geneid | 10487 |
---|---|
ensemblid | ENSG00000131236.18 |
hgncid | 20040 |
symbol | CAP1 |
name | cyclase associated actin cytoskeleton regulatory protein 1 |
refseq_nuc | NM_006367.4 |
refseq_prot | NP_006358.2 |
ensembl_nuc | ENST00000372805.8 |
ensembl_prot | ENSP00000361891.3 |
mane_status | MANE Select |
chr | chr1 |
start | 40040729 |
end | 40072648 |
strand | + |
ver | v1.2 |
region | chr1:40040729-40072648 |
region5000 | chr1:40035729-40077648 |
regionname0 | CAP1_chr1_40040729_40072648 |
regionname5000 | CAP1_chr1_40035729_40077648 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 475 | 374 | 96 | 46 | 174 | 16 | 41 | 138 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0002 | 0/0 | 475 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0003 | 1/0 | 475 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0004 | 0/0 | 475 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1428 | 360 | 82 | 46 | 174 | 16 | 41 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0002 | 0/0 | 1428 | 9 | 9 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0003 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0004 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0005 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0006 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0007 | 1/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
c0008 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1200 | 126 | 29 | 17 | 54 | 6 | 19 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0002 | 0/0 | 1201 | 68 | 10 | 5 | 40 | 3 | 10 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0003 | 0/0 | 1200 | 63 | 9 | 4 | 42 | 1 | 7 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0004 | 1/0 | 1199 | 59 | 21 | 14 | 16 | 3 | 4 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0005 | 0/0 | 1201 | 12 | 12 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0006 | 0/0 | 1200 | 11 | 0 | 1 | 9 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0007 | 0/0 | 1198 | 5 | 0 | 2 | 0 | 3 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0008 | 0/0 | 1200 | 4 | 0 | 0 | 4 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0009 | 0/0 | 1200 | 4 | 1 | 1 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0010 | 0/0 | 1201 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0011 | 0/0 | 1201 | 4 | 2 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0012 | 0/0 | 1201 | 3 | 1 | 0 | 1 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0013 | 0/0 | 1199 | 3 | 3 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0014 | 0/0 | 1200 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0015 | 0/0 | 1199 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0016 | 0/0 | 1201 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0017 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0018 | 0/0 | 1201 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0019 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0020 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0021 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0022 | 0/0 | 1201 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
t0023 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 28 | 3 | 3 | 14 | 0 | 8 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0002 | 0/0 | 23 | 0 | 2 | 14 | 2 | 5 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0003 | 0/0 | 13 | 0 | 6 | 4 | 3 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0008 | 0/0 | 5 | 1 | 0 | 2 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0017 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0031 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1428 | 360 | 82 | 46 | 174 | 16 | 41 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0002 | 0/0 | 1428 | 9 | 9 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0003 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0005 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0008 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0002c0004 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0003c0007 | 1/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0004c0006 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2627 | 124 | 28 | 17 | 54 | 6 | 18 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0002 | 0/0 | 2628 | 68 | 10 | 5 | 40 | 3 | 10 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0003 | 0/0 | 2627 | 63 | 9 | 4 | 42 | 1 | 7 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0004 | 0/0 | 2626 | 53 | 16 | 14 | 16 | 3 | 4 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0005 | 0/0 | 2628 | 11 | 11 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0006 | 0/0 | 2627 | 11 | 0 | 1 | 9 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0007 | 0/0 | 2625 | 5 | 0 | 2 | 0 | 3 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0008 | 0/0 | 2627 | 4 | 0 | 0 | 4 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0009 | 0/0 | 2627 | 4 | 1 | 1 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0011 | 0/0 | 2628 | 4 | 2 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0012 | 0/0 | 2628 | 3 | 1 | 0 | 1 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0014 | 0/0 | 2627 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0016 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0017 | 0/0 | 2627 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0018 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0019 | 0/0 | 2627 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0020 | 0/0 | 2627 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0021 | 0/0 | 2627 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0022 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0001t0023 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0002t0010 | 0/0 | 2628 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0002t0013 | 0/0 | 2626 | 3 | 3 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0002t0015 | 0/0 | 2626 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0003t0004 | 0/0 | 2626 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0005t0004 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0005t0005 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0001c0008t0001 | 0/0 | 2627 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0002c0004t0004 | 0/0 | 2626 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0003c0007t0004 | 1/0 | 2626 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
