geneid | 794 |
---|---|
ensemblid | ENSG00000172137.19 |
hgncid | 1435 |
symbol | CALB2 |
name | calbindin 2 |
refseq_nuc | NM_001740.5 |
refseq_prot | NP_001731.2 |
ensembl_nuc | ENST00000302628.9 |
ensembl_prot | ENSP00000307508.4 |
mane_status | MANE Select |
chr | chr16 |
start | 71358723 |
end | 71390433 |
strand | + |
ver | v1.2 |
region | chr16:71358723-71390433 |
region5000 | chr16:71353723-71395433 |
regionname0 | CALB2_chr16_71358723_71390433 |
regionname5000 | CALB2_chr16_71353723_71395433 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 271 | 383 | 79 | 65 | 185 | 12 | 40 | 145 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0002 | 0/0 | 271 | 42 | 15 | 11 | 8 | 2 | 6 | 6 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0003 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 816 | 380 | 78 | 65 | 183 | 12 | 40 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
c0002 | 0/0 | 816 | 42 | 15 | 11 | 8 | 2 | 6 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
c0003 | 0/0 | 816 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
c0004 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
c0005 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 639 | 277 | 64 | 59 | 114 | 8 | 31 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
t0002 | 1/0 | 639 | 130 | 13 | 17 | 79 | 6 | 14 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
t0003 | 0/0 | 638 | 16 | 16 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
t0004 | 0/0 | 639 | 3 | 1 | 0 | 1 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0008 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0020 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 816 | 380 | 78 | 65 | 183 | 12 | 40 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0001c0003 | 0/0 | 816 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0001c0004 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0002c0002 | 0/0 | 816 | 42 | 15 | 11 | 8 | 2 | 6 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0003c0005 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1454 | 267 | 60 | 57 | 112 | 8 | 29 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0001c0001t0002 | 1/0 | 1454 | 97 | 2 | 8 | 71 | 4 | 11 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0001c0001t0003 | 0/0 | 1453 | 16 | 16 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0001c0003t0001 | 0/0 | 1454 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0001c0004t0001 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0002c0002t0001 | 0/0 | 1454 | 7 | 3 | 2 | 0 | 0 | 2 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0002c0002t0002 | 0/0 | 1454 | 32 | 11 | 9 | 7 | 2 | 3 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0002c0002t0004 | 0/0 | 1454 | 3 | 1 | 0 | 1 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
a0003c0005t0002 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | copy fasta | chr16 | 71353723 | 71395433 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0020 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0001c0004t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0002c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
a0003c0005t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0346 | EUR | GBR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0246 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0244 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0289 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0279 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02165 | hp2 | a0002 | c0002 | t0004 | g0266 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0348 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02622 | hp1 | a0002 | c0002 | t0004 | g0047 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0256 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0356 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0347 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0239 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0253 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0162 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03669 | hp2 | a0002 | c0002 | t0004 | g0265 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0344 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0158 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19066 | hp2 | a0003 | c0005 | t0002 | g0005 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | ASW | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0254 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | GIH | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | GIH | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0020 | REF | REF | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0329 | REF | REF | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71377733
|
G | A | 1 | a0002 | 42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
missense_variant | MODERATE | c.328G>A | p.Ala110Thr | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/11 | 398/1454 | 328/816 | 110/271 | chr16 | 71377733 | ||
chr16:71389825
|
A | G | 1 | a0003 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.776A>G | p.Lys259Arg | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 846/1454 | 776/816 | 259/271 | chr16 | 71389825 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71382754
|
C | T | 1 | a0001c0003 | 2 | NA18974.hp1 NA18982.hp2 |
synonymous_variant | LOW | c.378C>T | p.Tyr126Tyr | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/11 | 448/1454 | 378/816 | 126/271 | chr16 | 71382754 | ||
chr16:71383411
|
T | C | 1 | a0001c0004 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.444T>C | p.Asp148Asp | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/11 | 514/1454 | 444/816 | 148/271 | chr16 | 71383411 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71390003
|
T | C | 6 | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(3): Show | 296 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*138T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 138 | chr16 | 71390003 | |||||
chr16:71390025
|
TG | T | 1 | a0001c0001t0003 | 16 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*166delG | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 166 | INFO_REALIGN_3_PRIME | chr16 | 71390025 | ||||
chr16:71390137
|
C | T | 1 | a0002c0002t0004 | 3 | HG02165.hp2 HG02622.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*272C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 272 | chr16 | 71390137 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:71359202
|
C | G | 1 | a0001c0001t0001g0372 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.94+316C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359202 | ||||||
chr16:71359409
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+523C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359409 | ||||||
chr16:71359488
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0003g0035 | 3 | HG01515.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.94+602G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359488 | ||||||
chr16:71359633
|
A | G | 1 | a0001c0001t0001g0371 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.94+747A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359633 | ||||||
chr16:71359660
|
A | G | 1 | a0001c0001t0001g0370 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.94+774A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359660 | ||||||
chr16:71359787
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.94+901G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359787 | ||||||
chr16:71359840
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 5 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+954G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359840 | ||||||
chr16:71360310
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94+1424G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360310 | ||||||
chr16:71360391
|
A | T | 1 | a0001c0001t0002g0369 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.94+1505A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360391 | ||||||
chr16:71360537
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94+1651C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360537 | ||||||
chr16:71360692
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0365others(3): Show | 9 | HG02630.hp1 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1806A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360692 | ||||||
chr16:71360838
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+1952G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360838 | ||||||
chr16:71360849
|
T | G | 10 | a0001c0001t0001g0037a0002c0002t0002g0012a0002c0002t0002g0044others(7): Show | 11 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+1963T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360849 | ||||||
chr16:71360956
|
C | T | 1 | a0002c0002t0002g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.94+2070C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360956 | ||||||
chr16:71361010
|
C | T | 1 | a0001c0001t0001g0364 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.94+2124C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361010 | ||||||
chr16:71361011
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.94+2125G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361011 | ||||||
chr16:71361043
|
A | G | 1 | a0001c0001t0001g0363 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.94+2157A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361043 | ||||||
chr16:71361229
|
C | T | 5 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(2): Show | 5 | HG01943.hp1 HG01981.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+2343C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361229 | ||||||
chr16:71361253
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.94+2367G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361253 | ||||||
chr16:71361322
|
C | G | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+2436C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361322 | ||||||
chr16:71361483
|
C | T | 6 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0048others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+2597C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361483 | ||||||
chr16:71361602
|
A | G | 1 | a0001c0001t0002g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.94+2716A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361602 | ||||||
chr16:71361634
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.94+2748T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361634 | ||||||
chr16:71361695
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.94+2809G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361695 | ||||||
chr16:71361901
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(122): Show | 138 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.94+3015G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361901 | ||||||
chr16:71361992
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.94+3106T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361992 | ||||||
chr16:71362156
|
A | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.94+3270A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362156 | ||||||
chr16:71362163
|
C | A | 1 | a0002c0002t0002g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+3277C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362163 | ||||||
chr16:71362183
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.94+3297C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362183 | ||||||
chr16:71362232
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.94+3346A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362232 | ||||||
chr16:71362251
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0002g0273 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94+3365C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362251 | ||||||
chr16:71362269
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 162 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.94+3383A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362269 | ||||||
chr16:71362370
|
C | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+3484C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362370 | ||||||
chr16:71362387
|
A | G | 31 | a0001c0001t0001g0037a0001c0001t0001g0250a0001c0001t0001g0257others(28): Show | 37 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.94+3501A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362387 | ||||||
chr16:71362454
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+3568G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362454 | ||||||
chr16:71362505
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+3619G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362505 | ||||||
chr16:71362581
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+3695C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362581 | ||||||
chr16:71362758
|
G | A | 17 | a0001c0001t0001g0250a0002c0002t0001g0249a0002c0002t0001g0251others(14): Show | 22 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+3872G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362758 | ||||||
chr16:71362759
|
G | GCT | 93 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(90): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+3880_94+3881dup others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71362759 | |||||
chr16:71362774
|
T | G | 13 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 18 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+3888T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362774 | ||||||
chr16:71362943
