hp2 HG01069.hp2 others(101): Show |
intron_variant | MODIFIER | c.796-653_796-652del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988590 | |||||
chr1:21988614
|
G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(6): Show | 26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.796-648G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988614 | ||||||
chr1:21988745
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.796-517C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988745 | ||||||
chr1:21988762
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.796-500C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988762 | ||||||
chr1:21988825
|
G | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(35): Show | 54 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.796-437G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988825 | ||||||
chr1:21988844
|
T | C | 1 | a0004c0008t0001g0061 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.796-418T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988844 | ||||||
chr1:21988904
|
C | A | 1 | a0012c0023t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.796-358C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988904 | ||||||
chr1:21988905
|
T | C | 215 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(212): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.796-357T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988905 | ||||||
chr1:21988908
|
A | C | 2 | a0002c0006t0001g0152a0012c0023t0001g0214 | 2 | HG02976.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.796-354A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988908 | ||||||
chr1:21988911
|
A | AAT | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.796-344_796-343dup others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988911 | |||||
chr1:21988928
|
TATAC | T | 128 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(125): Show | 247 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.796-314_796-311del others(4): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988928 | |||||
chr1:21988948
|
C | CAT | 2 | a0001c0001t0001g0051a0001c0001t0001g0187 | 3 | HG01258.hp1 HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.796-306_796-305dup others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988948 | |||||
chr1:21988948
|
CAT | C | 3 | a0006c0010t0001g0056a0006c0010t0001g0175a0006c0010t0001g0176 | 3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.796-306_796-305del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988948 | |||||
chr1:21988960
|
C | A | 1 | a0002c0006t0001g0152 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.796-302C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988960 | ||||||
chr1:21988961
|
A | C | 1 | a0002c0006t0001g0152 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.796-301A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988961 | ||||||
chr1:21988966
|
G | T | 175 | a0000c0018t0002g0173a0000c0019t0002g0174a0001c0001t0001g0001others(172): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.796-296G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988966 | ||||||
chr1:21988969
|
G | A | 19 | a0001c0003t0001g0006a0001c0003t0001g0013a0001c0003t0001g0029others(16): Show | 36 | HG00438.hp1 HG00597.hp2 HG02080.hp2 others(33): Show |
intron_variant | MODIFIER | c.796-293G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988969 | ||||||
chr1:21988978
|
TAC | T | 2 | a0002c0002t0001g0018a0009c0017t0001g0170 | 6 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-272_796-271del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988978 | |||||
chr1:21989111
|
C | G | 5 | a0001c0003t0001g0026a0001c0003t0001g0057a0001c0003t0001g0058others(2): Show | 6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-151C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989111 | ||||||
chr1:21989153
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.796-109T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989153 | ||||||
chr1:21989169
|
C | T | 2 | a0000c0019t0002g0174a0004c0008t0001g0061 | 2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.796-93C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989169 | ||||||
chr1:21989191
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(6): Show | 26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.796-71C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989191 | ||||||
chr1:21989217
|
G | A | 2 | a0000c0019t0002g0174a0004c0008t0001g0061 | 2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.796-45G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989217 | ||||||
chr1:21989222
|
C | T | 4 | a0001c0001t0001g0140a0002c0007t0001g0045a0002c0007t0001g0165others(1): Show | 5 | HG01106.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-40C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989222 | ||||||
chr1:21989245
|
C | T | 99 | a0000c0019t0002g0174a0001c0001t0001g0001a0001c0001t0001g0003others(96): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.796-17C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989245 | ||||||
chr1:21989249
|
C | A | 2 | a0001c0003t0001g0026a0001c0003t0001g0057 | 3 | HG02895.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.796-13C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989249 |