a0004c0006t0001 | 0/0 | 2627 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | copy fasta | chr1 | 40035729 | 40077648 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 25 | 3 | 3 | 12 | 0 | 7 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0031 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0002 | 0/0 | 22 | 0 | 2 | 13 | 2 | 5 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0003 | 0/0 | 9 | 0 | 6 | 2 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0017 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0006g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0006g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0007g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0009g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0011g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0012g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0012g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0014g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0018g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0019g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0021g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0022g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0001t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0002t0010g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0002t0010g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0002t0013g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0002t0013g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0002t0015g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0003t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0003t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0005t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0005t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0001c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0002c0004t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0003c0007t0004g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
a0004c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0003 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0166 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0168 | EUR | FIN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00423 | hp2 | a0001 | c0001 | t0016 | g0007 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01071 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0144 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01496 | hp1 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0003 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0003 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01891 | hp1 | a0001 | c0005 | t0005 | g0022 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG01981 | hp2 | a0001 | c0001 | t0009 | g0167 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02055 | hp2 | a0001 | c0005 | t0004 | g0064 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02145 | hp2 | a0001 | c0002 | t0013 | g0048 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02257 | hp1 | a0001 | c0001 | t0021 | g0183 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0058 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02622 | hp1 | a0001 | c0002 | t0010 | g0046 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02647 | hp1 | a0002 | c0004 | t0004 | g0039 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02717 | hp1 | a0001 | c0002 | t0010 | g0047 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0139 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02723 | hp1 | a0001 | c0002 | t0013 | g0048 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02723 | hp2 | a0001 | c0002 | t0015 | g0045 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02738 | hp1 | a0001 | c0001 | t0012 | g0191 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02809 | hp2 | a0001 | c0002 | t0015 | g0045 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0137 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02922 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03098 | hp1 | a0001 | c0002 | t0010 | g0047 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0013 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0038 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03579 | hp1 | a0001 | c0008 | t0001 | g0187 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0172 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0161 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03927 | hp1 | a0004 | c0006 | t0001 | g0001 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0066 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18949 | hp1 | a0001 | c0001 | t0018 | g0224 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18949 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18950 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18954 | hp1 | a0001 | c0001 | t0012 | g0228 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18956 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18960 | hp2 | a0001 | c0001 | t0019 | g0230 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18993 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19003 | hp2 | a0001 | c0001 | t0008 | g0219 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19030 | hp2 | a0001 | c0001 | t0023 | g0054 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19043 | hp1 | a0001 | c0002 | t0010 | g0046 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19057 | hp1 | a0001 | c0001 | t0020 | g0194 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19059 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19064 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19068 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19085 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ASW | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0158 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0184 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | GIH | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02559 | hp1 | a0001 | c0001 | t0014 | g0038 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA18955 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20300 | hp1 | a0001 | c0002 | t0013 | g0226 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
NA21309 | hp2 | a0002 | c0004 | t0004 | g0039 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
homoSapiens_grch38 | hp1 | a0003 | c0007 | t0004 | g0165 | REF | REF | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40067594
|
T | G | 3 | a0001a0002a0004 | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.685T>G | p.Cys229Gly | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 768/2626 | 685/1428 | 229/475 | chr1 | 40067594 | ||
chr1:40067615
|
T | G | 3 | a0001a0002a0004 | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.706T>G | p.Cys236Gly | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 789/2626 | 706/1428 | 236/475 | chr1 | 40067615 | ||
chr1:40067643
|
T | G | 3 | a0001a0002a0004 | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.734T>G | p.Ile245Ser | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 817/2626 | 734/1428 | 245/475 | chr1 | 40067643 | ||
chr1:40067648
|
T | G | 3 | a0001a0002a0004 | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.739T>G | p.Cys247Gly | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 822/2626 | 739/1428 | 247/475 | chr1 | 40067648 | ||