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18997.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.94+4057G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362943 | ||||||
chr16:71362998
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(124): Show | 140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.94+4112A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362998 | ||||||
chr16:71363005
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0152others(2): Show | 7 | HG01884.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4119C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363005 | ||||||
chr16:71363011
|
C | A | 3 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+4125C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363011 | ||||||
chr16:71363018
|
T | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(279): Show | 313 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.94+4132T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363018 | ||||||
chr16:71363057
|
G | A | 3 | a0002c0002t0002g0245a0002c0002t0002g0246a0002c0002t0002g0247 | 3 | HG00280.hp1 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.94+4171G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363057 | ||||||
chr16:71363200
|
C | A | 1 | a0001c0001t0001g0364 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.94+4314C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363200 | ||||||
chr16:71363342
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0163a0002c0002t0002g0162 | 3 | HG03239.hp2 NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.94+4456T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363342 | ||||||
chr16:71363440
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.94+4554G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363440 | ||||||
chr16:71363575
|
C | T | 1 | a0002c0002t0002g0256 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.94+4689C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363575 | ||||||
chr16:71363580
|
C | T | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+4694C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363580 | ||||||
chr16:71363616
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.94+4730G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363616 | ||||||
chr16:71363694
|
G | C | 8 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | HG00738.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+4808G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363694 | ||||||
chr16:71363757
|
A | G | 5 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(2): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+4871A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363757 | ||||||
chr16:71363859
|
CTGGGAAC others(6): Show |
C | 1 | a0001c0001t0002g0283 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+4975_94+4987del others(13): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71363859 | |||||
chr16:71363968
|
G | A | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+5082G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363968 | ||||||
chr16:71363974
|
C | T | 17 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0003g0030others(14): Show | 18 | HG01891.hp2 HG02109.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+5088C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363974 | ||||||
chr16:71364028
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00597.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.94+5142C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364028 | ||||||
chr16:71364057
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(119): Show | 135 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.94+5171C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364057 | ||||||
chr16:71364220
|
T | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 88 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+5334T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364220 | ||||||
chr16:71364281
|
T | A | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5395T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364281 | ||||||
chr16:71364282
|
T | G | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5396T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364282 | ||||||
chr16:71364284
|
A | G | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5398A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364284 | ||||||
chr16:71364285
|
T | C | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5399T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364285 | ||||||
chr16:71364287
|
T | G | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5401T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364287 | ||||||
chr16:71364288
|
T | C | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5402T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364288 | ||||||
chr16:71364289
|
G | T | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5403G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364289 | ||||||
chr16:71364290
|
A | ACCAGCC | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5405_94+5406ins others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71364290 | |||||
chr16:71364300
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0118others(1): Show | 5 | HG00544.hp1 NA18947.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+5414C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364300 | ||||||
chr16:71364307
|
C | A | 2 | a0001c0001t0001g0274a0001c0001t0002g0273 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94+5421C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364307 | ||||||
chr16:71364492
|
C | T | 1 | a0001c0001t0002g0351 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.94+5606C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364492 | ||||||
chr16:71365044
|
C | T | 1 | a0002c0002t0002g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+6158C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365044 | ||||||
chr16:71365289
|
G | A | 93 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(90): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+6403G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365289 | ||||||
chr16:71365297
|
C | T | 1 | a0001c0001t0002g0350 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.94+6411C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365297 | ||||||
chr16:71365322
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.94+6436G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365322 | ||||||
chr16:71365366
|
G | A | 3 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029 | 6 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+6480G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365366 | ||||||
chr16:71365394
|
C | G | 101 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0023others(98): Show | 107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.94+6508C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365394 | ||||||
chr16:71365676
|
A | T | 93 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(90): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-6477A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365676 | ||||||
chr16:71365718
|
C | G | 1 | a0002c0002t0002g0255 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.95-6435C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365718 | ||||||
chr16:71365728
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-6425T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365728 | ||||||
chr16:71365814
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0003g0054others(1): Show | 4 | HG02922.hp2 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6339G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365814 | ||||||
chr16:71365947
|
G | A | 2 | a0002c0002t0002g0248a0002c0002t0002g0255 | 2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.95-6206G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365947 | ||||||
chr16:71365980
|
G | A | 27 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(24): Show | 29 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.95-6173G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365980 | ||||||
chr16:71366006
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-6147T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366006 | ||||||
chr16:71366020
|
CTCTCT | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-6131_95-6127del others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366020 | |||||
chr16:71366022
|
C | CTTTTT | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0274others(1): Show | 4 | HG02071.hp1 HG02165.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(2): Show |
34 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0159others(31): Show | 35 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(9): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(3): Show |
37 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0160others(34): Show | 38 | HG00280.hp2 HG01123.hp2 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(4): Show |
15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0180others(12): Show | 17 | HG00423.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(11): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0355 | 3 | HG03688.hp2 NA18949.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(13): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(14): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0070 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0071 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(19): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(13): Show |
15 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0036others(12): Show | 17 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(14): Show |
51 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(48): Show | 60 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(15): Show |
23 | a0001c0001t0001g0043a0001c0001t0001g0097a0001c0001t0001g0098others(20): Show | 23 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(22): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG01070.hp1 HG01168.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(23): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(24): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02155.hp2 HG03688.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(25): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0116 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(27): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366022
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(28): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | |||||
chr16:71366024
|
C | CT | 5 | a0001c0001t0002g0032a0001c0001t0002g0346a0001c0001t0002g0349others(2): Show | 6 | HG00140.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6109dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTT | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-6113_95-6109dup others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(7): Show |
4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6122_95-6109dup others(14): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0280a0001c0001t0001g0281a0002c0002t0002g0279 | 3 | HG00738.hp2 HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.95-6123_95-6109dup others(15): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-6124_95-6109dup others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(14): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0120a0001c0001t0001g0152others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0022a0001c0001t0003g0267 | 3 | HG02896.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(22): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0270 | 3 | HG02258.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(23): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0003g0030a0001c0001t0003g0271a0002c0002t0001g0258 | 4 | HG02818.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(24): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0003g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-6109_95-6108ins others(25): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | HG01943.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(27): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0360a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG02293.hp2 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(28): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0361 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.95-6109_95-6108ins others(29): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0362 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.95-6109_95-6108ins others(33): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366024
|
C | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(202): Show | 220 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.95-6129C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366024 | ||||||
chr16:71366024
|
CT | C | 6 | a0001c0001t0002g0055a0001c0001t0002g0242a0001c0001t0002g0284others(3): Show | 6 | HG00673.hp1 HG01069.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6109delT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | |||||
chr16:71366025
|
T | TC | 25 | a0001c0001t0001g0250a0002c0002t0001g0251a0002c0002t0001g0252others(22): Show | 31 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.95-6128_95-6127ins others(1): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366025 | ||||||
chr16:71366026
|
T | C | 1 | a0002c0002t0002g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-6127T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366026 | ||||||