chr1:40067654
|
T | G | 3 | a0001a0002a0004 | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.745T>G | p.Tyr249Asp | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 828/2626 | 745/1428 | 249/475 | chr1 | 40067654 | ||
chr1:40067675
|
T | G | 3 | a0001a0002a0004 | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
missense_variant | MODERATE | c.766T>G | p.Ser256Ala | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 849/2626 | 766/1428 | 256/475 | chr1 | 40067675 | ||
chr1:40069786
|
C | T | 1 | a0004 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.905C>T | p.Ala302Val | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/13 | 988/2626 | 905/1428 | 302/475 | chr1 | 40069786 | ||
chr1:40070264
|
A | G | 1 | a0002 | 2 | HG02647.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1099A>G | p.Ile367Val | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/13 | 1182/2626 | 1099/1428 | 367/475 | chr1 | 40070264 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40059439
|
T | C | 2 | a0001c0003a0002c0004 | 4 | HG02647.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.93T>C | p.Tyr31Tyr | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/13 | 176/2626 | 93/1428 | 31/475 | chr1 | 40059439 | ||
chr1:40061737
|
G | A | 1 | a0001c0002 | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.219G>A | p.Ala73Ala | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/13 | 302/2626 | 219/1428 | 73/475 | chr1 | 40061737 | ||
chr1:40067587
|
C | T | 1 | a0001c0008 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.678C>T | p.Ala226Ala | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 761/2626 | 678/1428 | 226/475 | chr1 | 40067587 | ||
chr1:40070281
|
A | T | 1 | a0001c0005 | 2 | HG01891.hp1 HG02055.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1116A>T | p.Val372Val | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/13 | 1199/2626 | 1116/1428 | 372/475 | chr1 | 40070281 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40040753
|
G | C | 2 | a0001c0001t0006a0001c0001t0016 | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-59G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18594 | chr1 | 40040753 | |||||
chr1:40040758
|
G | C | 1 | a0001c0001t0017 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18589 | chr1 | 40040758 | |||||
chr1:40040779
|
C | G | 1 | a0001c0002t0013 | 3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-33C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18568 | chr1 | 40040779 | |||||
chr1:40040782
|
A | G | 2 | a0001c0001t0011a0001c0001t0023 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-30A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18565 | chr1 | 40040782 | |||||
chr1:40071536
|
G | A | 2 | a0001c0001t0008a0001c0001t0018 | 5 | NA18949.hp1 NA18993.hp2 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 3 | chr1 | 40071536 | |||||
chr1:40071759
|
TC | T | 1 | a0001c0001t0007 | 5 | HG00140.hp1 HG00735.hp2 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*227delC | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 227 | chr1 | 40071759 | |||||
chr1:40071893
|
C | T | 2 | a0001c0001t0006a0001c0001t0016 | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*360C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 360 | chr1 | 40071893 | |||||
chr1:40071944
|
A | G | 3 | a0001c0002t0010a0001c0002t0013a0001c0002t0015 | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*411A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 411 | chr1 | 40071944 | |||||
chr1:40071991
|
C | T | 1 | a0001c0001t0022 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 458 | chr1 | 40071991 | |||||
chr1:40072118
|
A | G | 1 | a0001c0001t0014 | 2 | HG02559.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*585A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 585 | chr1 | 40072118 | |||||
chr1:40072252
|
G | GA | 3 | a0001c0001t0006a0001c0001t0009a0001c0001t0019 | 16 | HG01496.hp1 HG01981.hp2 HG02027.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*738dupA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 739 | INFO_REALIGN_3_PRIME | chr1 | 40072252 | ||||
chr1:40072252
|
G | GAA | 5 | a0001c0001t0005a0001c0001t0011a0001c0001t0016others(2): Show | 21 | HG00423.hp2 HG01071.hp1 HG01243.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*737_*738dupAA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 739 | INFO_REALIGN_3_PRIME | chr1 | 40072252 | ||||
chr1:40072268
|
A | AAC | 4 | a0001c0001t0002a0001c0001t0012a0001c0001t0018others(1): Show | 73 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*736_*737insCA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 737 | INFO_REALIGN_3_PRIME | chr1 | 40072268 | ||||
chr1:40072268
|
A | AC | 9 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(6): Show | 198 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*735_*736insC | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 736 | chr1 | 40072268 | |||||
chr1:40072311
|
C | T | 1 | a0001c0001t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 778 | chr1 | 40072311 | |||||
chr1:40072429
|
G | A | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(4): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 896 | chr1 | 40072429 | |||||
chr1:40072555
|
C | G | 1 | a0001c0001t0020 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1022C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 1022 | chr1 | 40072555 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40040843
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0002g0049 | 2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-11+42G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40040843 | ||||||
chr1:40040862
|
G | T | 65 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(62): Show | 84 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11+61G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40040862 | ||||||
chr1:40040918
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | NA18960.hp1 NA18964.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-11+117G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40040918 | ||||||
chr1:40041053
|
G | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+252G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041053 | ||||||
chr1:40041058
|
G | C | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+257G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041058 | ||||||
chr1:40041126
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-11+325C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041126 | ||||||
chr1:40041440
|
C | G | 5 | a0001c0001t0003g0227a0001c0001t0003g0229a0001c0001t0003g0231others(2): Show | 5 | NA18950.hp1 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+639C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041440 | ||||||