chr16:71366027
|
T | C | 1 | a0002c0002t0001g0249 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.95-6126T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366027 | ||||||
chr16:71366127
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-6026C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366127 | ||||||
chr16:71366188
|
G | A | 1 | a0002c0002t0004g0266 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.95-5965G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366188 | ||||||
chr16:71366217
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.95-5936G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366217 | ||||||
chr16:71366228
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(176): Show | 204 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.95-5925G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366228 | ||||||
chr16:71366324
|
C | CT | 24 | a0001c0001t0001g0213a0001c0001t0001g0250a0001c0001t0001g0337others(21): Show | 26 | HG00280.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-5809dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366324 | |||||
chr16:71366324
|
C | CTT | 6 | a0002c0002t0002g0006a0002c0002t0002g0029a0002c0002t0002g0244others(3): Show | 9 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-5810_95-5809dup others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366324 | |||||
chr16:71366338
|
T | G | 6 | a0001c0001t0002g0031a0001c0001t0002g0284a0001c0001t0002g0287others(3): Show | 7 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-5815T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366338 | ||||||
chr16:71366344
|
TG | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(212): Show | 233 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.95-5808delG | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366344 | ||||||
chr16:71366344
|
TGA | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 27 | HG01109.hp1 HG01256.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.95-5797_95-5796del others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366344 | |||||
chr16:71366345
|
G | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0066others(39): Show | 48 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-5808G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366345 | ||||||
chr16:71366346
|
A | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(254): Show | 281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.95-5807A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366346 | ||||||
chr16:71366532
|
T | C | 2 | a0002c0002t0002g0248a0002c0002t0002g0255 | 2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.95-5621T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366532 | ||||||
chr16:71366630
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-5523T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366630 | ||||||
chr16:71366676
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95-5477G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366676 | ||||||
chr16:71366830
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.95-5323G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366830 | ||||||
chr16:71366858
|
G | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.95-5295G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366858 | ||||||
chr16:71367055
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0002g0273 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-5098G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367055 | ||||||
chr16:71367117
|
G | T | 5 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(2): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-5036G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367117 | ||||||
chr16:71367124
|
C | T | 19 | a0001c0001t0001g0250a0002c0002t0001g0249a0002c0002t0001g0251others(16): Show | 24 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-5029C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367124 | ||||||
chr16:71367139
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0178 | 2 | HG01517.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.95-5014G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367139 | ||||||
chr16:71367165
|
G | A | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-4988G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367165 | ||||||
chr16:71367168
|
A | G | 8 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | HG00738.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-4985A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367168 | ||||||
chr16:71367274
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0081 | 2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.95-4879G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367274 | ||||||
chr16:71367291
|
CGTCTTTA others(5): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.95-4848_95-4837del others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71367291 | |||||
chr16:71367434
|
C | A | 1 | a0001c0001t0002g0283 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.95-4719C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367434 | ||||||
chr16:71367565
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.95-4588C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367565 | ||||||
chr16:71367602
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0003g0054others(1): Show | 4 | HG02922.hp2 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4551C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367602 | ||||||
chr16:71367651
|
T | C | 56 | a0001c0001t0001g0232a0001c0001t0001g0241a0001c0001t0001g0291others(53): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.95-4502T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367651 | ||||||
chr16:71367752
|
T | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(51): Show | 63 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.95-4401T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367752 | ||||||
chr16:71367821
|
G | A | 5 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(2): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-4332G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367821 | ||||||
chr16:71367890
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(9): Show | 14 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-4263G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367890 | ||||||
chr16:71368038
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.95-4115G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368038 | ||||||
chr16:71368161
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0038others(3): Show | 8 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-3992C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368161 | ||||||
chr16:71368423
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.95-3730G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368423 | ||||||
chr16:71368439
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0002g0273 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-3714A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368439 | ||||||
chr16:71368506
|
A | AAAAATAA others(3): Show |
10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-3637_95-3628dup others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71368506 | |||||
chr16:71368612
|
G | A | 1 | a0002c0002t0002g0012 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.95-3541G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368612 | ||||||
chr16:71368642
|
G | A | 20 | a0001c0001t0001g0250a0002c0002t0001g0249a0002c0002t0001g0251others(17): Show | 25 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.95-3511G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368642 | ||||||
chr16:71368704
|
T | C | 47 | a0001c0001t0001g0250a0001c0001t0001g0262a0001c0001t0001g0263others(44): Show | 54 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.95-3449T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368704 | ||||||
chr16:71368718
|
G | A | 1 | a0001c0001t0001g0362 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.95-3435G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368718 | ||||||
chr16:71368750
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-3403G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368750 | ||||||
chr16:71368851
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0002g0273 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-3302C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368851 | ||||||
chr16:71368861
|
G | A | 1 | a0001c0001t0001g0355 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.95-3292G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368861 | ||||||
chr16:71369025
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.95-3128C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369025 | ||||||
chr16:71369038
|
G | A | 8 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0267others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-3115G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369038 | ||||||
chr16:71369096
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.95-3057A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369096 | ||||||
chr16:71369180
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(119): Show | 135 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.95-2973C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369180 | ||||||
chr16:71369194
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.95-2959G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369194 | ||||||
chr16:71369332
|
C | T | 49 | a0001c0001t0001g0250a0001c0001t0001g0262a0001c0001t0001g0263others(46): Show | 56 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.95-2821C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369332 | ||||||
chr16:71369399
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-2754C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369399 | ||||||
chr16:71369422
|
G | A | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0209others(3): Show | 6 | NA18941.hp2 NA18946.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-2731G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369422 | ||||||
chr16:71369561
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0002g0356 | 2 | HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.95-2592T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369561 | ||||||
chr16:71369682
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.95-2471C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369682 | ||||||
chr16:71369756
|
C | A | 1 | a0001c0001t0001g0352 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.95-2397C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369756 | ||||||
chr16:71369777
|
C | CTGA | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-2376_95-2375ins others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369777 | ||||||
chr16:71369778
|
C | CGAG | 274 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(271): Show | 304 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.95-2374_95-2372dup others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71369778 | |||||
chr16:71369778
|
C | G | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-2375C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369778 | ||||||
chr16:71369915
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.95-2238C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369915 | ||||||
chr16:71369931
|
A | C | 1 | a0001c0001t0002g0321 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.95-2222A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369931 | ||||||
chr16:71369972
|
G | A | 8 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0267others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-2181G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369972 | ||||||
chr16:71370106
|
A | G | 8 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0267others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-2047A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370106 | ||||||
chr16:71370267
|
C | A | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0292 | 3 | NA18977.hp1 NA18994.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.95-1886C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370267 | ||||||
chr16:71370482
|
TA | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 19 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-1658delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71370482 | |||||
chr16:71370484
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-1669A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370484 | ||||||
chr16:71370605
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.95-1548C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370605 | ||||||
chr16:71370786
|
C | T | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-1367C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370786 | ||||||
chr16:71370877
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(128): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.95-1276C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370877 | ||||||
chr16:71370901
|
G | A | 4 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(1): Show | 4 | HG01981.hp2 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1252G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370901 | ||||||
chr16:71370940
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-1213T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370940 | ||||||
chr16:71370969
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(115): Show | 131 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.95-1184G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370969 | ||||||