chr1:40041473
|
C | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+672C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041473 | ||||||
chr1:40041477
|
C | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+676C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041477 | ||||||
chr1:40041496
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+695A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041496 | ||||||
chr1:40041520
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-11+719A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041520 | ||||||
chr1:40041550
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(200): Show | 321 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.-11+749G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041550 | ||||||
chr1:40041552
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-11+751G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041552 | ||||||
chr1:40041718
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11+917T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041718 | ||||||
chr1:40041734
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0140others(2): Show | 12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+933G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041734 | ||||||
chr1:40041892
|
G | A | 7 | a0001c0001t0003g0042a0001c0001t0003g0178a0001c0001t0003g0179others(4): Show | 8 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1091G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041892 | ||||||
chr1:40041978
|
C | G | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+1177C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041978 | ||||||
chr1:40042033
|
T | TTTAA | 86 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(83): Show | 116 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11+1235_-11+1238d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40042033 | |||||
chr1:40042074
|
G | A | 1 | a0001c0001t0004g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+1273G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042074 | ||||||
chr1:40042186
|
G | T | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+1385G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042186 | ||||||
chr1:40042245
|
G | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+1444G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042245 | ||||||
chr1:40042374
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11+1573A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042374 | ||||||
chr1:40042394
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-11+1593G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042394 | ||||||
chr1:40042649
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-11+1848T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042649 | ||||||
chr1:40042673
|
G | T | 2 | a0001c0002t0013g0048a0001c0002t0013g0226 | 3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-11+1872G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042673 | ||||||
chr1:40042733
|
G | A | 12 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(9): Show | 15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+1932G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042733 | ||||||
chr1:40043162
|
AAAG | A | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+2362_-11+2364d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043162 | ||||||
chr1:40043195
|
T | TTTTG | 2 | a0001c0001t0002g0014a0001c0001t0002g0069 | 4 | HG02027.hp2 NA18952.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+2410_-11+2413d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40043195 | |||||
chr1:40043415
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 315 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.-11+2614T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043415 | ||||||
chr1:40043424
|
C | CT | 60 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(57): Show | 75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+2624dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40043424 | |||||
chr1:40043494
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-11+2693C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043494 | ||||||
chr1:40043596
|
G | C | 4 | a0001c0001t0003g0042a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 5 | HG02559.hp2 HG02965.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2795G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043596 | ||||||
chr1:40043618
|
T | C | 1 | a0001c0002t0015g0045 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-11+2817T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043618 | ||||||
chr1:40043634
|
T | G | 1 | a0001c0001t0004g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11+2833T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043634 | ||||||
chr1:40043737
|
C | T | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+2936C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043737 | ||||||
chr1:40043874
|
C | CA | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(106): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.-11+3083dupA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40043874 | |||||
chr1:40044224
|
C | G | 5 | a0001c0001t0004g0062a0001c0001t0005g0022a0001c0001t0005g0063others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+3423C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044224 | ||||||
chr1:40044236
|
GA | G | 3 | a0001c0001t0011g0013a0001c0001t0011g0055a0001c0001t0023g0054 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+3445delA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044236 | |||||
chr1:40044348
|
A | C | 1 | a0001c0001t0004g0175 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11+3547A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044348 | ||||||
chr1:40044620
|
A | G | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+3819A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044620 | ||||||
chr1:40044705
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+3904C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044705 | ||||||
chr1:40044760
|
C | T | 18 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(15): Show | 27 | HG00423.hp2 HG01496.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11+3959C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044760 | ||||||
chr1:40044788
|
C | CT | 30 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0125others(27): Show | 34 | HG01243.hp2 HG01433.hp1 HG01978.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+4013dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | |||||
chr1:40044788
|
CT | C | 49 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(46): Show | 87 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11+4013delT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | |||||
chr1:40044788
|
CTT | C | 55 | a0001c0001t0002g0086a0001c0001t0003g0006a0001c0001t0003g0019others(52): Show | 72 | HG00408.hp2 HG01071.hp1 HG01175.hp1 others(69): Show |
intron_variant | MODIFIER | c.-11+4012_-11+4013d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | |||||
chr1:40044788
|
CTTT | C | 7 | a0001c0001t0003g0185a0001c0001t0003g0186a0001c0002t0010g0046others(4): Show | 11 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+4011_-11+4013d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | |||||
chr1:40044788
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0007g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-11+4003_-11+4013d others(13): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | |||||
chr1:40044803
|
T | A | 1 | a0001c0001t0003g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+4002T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044803 | ||||||
chr1:40044858
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+4057A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044858 | ||||||
chr1:40044928
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11+4127C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044928 | ||||||
chr1:40044931
|
G | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+4130G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044931 | ||||||
chr1:40044946
|
G | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+4145G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044946 | ||||||
chr1:40044987
|
G | A | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+4186G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044987 | ||||||
chr1:40045035
|
C | T | 1 | a0001c0008t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11+4234C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045035 | ||||||
chr1:40045036
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | NA18969.hp1 NA18970.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-11+4235G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045036 | ||||||
chr1:40045216
|
T | C | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+4415T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045216 | ||||||
chr1:40045255
|
G | A | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+4454G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045255 | ||||||
chr1:40045317
|
C | T | 60 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(57): Show | 75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+4516C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045317 | ||||||
chr1:40045340
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-11+4539G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045340 | ||||||
chr1:40045350
|
G | A | 4 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190others(1): Show | 4 | NA18943.hp2 NA18947.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+4549G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045350 | ||||||
chr1:40045372
|
A | G | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+4571A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045372 | ||||||
chr1:40045467
|
T | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+4666T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045467 | ||||||
chr1:40045586
|
T | C | 3 | a0001c0001t0011g0013a0001c0001t0011g0055a0001c0001t0023g0054 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+4785T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045586 | ||||||
chr1:40045595
|
G | A | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+4794G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045595 | ||||||
chr1:40045627
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11+4826C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045627 | ||||||
chr1:40045842
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+5041T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045842 | ||||||
chr1:40045843
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+5042G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045843 | ||||||
chr1:40045848
|
C | T | 1 | a0001c0001t0003g0220 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-11+5047C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045848 | ||||||
chr1:40045894
|
C | T | 1 | a0001c0001t0002g0014 | 3 | HG02027.hp2 NA18952.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-11+5093C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045894 | ||||||
chr1:40045968
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11+5167A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045968 | ||||||
chr1:40046253
|
C | T | 1 | a0001c0001t0004g0168 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-11+5452C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046253 | ||||||
chr1:40046321
|
T | C | 1 | a0001c0001t0011g0055 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11+5520T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046321 | ||||||
chr1:40046430
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+5629G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046430 | ||||||
chr1:40046474
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11+5673A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046474 | ||||||
chr1:40046480
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(198): Show | 319 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.-11+5688delA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40046480 | |||||
chr1:40046492
|
A | G | 1 | a0001c0003t0004g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-11+5691A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046492 | ||||||
chr1:40046510
|
A | G | 7 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(4): Show | 10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+5709A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046510 | ||||||
chr1:40046565
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-11+5764G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046565 | ||||||
chr1:40046589
|
C | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+5788C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046589 | ||||||
chr1:40046711
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0002g0049 | 2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-11+5910A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046711 | ||||||
chr1:40046773
|
C | CT | 6 | a0001c0001t0002g0081a0001c0001t0003g0180a0001c0001t0003g0225others(3): Show | 6 | HG00597.hp1 HG00597.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+5989dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40046773 | |||||
chr1:40046773
|
CT | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0097a0001c0001t0002g0067others(4): Show | 8 | HG02258.hp2 HG02273.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+5989delT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40046773 | |||||
chr1:40046836
|