chr16:71371015
|
C | A | 2 | a0001c0001t0001g0238a0001c0004t0001g0239 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.95-1138C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371015 | ||||||
chr16:71371086
|
G | T | 8 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0267others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1067G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371086 | ||||||
chr16:71371095
|
C | T | 281 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(278): Show | 312 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.95-1058C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371095 | ||||||
chr16:71371141
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.95-1012G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371141 | ||||||
chr16:71371691
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-462C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371691 | ||||||
chr16:71371737
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.95-416G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371737 | ||||||
chr16:71371816
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-337G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371816 | ||||||
chr16:71371881
|
C | T | 88 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(85): Show | 92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-272C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371881 | ||||||
chr16:71371917
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.95-236G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371917 | ||||||
chr16:71372121
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 151 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.95-32C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71372121 | ||||||
chr16:71372244
|
G | A | 1 | a0002c0002t0002g0254 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.171+15G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372244 | ||||||
chr16:71372249
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.171+20C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372249 | ||||||
chr16:71372285
|
C | T | 5 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(2): Show | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+56C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372285 | ||||||
chr16:71372346
|
A | T | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0023others(105): Show | 115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.171+117A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372346 | ||||||
chr16:71372384
|
G | A | 42 | a0001c0001t0001g0250a0001c0001t0001g0262a0001c0001t0001g0263others(39): Show | 48 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.171+155G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372384 | ||||||
chr16:71372425
|
G | A | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(3): Show | 6 | HG02809.hp1 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+196G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372425 | ||||||
chr16:71372458
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.171+229T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372458 | ||||||
chr16:71372478
|
G | A | 3 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171+249G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372478 | ||||||
chr16:71372488
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.171+259C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372488 | ||||||
chr16:71372640
|
G | A | 31 | a0001c0001t0001g0250a0002c0002t0001g0249a0002c0002t0001g0251others(28): Show | 37 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.171+411G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372640 | ||||||
chr16:71372700
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 151 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.171+471C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372700 | ||||||
chr16:71372743
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.171+514C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372743 | ||||||
chr16:71372855
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.171+626C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372855 | ||||||
chr16:71372876
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+647G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372876 | ||||||
chr16:71373090
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.171+861T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373090 | ||||||
chr16:71373120
|
CTG | C | 5 | a0001c0001t0002g0283a0001c0001t0002g0322a0001c0001t0002g0323others(2): Show | 5 | HG02135.hp2 NA19000.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+894_171+895del others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 71373120 | |||||
chr16:71373214
|
C | G | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.171+985C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373214 | ||||||
chr16:71373239
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.171+1010C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373239 | ||||||
chr16:71373295
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(129): Show | 150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.171+1066G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373295 | ||||||
chr16:71373408
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.171+1179T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373408 | ||||||
chr16:71373472
|
G | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1243G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373472 | ||||||
chr16:71373479
|
C | T | 9 | a0002c0002t0002g0012a0002c0002t0002g0044a0002c0002t0002g0045others(6): Show | 10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+1250C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373479 | ||||||
chr16:71373622
|
T | C | 42 | a0001c0001t0001g0250a0001c0001t0001g0262a0001c0001t0001g0263others(39): Show | 48 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.172-1123T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373622 | ||||||
chr16:71373627
|
A | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 267 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.172-1118A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373627 | ||||||
chr16:71373824
|
C | A | 8 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0267others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-921C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373824 | ||||||
chr16:71374092
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.172-653G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374092 | ||||||
chr16:71374147
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0003g0035 | 3 | HG01515.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.172-598G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374147 | ||||||
chr16:71374214
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-531G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374214 | ||||||
chr16:71374384
|
G | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.172-361G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374384 | ||||||
chr16:71374462
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.172-283G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374462 | ||||||
chr16:71374572
|
T | G | 96 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(93): Show | 101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.172-173T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374572 | ||||||
chr16:71374573
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.172-172T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374573 | ||||||
chr16:71374613
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.172-132A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374613 | ||||||
chr16:71374624
|
A | G | 103 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(100): Show | 108 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.172-121A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374624 | ||||||
chr16:71375037
|
G | A | 150 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0023others(147): Show | 163 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.261+203G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375037 | ||||||
chr16:71375066
|
C | A | 1 | a0001c0001t0002g0192 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.261+232C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375066 | ||||||
chr16:71375214
|
C | T | 36 | a0002c0002t0001g0207a0002c0002t0001g0249a0002c0002t0001g0251others(33): Show | 42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.261+380C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375214 | ||||||
chr16:71375235
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.261+401C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375235 | ||||||
chr16:71375240
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.261+406G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375240 | ||||||
chr16:71375252
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.261+418T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375252 | ||||||
chr16:71375306
|
A | G | 6 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0048others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+472A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375306 | ||||||
chr16:71375324
|
G | A | 9 | a0001c0001t0001g0298a0001c0001t0001g0337a0001c0001t0002g0055others(6): Show | 9 | NA18940.hp1 NA18942.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+490G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375324 | ||||||
chr16:71375428
|
G | A | 1 | a0001c0001t0003g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.261+594G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375428 | ||||||
chr16:71375434
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(5): Show | 10 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.261+600C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375434 | ||||||
chr16:71375442
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.261+608A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375442 | ||||||
chr16:71375475
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.261+641G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375475 | ||||||
chr16:71375476
|
C | T | 36 | a0002c0002t0001g0207a0002c0002t0001g0249a0002c0002t0001g0251others(33): Show | 42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.261+642C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375476 | ||||||
chr16:71375575
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261+741G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375575 | ||||||
chr16:71375739
|
G | A | 3 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.261+905G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375739 | ||||||
chr16:71375893
|
G | A | 2 | a0002c0002t0002g0158a0002c0002t0002g0279 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+1059G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375893 | ||||||
chr16:71376154
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.261+1320G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376154 | ||||||
chr16:71376217
|
G | T | 84 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(81): Show | 88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.261+1383G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376217 | ||||||
chr16:71376338
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.262-1329G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376338 | ||||||
chr16:71376348
|
G | C | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.262-1319G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376348 | ||||||
chr16:71376455
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-1212G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376455 | ||||||
chr16:71376507
|
A | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 5 | NA18965.hp2 NA18966.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-1160A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376507 | ||||||
chr16:71376535
|
G | GCATCCAC others(183): Show |
7 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG00738.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-1106_262-917du others(191): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 71376535 | |||||
chr16:71376616
|
C | A | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.262-1051C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376616 | ||||||
chr16:71376659
|
C | A | 36 | a0002c0002t0001g0207a0002c0002t0001g0249a0002c0002t0001g0251others(33): Show | 42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.262-1008C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376659 | ||||||
chr16:71376714
|
TACA | T | 5 | a0001c0001t0002g0031a0001c0001t0002g0284a0001c0001t0002g0288others(2): Show | 6 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-950_262-948del others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 71376714 | |||||
chr16:71376738
|
A | G | 7 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG01981.hp2 HG01993.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-929A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376738 | ||||||
chr16:71376765
|
A | G | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(3): Show | 6 | HG02809.hp1 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-902A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376765 | ||||||
chr16:71376770
|
TACATGCA others(3): Show |
T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-889_262-880del others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 71376770 | |||||
chr16:71377094
|
G | A | 84 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(81): Show | 88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.262-573G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71377094 | ||||||
chr16:71377343
|
A | G | 1 | a0001c0001t0001g0368 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.262-324A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71377343 | ||||||
chr16:71377543
|
G | T | 276 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(273): Show | 307 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.262-124G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71377543 | ||||||
chr16:71377896
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.342+149G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71377896 | ||||||
chr16:71377897
|
G | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(128): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.342+150G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71377897 | ||||||
chr16:71378117
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.342+370G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378117 | ||||||
chr16:71378383
|
TA | T | 24 | a0001c0001t0001g0061a0001c0001t0001g0067a0001c0001t0001g0077others(21): Show | 24 | HG01168.hp1 HG01168.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+651delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71378383 | |||||
chr16:71378473
|
C | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.342+726C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378473 | ||||||
chr16:71378480
|
T | C | 102 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(99): Show | 107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.342+733T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378480 | ||||||
chr16:71378665
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.342+918T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378665 | ||||||
chr16:71378739
|
G | A | 1 | a0001c0001t0003g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.342+992G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378739 | ||||||
chr16:71378779
|
C | T | 38 | a0001c0001t0001g0357a0001c0001t0002g0296a0001c0001t0002g0297others(35): Show | 44 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.342+1032C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378779 | ||||||
chr16:71378825
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342+1078T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378825 | ||||||
chr16:71378882
|
G | A | 1 | a0001c0001t0001g0370 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.342+1135G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378882 | ||||||
chr16:71378928
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.342+1181G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378928 | ||||||
chr16:71378985
|
T | C | 111 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(108): Show | 116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.342+1238T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378985 | ||||||
chr16:71379033
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.342+1286T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379033 | ||||||
chr16:71379074
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 318 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.342+1327T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379074 | ||||||
chr16:71379232
|
G | A | 2 | a0002c0002t0002g0158a0002c0002t0002g0279 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.342+1485G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379232 | ||||||
chr16:71379271
|
T | TAATA | 14 | a0001c0001t0001g0042a0001c0001t0001g0118a0001c0001t0001g0121others(11): Show | 15 | HG00544.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+1567_342+1570d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | |||||
chr16:71379271
|
TAATA | T | 90 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0072others(87): Show | 111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.342+1567_342+1570d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | |||||
chr16:71379271
|
TAATAAAT others(1): Show |
T | 99 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0023others(96): Show | 105 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.342+1563_342+1570d others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | |||||
chr16:71379271
|
TAATAAAT others(5): Show |
T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18961.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.342+1559_342+1570d others(14): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | |||||
chr16:71379402
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.342+1655T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379402 | ||||||
chr16:71379416
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.342+1669T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379416 | ||||||
chr16:71379580
|
C | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 134 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.342+1833C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379580 | ||||||
chr16:71379649
|
C | T | 6 | a0001c0001t0002g0285a0001c0001t0002g0326a0001c0001t0002g0333others(3): Show | 6 | NA18943.hp2 NA18952.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+1902C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379649 | ||||||
chr16:71379771
|
T | A | 3 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.342+2024T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379771 | ||||||
chr16:71379782
|
GCAGA | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0122others(5): Show | 9 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+2039_342+2042d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379782 | |||||
chr16:71379789
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342+2042G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379789 | ||||||
chr16:71379818
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.342+2071G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379818 | ||||||
chr16:71379939
|
G | GACATTCT others(56): Show |
1 | a0001c0001t0001g0122 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.342+2193_342+2255d others(65): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379939 | |||||
chr16:71380148
|
C | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 15 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.342+2401C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380148 | ||||||
chr16:71380148
|
C | G | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.342+2401C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380148 | ||||||
chr16:71380156
|
G | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(131): Show | 152 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.342+2409G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380156 | ||||||
chr16:71380160
|
G | C | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.342+2413G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380160 | ||||||
chr16:71380205
|
T | A | 12 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0054others(9): Show | 13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.342+2458T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380205 | ||||||
chr16:71380221
|
T | A | 1 | a0001c0001t0002g0302 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.342+2474T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380221 | ||||||
chr16:71380254
|
ATTTCTTT others(2): Show |
A | 9 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0280others(6): Show | 10 | HG00735.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-2453_343-2445d others(11): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380254 | |||||
chr16:71380268
|
T | A | 1 | a0002c0002t0002g0279 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-2451T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380268 | ||||||
chr16:71380287
|
C | CT | 6 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0123others(3): Show | 7 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-2428dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380287
|
CTTTTCTT others(3): Show |
C | 5 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0365others(2): Show | 8 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-2427_343-2418d others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380287
|
CTTTTCTT others(4): Show |
C | 6 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0042others(3): Show | 8 | HG01109.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-2427_343-2417d others(13): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380287
|
CTTTTCTT others(6): Show |
C | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.343-2427_343-2415d others(15): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380287
|
CTTTTCTT others(7): Show |
C | 14 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0064others(11): Show | 16 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-2427_343-2414d others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380287
|
CTTTTCTT others(11): Show |
C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(3): Show | 8 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-2427_343-2410d others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380287
|
CTTTTCTT others(12): Show |
C | 1 | a0001c0001t0003g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-2427_343-2409d others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | |||||
chr16:71380288
|
TTTTC | T | 31 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0061others(28): Show | 32 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.343-2427_343-2424d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380288 | |||||
chr16:71380289
|
TTTC | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(35): Show | 44 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.343-2427_343-2425d others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380289 | |||||
chr16:71380290
|
TTC | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0083others(12): Show | 16 | HG01123.hp1 HG01433.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-2427_343-2426d others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380290 | |||||
chr16:71380291
|
TC | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0065others(5): Show | 9 | HG01884.hp2 HG02165.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-2427delC | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380291 | ||||||
chr16:71380292
|
C | CT | 16 | a0001c0001t0001g0263a0001c0001t0001g0291a0001c0001t0002g0005others(13): Show | 18 | HG01192.hp1 HG01358.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.343-2392dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
C | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0080others(7): Show | 11 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.343-2427C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380292 | ||||||
chr16:71380292
|
CT | C | 31 | a0001c0001t0001g0205a0001c0001t0001g0232a0001c0001t0001g0277others(28): Show | 37 | HG00438.hp1 HG00544.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.343-2392delT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTT | C | 34 | a0001c0001t0001g0159a0001c0001t0001g0176a0001c0001t0001g0186others(31): Show | 43 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.343-2393_343-2392d others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTT | C | 37 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0040others(34): Show | 40 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.343-2394_343-2392d others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTT | C | 37 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0139others(34): Show | 38 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.343-2395_343-2392d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTTT | C | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0194others(3): Show | 6 | HG01517.hp1 HG02015.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-2396_343-2392d others(7): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0341 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.343-2404_343-2392d others(15): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.343-2407_343-2392d others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTTTTT others(10): Show |
C | 3 | a0002c0002t0002g0048a0002c0002t0002g0245a0002c0002t0002g0247 | 3 | HG01255.hp2 HG02055.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.343-2408_343-2392d others(19): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTTTTT others(11): Show |
C | 29 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(26): Show | 35 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.343-2409_343-2392d others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380292
|
CTTTTTTT others(12): Show |
C | 3 | a0002c0002t0002g0046a0002c0002t0004g0265a0002c0002t0004g0266 | 3 | HG02165.hp2 HG02451.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.343-2410_343-2392d others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | |||||
chr16:71380387
|
C | T | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-2332C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380387 | ||||||
chr16:71380456
|
GCAC | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 134 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.343-2256_343-2254d others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380456 | |||||
chr16:71380536