G | A | 3 | a0001c0001t0005g0022a0001c0005t0004g0064a0001c0005t0005g0022 | 3 | HG01891.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-11+6035G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046836 | ||||||
chr1:40046919
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(76): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+6118C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046919 | ||||||
chr1:40046926
|
C | A | 1 | a0001c0001t0003g0222 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-11+6125C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046926 | ||||||
chr1:40047062
|
C | T | 1 | a0001c0001t0014g0038 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11+6261C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047062 | ||||||
chr1:40047101
|
TTATAATC others(39): Show |
T | 86 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(83): Show | 116 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11+6316_-11+6361d others(48): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40047101 | |||||
chr1:40047192
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11+6391A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047192 | ||||||
chr1:40047433
|
C | A | 1 | a0001c0001t0012g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11+6632C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047433 | ||||||
chr1:40047649
|
C | T | 60 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(57): Show | 75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+6848C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047649 | ||||||
chr1:40047700
|
T | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+6899T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047700 | ||||||
chr1:40047770
|
C | T | 1 | a0001c0001t0009g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+6969C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047770 | ||||||
chr1:40047880
|
G | A | 4 | a0001c0001t0003g0042a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 5 | HG02559.hp2 HG02965.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+7079G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047880 | ||||||
chr1:40048038
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(74): Show | 130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-11+7237T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048038 | ||||||
chr1:40048162
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-11+7361G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048162 | ||||||
chr1:40048314
|
ATTACAGG others(21): Show |
A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7543_-11+7570d others(30): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40048314 | |||||
chr1:40048394
|
A | C | 60 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(57): Show | 75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+7593A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048394 | ||||||
chr1:40048470
|
T | C | 1 | a0001c0008t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11+7669T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048470 | ||||||
chr1:40048489
|
G | A | 2 | a0001c0001t0011g0013a0001c0001t0011g0055 | 4 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+7688G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048489 | ||||||
chr1:40048659
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7858T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048659 | ||||||
chr1:40048673
|
T | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7872T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048673 | ||||||
chr1:40048693
|
T | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7892T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048693 | ||||||
chr1:40048752
|
C | A | 1 | a0001c0008t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11+7951C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048752 | ||||||
chr1:40048872
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8071T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048872 | ||||||
chr1:40048997
|
A | G | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+8196A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048997 | ||||||
chr1:40049178
|
A | AT | 40 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0050others(37): Show | 75 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+8403dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATT | 63 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(60): Show | 114 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-11+8402_-11+8403d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTT | 23 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0093others(20): Show | 34 | HG00408.hp2 HG00423.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+8401_-11+8403d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTT | 6 | a0001c0001t0001g0123a0001c0001t0004g0062a0001c0001t0005g0060others(3): Show | 8 | HG00741.hp2 HG01496.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+8400_-11+8403d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTT | 4 | a0001c0001t0005g0063a0001c0002t0010g0046a0001c0002t0015g0045others(1): Show | 6 | HG02055.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+8399_-11+8403d others(7): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTT | 4 | a0001c0001t0005g0022a0001c0002t0010g0047a0001c0002t0013g0048others(1): Show | 6 | HG01891.hp1 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+8398_-11+8403d others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0003g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-11+8392_-11+8403d others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(6): Show |
25 | a0001c0001t0003g0006a0001c0001t0003g0043a0001c0001t0003g0179others(22): Show | 34 | HG02280.hp1 HG03017.hp1 HG03209.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+8391_-11+8403d others(15): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(7): Show |
14 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0206others(11): Show | 18 | HG00597.hp2 HG01175.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11+8390_-11+8403d others(16): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(8): Show |
6 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0003g0216others(3): Show | 6 | HG01175.hp2 HG02135.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+8389_-11+8403d others(17): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0003g0044a0001c0001t0012g0191 | 3 | HG02738.hp1 NA19007.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-11+8388_-11+8403d others(18): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0003g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-11+8387_-11+8403d others(19): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0003g0190a0001c0001t0003g0218 | 2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11+8386_-11+8403d others(20): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049178