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 151 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.343-2183G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380536 | ||||||
chr16:71380583
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0183 | 2 | HG00741.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.343-2136C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380583 | ||||||
chr16:71380676
|
C | G | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-2043C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380676 | ||||||
chr16:71380676
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.343-2043C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380676 | ||||||
chr16:71380706
|
C | A | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-2013C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380706 | ||||||
chr16:71381012
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0357 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.343-1707G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381012 | ||||||
chr16:71381029
|
G | A | 21 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(18): Show | 27 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-1690G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381029 | ||||||
chr16:71381037
|
G | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(166): Show | 193 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.343-1682G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381037 | ||||||
chr16:71381209
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1510G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381209 | ||||||
chr16:71381210
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1509G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381210 | ||||||
chr16:71381213
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1506A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381213 | ||||||
chr16:71381215
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1504G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381215 | ||||||
chr16:71381216
|
TCATATTT others(56): Show |
T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1502_343-1440d others(65): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381216 | ||||||
chr16:71381282
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1437G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381282 | ||||||
chr16:71381286
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1433T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381286 | ||||||
chr16:71381288
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1431T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381288 | ||||||
chr16:71381292
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1427A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381292 | ||||||
chr16:71381297
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1422G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381297 | ||||||
chr16:71381303
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1416G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381303 | ||||||
chr16:71381304
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1415G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381304 | ||||||
chr16:71381307
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1412T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381307 | ||||||
chr16:71381308
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1411T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381308 | ||||||
chr16:71381310
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1409T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381310 | ||||||
chr16:71381311
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1408T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381311 | ||||||
chr16:71381313
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1406T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381313 | ||||||
chr16:71381314
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1405G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381314 | ||||||
chr16:71381319
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1400G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381319 | ||||||
chr16:71381320
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1399A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381320 | ||||||
chr16:71381321
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1398A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381321 | ||||||
chr16:71381327
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1392A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381327 | ||||||
chr16:71381328
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0002g0321 | 2 | HG00639.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.343-1391C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381328 | ||||||
chr16:71381329
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1390T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381329 | ||||||
chr16:71381331
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1388T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381331 | ||||||
chr16:71381333
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1386G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381333 | ||||||
chr16:71381336
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1383A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381336 | ||||||
chr16:71381337
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1382T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381337 | ||||||
chr16:71381342
|
T | C | 2 | a0001c0001t0002g0310a0001c0001t0002g0320 | 2 | NA18959.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.343-1377T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381342 | ||||||
chr16:71381387
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1332G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381387 | ||||||
chr16:71381409
|
C | CA | 47 | a0001c0001t0001g0159a0001c0001t0001g0185a0001c0001t0001g0187others(44): Show | 53 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.343-1294dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71381409 | |||||
chr16:71381409
|
CA | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(128): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.343-1294delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71381409 | |||||
chr16:71381491
|
A | G | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-1228A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381491 | ||||||
chr16:71381496
|
G | A | 89 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(86): Show | 93 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.343-1223G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381496 | ||||||
chr16:71381583
|
G | A | 7 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG00738.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-1136G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381583 | ||||||
chr16:71381603
|
A | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 224 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.343-1116A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381603 | ||||||
chr16:71381603
|
A | T | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.343-1116A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381603 | ||||||
chr16:71381682
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 134 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.343-1037G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381682 | ||||||
chr16:71381691
|
G | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | NA18942.hp2 NA18973.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1028G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381691 | ||||||
chr16:71381737
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.343-982G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381737 | ||||||
chr16:71381748
|
T | G | 35 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(32): Show | 41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-971T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381748 | ||||||
chr16:71381873
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.343-846C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381873 | ||||||
chr16:71381905
|
C | T | 20 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(17): Show | 21 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.343-814C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381905 | ||||||
chr16:71382016
|
A | AGAGGAG | 25 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(22): Show | 27 | HG00738.hp1 HG00741.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.343-681_343-676dup others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | |||||
chr16:71382016
|
A | AGAGGAGG others(2): Show |
57 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0159others(54): Show | 59 | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.343-684_343-676dup others(9): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | |||||
chr16:71382016
|
A | AGAGGAGG others(5): Show |
4 | a0001c0001t0001g0197a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG00597.hp1 HG00609.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-687_343-676dup others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | |||||
chr16:71382016
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.343-703A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382016 | ||||||
chr16:71382016
|
AGAG | A | 238 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.343-678_343-676del others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | |||||
chr16:71382026
|
G | A | 1 | a0001c0001t0002g0305 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.343-693G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382026 | ||||||
chr16:71382026
|
GAGGAGGA others(11): Show |
G | 1 | a0001c0001t0001g0141 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.343-678_343-661del others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382026 | |||||
chr16:71382032
|
GAGGAGGA others(5): Show |
G | 2 | a0001c0001t0001g0238a0001c0004t0001g0239 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.343-675_343-664del others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382032 | |||||
chr16:71382041
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-678G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382041 | ||||||
chr16:71382041
|
G | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18961.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.343-678G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382041 | ||||||
chr16:71382044
|
T | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0179a0001c0001t0002g0055others(2): Show | 5 | HG03225.hp1 NA18961.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-675T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382044 | ||||||
chr16:71382050
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-669G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382050 | ||||||
chr16:71382057
|
A | G | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18961.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.343-662A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382057 | ||||||
chr16:71382059
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-660A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382059 | ||||||
chr16:71382060
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-659G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382060 | ||||||
chr16:71382063
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-656G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382063 | ||||||
chr16:71382069
|
G | A | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0292 | 3 | NA18977.hp1 NA18994.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.343-650G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382069 | ||||||
chr16:71382117
|
G | C | 21 | a0002c0002t0001g0249a0002c0002t0001g0251a0002c0002t0001g0252others(18): Show | 27 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-602G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382117 | ||||||
chr16:71382122
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-597A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382122 | ||||||
chr16:71382124
|
A | AAAGGAAG others(9): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-576_343-561dup others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382124 | |||||
chr16:71382139
|
A | AGAAG | 4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0240others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-568_343-565dup others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382139 | |||||
chr16:71382139
|
A | AGAAGGAA others(27): Show |
1 | a0001c0001t0001g0179 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-561_343-560ins others(34): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382139 | |||||
chr16:71382139
|
A | AGAAGGAA others(27): Show |
87 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(84): Show | 91 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.343-561_343-560ins others(34): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382139 | |||||
chr16:71382155
|
A | AAGGAAGG others(47): Show |
4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(1): Show | 4 | HG02809.hp1 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-564_343-563ins others(54): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382155 | ||||||
chr16:71382155
|
A | AAGGAAGG others(11): Show |
158 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(155): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.343-564_343-563ins others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382155 | ||||||
chr16:71382155
|
A | AGAAGGAA others(9): Show |
1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.343-561_343-560ins others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382155 | |||||
chr16:71382155
|
A | AGAAGGAA others(13): Show |
10 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0267others(7): Show | 11 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.343-561_343-560ins others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382155 | |||||
chr16:71382155
|
A | AGAAGGAA others(17): Show |
2 | a0001c0001t0003g0054a0001c0001t0003g0264 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.343-561_343-560ins others(24): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382155 | |||||
chr16:71382155
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(8): Show | 13 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-564A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382155 | ||||||
chr16:71382161
|
T | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(183): Show | 208 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.343-558T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382161 | ||||||
chr16:71382162
|
A | G | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(2): Show | 5 | HG02809.hp1 HG03195.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-557A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382162 | ||||||
chr16:71382173
|
G | C | 1 | a0001c0001t0003g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.343-546G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382173 | ||||||
chr16:71382508
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.343-211C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382508 | ||||||
chr16:71382528
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 318 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.343-191T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382528 | ||||||
chr16:71382531
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0037others(4): Show | 9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.343-188C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382531 | ||||||
chr16:71382682
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.343-37C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382682 | ||||||
chr16:71382894
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.399+119C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71382894 | ||||||
chr16:71382934
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.399+159G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71382934 | ||||||
chr16:71382966
|
AT | A | 61 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0159others(58): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.399+194delT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 71382966 | |||||
chr16:71383003
|
C | T | 2 | a0001c0001t0003g0041a0001c0001t0003g0237 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.399+228C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383003 | ||||||
chr16:71383219
|
G | A | 12 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0054others(9): Show | 13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-148G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383219 | ||||||
chr16:71383228
|
G | A | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.400-139G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383228 | ||||||
chr16:71383241
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.400-126T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383241 | ||||||
chr16:71383323
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-44G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383323 | ||||||
chr16:71383325
|
A | ATGCACGA others(141): Show |
1 | a0002c0002t0002g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.400-41_477+29dupTG others(146): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 71383325 | |||||
chr16:71383330
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.400-37C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383330 | ||||||
chr16:71383476
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0240 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.477+32G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383476 | ||||||
chr16:71383492
|
C | T | 2 | a0001c0001t0001g0357a0001c0001t0001g0367 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.477+48C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383492 | ||||||
chr16:71383595
|
C | T | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 70 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.477+151C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383595 | ||||||
chr16:71383860
|
A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 92 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.478-110A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383860 | ||||||
chr16:71383880
|
C | T | 79 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 90 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.478-90C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383880 | ||||||
chr16:71383896
|
C | T | 2 | a0002c0002t0004g0265a0002c0002t0004g0266 | 2 | HG02165.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.478-74C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383896 | ||||||
chr16:71383939
|
A | G | 4 | a0001c0001t0001g0142a0002c0002t0001g0258a0002c0002t0001g0259others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-31A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383939 | ||||||
chr16:71384043
|
G | A | 2 | a0001c0001t0002g0333a0001c0001t0002g0334 | 2 | NA18952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.533+18G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 7/10 | chr16 | 71384043 | ||||||
chr16:71384388
|
T | C | 25 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 28 | HG00738.hp1 HG00741.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.573+10T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384388 | ||||||
chr16:71384524
|
A | G | 1 | a0002c0002t0002g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573+146A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384524 | ||||||
chr16:71384533
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.573+155A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384533 | ||||||
chr16:71384569
|
TA | T | 4 | a0001c0001t0001g0142a0002c0002t0001g0258a0002c0002t0001g0259others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+192delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384569 | ||||||
chr16:71384618
|
C | T | 1 | a0001c0001t0001g0368 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.574-165C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384618 | ||||||
chr16:71384659
|
CCACA | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 70 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.574-117_574-114del others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384659 | |||||
chr16:71384669
|
A | G | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 87 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.574-114A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384669 | ||||||
chr16:71384686
|
T | G | 94 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(91): Show | 98 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.574-97T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384686 | ||||||
chr16:71384687
|
G | GCACACAC others(1292): Show |
1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.574-78_574-77insCA others(1297): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1124): Show |
1 | a0002c0002t0002g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1129): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1261): Show |
1 | a0001c0001t0002g0351 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1266): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1263): Show |
1 | a0002c0002t0002g0028 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1268): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1272): Show |
30 | a0001c0001t0001g0142a0001c0001t0002g0192a0002c0002t0001g0258others(27): Show | 35 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1239): Show |
2 | a0001c0001t0002g0341a0001c0001t0002g0344 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1244): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1252): Show |
1 | a0001c0001t0002g0345 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1257): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1272): Show |
2 | a0001c0001t0002g0332a0001c0001t0002g0343 | 2 | NA18971.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1272): Show |
70 | a0001c0001t0001g0304a0001c0001t0001g0335a0001c0001t0001g0338others(67): Show | 92 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1261): Show |
1 | a0001c0001t0002g0346 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1266): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1286): Show |
1 | a0001c0001t0001g0352 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1270): Show |
1 | a0002c0002t0002g0254 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1275): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1272): Show |
1 | a0002c0002t0002g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1277): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0112a0001c0001t0001g0119 | 4 | NA18947.hp2 NA18967.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1282): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1285): Show |
1 | a0001c0001t0001g0367 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1290): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1272): Show |
1 | a0001c0001t0001g0357 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1240): Show |
2 | a0001c0001t0001g0194a0001c0001t0001g0223 | 2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1245): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1251): Show |
1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1256): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1249): Show |
1 | a0001c0001t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1254): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1256): Show |
1 | a0001c0001t0001g0232 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1234): Show |
1 | a0001c0001t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1239): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1256): Show |
80 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(77): Show | 84 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1258): Show |
2 | a0001c0001t0001g0229a0002c0002t0001g0251 | 2 | HG01081.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1263): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1256): Show |
1 | a0001c0001t0001g0219 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1256): Show |
4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0193others(1): Show | 4 | NA18997.hp2 NA19002.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1286): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0151 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1299): Show |
22 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0059others(19): Show | 23 | HG01168.hp1 HG01169.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1304): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1299): Show |
1 | a0001c0001t0001g0358 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1304): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1297): Show |
1 | a0001c0001t0001g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1302): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1275): Show |
3 | a0001c0001t0001g0263a0001c0001t0001g0274a0001c0001t0002g0273 | 3 | HG02809.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1280): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1301): Show |
1 | a0001c0001t0001g0298 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1306): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1263): Show |
1 | a0001c0001t0001g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1268): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1277): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0101 | 3 | HG01256.hp1 HG01258.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1282): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1290): Show |
1 | a0001c0001t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1295): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1288): Show |
40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(37): Show | 46 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1293): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1286): Show |
1 | a0001c0001t0001g0073 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1284): Show |
1 | a0001c0001t0001g0019 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1289): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1276): Show |
1 | a0001c0001t0003g0237 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1281): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1290): Show |
1 | a0001c0001t0003g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1295): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1288): Show |
2 | a0001c0001t0001g0236a0001c0001t0001g0240 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1293): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1237): Show |
1 | a0001c0001t0001g0122 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1242): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1284): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0261 | 3 | HG01515.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1289): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1280): Show |
54 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(51): Show | 63 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1285): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1280): Show |
1 | a0001c0001t0001g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1285): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1278): Show |
1 | a0001c0001t0001g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1283): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1278): Show |
1 | a0001c0001t0001g0130 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1283): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1297): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0083 | 2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1302): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1288): Show |
3 | a0001c0001t0001g0090a0001c0001t0001g0102a0001c0001t0001g0196 | 3 | NA19005.hp1 NA19010.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1293): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1252): Show |
1 | a0001c0001t0001g0234 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1257): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384687
|
G | GCACACAC others(1297): Show |
1 | a0001c0001t0001g0063 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-83_574-82insTA others(1302): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | |||||
chr16:71384692
|
C | CACCACAC others(1240): Show |
1 | a0001c0001t0003g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1245): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384692 | |||||
chr16:71384692
|
C | CACCACAC others(1258): Show |
11 | a0001c0001t0003g0030a0001c0001t0003g0035a0001c0001t0003g0053others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1263): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384692 | |||||
chr16:71384692
|
C | CACCACAC others(1238): Show |
1 | a0001c0001t0003g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1243): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384692 | |||||
chr16:71384694
|
C | CCACACAC others(1286): Show |
1 | a0001c0001t0001g0331 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384694 | |||||
chr16:71384856
|
T | C | 2 | a0001c0001t0002g0332a0001c0001t0002g0343 | 2 | NA18971.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.627+20T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384856 | ||||||
chr16:71384880
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.627+44C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384880 | ||||||
chr16:71384933
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0193others(1): Show | 4 | NA18997.hp2 NA19002.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+97G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384933 | ||||||
chr16:71384945
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.627+109C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384945 | ||||||
chr16:71385005
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(1): Show | 4 | HG02809.hp1 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+169G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385005 | ||||||
chr16:71385013
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.627+177A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385013 | ||||||
chr16:71385096
|
G | A | 19 | a0001c0001t0002g0192a0002c0002t0002g0006a0002c0002t0002g0012others(16): Show | 25 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.627+260G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385096 | ||||||
chr16:71385126
|
A | G | 2 | a0002c0002t0004g0265a0002c0002t0004g0266 | 2 | HG02165.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.627+290A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385126 | ||||||
chr16:71385199
|
T | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(260): Show | 287 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.627+363T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385199 | ||||||
chr16:71385204
|
A | G | 1 | a0001c0001t0002g0369 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.627+368A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385204 | ||||||
chr16:71385246
|
G | A | 2 | a0001c0001t0001g0357a0001c0001t0001g0367 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.628-331G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385246 | ||||||
chr16:71385327
|
T | C | 295 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(292): Show | 325 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.628-250T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385327 | ||||||
chr16:71385349
|
C | T | 93 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(90): Show | 97 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.628-228C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385349 | ||||||
chr16:71385466
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.628-111C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385466 | ||||||
chr16:71385691
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.699+43C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385691 | ||||||
chr16:71385692
|
A | G | 259 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 283 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.699+44A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385692 | ||||||
chr16:71385711
|
G | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0151 | 3 | HG00323.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.699+63G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385711 | ||||||
chr16:71385795
|
T | G | 1 | a0001c0001t0001g0366 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.699+147T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385795 | ||||||
chr16:71385932
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.699+284A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385932 | ||||||
chr16:71386264
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699+616C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386264 | ||||||
chr16:71386293
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.699+645G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386293 | ||||||
chr16:71386296
|
G | T | 2 | a0002c0002t0002g0158a0002c0002t0002g0279 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.699+648G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386296 | ||||||
chr16:71386367
|
AAGAG | A | 4 | a0001c0001t0001g0142a0002c0002t0001g0258a0002c0002t0001g0259others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+723_699+726del others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71386367 | |||||
chr16:71386384
|
A | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18997.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.699+736A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386384 | ||||||
chr16:71386639
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.699+991G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386639 | ||||||
chr16:71386674
|
T | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(81): Show | 92 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.699+1026T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386674 | ||||||
chr16:71386808
|
C | T | 2 | a0001c0001t0001g0357a0001c0001t0001g0367 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.699+1160C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386808 | ||||||
chr16:71387022
|
G | T | 1 | a0001c0001t0001g0298 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.699+1374G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387022 | ||||||
chr16:71387112
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.699+1464T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387112 | ||||||
chr16:71387271
|
G | T | 1 | a0001c0001t0002g0315 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.699+1623G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387271 | ||||||
chr16:71387378
|
G | A | 2 | a0001c0001t0003g0237a0002c0002t0002g0253 | 2 | HG03017.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.699+1730G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387378 | ||||||
chr16:71387461
|
C | CT | 6 | a0001c0001t0001g0206a0001c0001t0001g0236a0001c0001t0001g0240others(3): Show | 6 | HG00639.hp1 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1826dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71387461 | |||||
chr16:71387486
|
T | A | 1 | a0001c0001t0001g0352 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.699+1838T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387486 | ||||||
chr16:71387486
|
T | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.699+1838T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387486 | ||||||
chr16:71387672
|
A | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(88): Show | 100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.699+2024A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387672 | ||||||
chr16:71387802
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.700-1947G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387802 | ||||||
chr16:71388124
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.700-1625G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388124 | ||||||
chr16:71388148
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.700-1601G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388148 | ||||||
chr16:71388183
|
G | GT | 88 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(85): Show | 97 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.700-1566_700-1565i others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388183 | ||||||
chr16:71388334
|
C | CA | 88 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(85): Show | 97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.700-1398dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388334 | |||||
chr16:71388334
|
CA | C | 36 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 44 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.700-1398delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388334 | |||||
chr16:71388342
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | HG01070.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.700-1401_700-1392d others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388342 | |||||
chr16:71388346
|
A | AAAAAAG | 11 | a0001c0001t0003g0030a0001c0001t0003g0053a0001c0001t0003g0264others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.700-1379_700-1374d others(8): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388346 | |||||
chr16:71388346
|
A | AAG | 79 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.700-1402_700-1401i others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388346 | |||||
chr16:71388431
|
C | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.700-1318C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388431 | ||||||
chr16:71388600
|
C | G | 94 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(91): Show | 98 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.700-1149C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388600 | ||||||
chr16:71388707
|
G | A | 2 | a0001c0001t0002g0305a0001c0001t0002g0351 | 2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.700-1042G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388707 | ||||||
chr16:71388819
|
T | TA | 14 | a0001c0001t0001g0111a0001c0001t0001g0160a0001c0001t0003g0030others(11): Show | 15 | HG01168.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.700-915dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388819 | |||||
chr16:71388819
|
TA | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.700-915delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388819 | |||||
chr16:71388820
|
A | T | 1 | a0002c0002t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.700-929A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388820 | ||||||
chr16:71388997
|
C | CA | 9 | a0001c0001t0002g0273a0001c0001t0002g0294a0001c0001t0002g0295others(6): Show | 9 | HG00597.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-732dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388997 | |||||
chr16:71388997
|
CA | C | 34 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0071others(31): Show | 35 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.700-732delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388997 | |||||
chr16:71388997
|
CAA | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(235): Show | 261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.700-733_700-732del others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388997 | |||||
chr16:71389055
|
A | G | 274 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(271): Show | 298 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.700-694A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389055 | ||||||
chr16:71389187
|
C | CAAAATAA others(2): Show |
85 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 94 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.700-547_700-539dup others(9): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71389187 | |||||
chr16:71389254
|
G | C | 1 | a0001c0001t0002g0307 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.700-495G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389254 | ||||||
chr16:71389584
|
C | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(32): Show | 44 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.700-165C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389584 | ||||||
chr16:71389657
|
T | A | 1 | a0001c0001t0002g0308 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.700-92T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389657 |