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-11+8392_-11+8403d others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | |||||
chr1:40049226
|
G | A | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+8425G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049226 | ||||||
chr1:40049269
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(76): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+8468C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049269 | ||||||
chr1:40049351
|
C | A | 2 | a0001c0002t0010g0046a0001c0002t0010g0047 | 4 | HG02622.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+8550C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049351 | ||||||
chr1:40049362
|
C | T | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+8561C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049362 | ||||||
chr1:40049374
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8573T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049374 | ||||||
chr1:40049453
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8652T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049453 | ||||||
chr1:40049605
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(198): Show | 319 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.-11+8804G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049605 | ||||||
chr1:40049615
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-11+8814C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049615 | ||||||
chr1:40049674
|
T | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8873T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049674 | ||||||
chr1:40049685
|
T | G | 1 | a0001c0001t0003g0196 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-11+8884T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049685 | ||||||
chr1:40049710
|
C | T | 3 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0015g0045 | 6 | HG02622.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+8909C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049710 | ||||||
chr1:40049724
|
C | A | 60 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(57): Show | 75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+8923C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049724 | ||||||
chr1:40049747
|
C | T | 7 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(4): Show | 10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+8946C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049747 | ||||||
chr1:40049776
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-11+8975T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049776 | ||||||
chr1:40050064
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11+9263A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050064 | ||||||
chr1:40050109
|
C | G | 1 | a0001c0001t0007g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10-9228C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050109 | ||||||
chr1:40050405
|
T | TGAAATAT others(106): Show |
237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(234): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-10-8922_-10-8921i others(115): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050405 | |||||
chr1:40050405
|
T | TGAAATAT others(106): Show |
5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-8922_-10-8921i others(115): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050405 | |||||
chr1:40050407
|
A | AAATATCT others(106): Show |
1 | a0001c0001t0003g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10-8922_-10-8921i others(115): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050407 | |||||
chr1:40050520
|
G | A | 2 | a0001c0001t0001g0103a0001c0008t0001g0187 | 2 | HG02273.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-10-8817G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050520 | ||||||
chr1:40050528
|
G | A | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-8809G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050528 | ||||||
chr1:40050566
|
G | A | 2 | a0001c0001t0004g0010a0001c0001t0005g0010 | 4 | HG03195.hp2 HG06807.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-8771G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050566 | ||||||
chr1:40050724
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-10-8613A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050724 | ||||||
chr1:40050768
|
CTCCACA | C | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-8565_-10-8560d others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050768 | |||||
chr1:40050846
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-10-8491T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050846 | ||||||
chr1:40051395
|
TAC | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(78): Show | 137 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-10-7926_-10-7925d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40051395 | |||||
chr1:40051395
|
TACAC | T | 65 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(62): Show | 84 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(81): Show |
intron_variant | MODIFIER | c.-10-7928_-10-7925d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40051395 | |||||
chr1:40051482
|
G | T | 1 | a0001c0001t0007g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10-7855G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051482 | ||||||
chr1:40051494
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0140others(2): Show | 12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-7843A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051494 | ||||||
chr1:40051529
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-10-7808G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051529 | ||||||
chr1:40051566
|
G | T | 69 | a0001c0001t0001g0117a0001c0001t0003g0006a0001c0001t0003g0019others(66): Show | 90 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(87): Show |
intron_variant | MODIFIER | c.-10-7771G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051566 | ||||||
chr1:40051575
|
T | G | 1 | a0001c0001t0001g0094 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-10-7762T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051575 | ||||||
chr1:40051626
|
A | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7711A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051626 | ||||||
chr1:40051629
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-10-7708G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051629 | ||||||
chr1:40051640
|
A | T | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-7697A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051640 | ||||||
chr1:40051692
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-10-7645C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051692 | ||||||
chr1:40051696
|
C | T | 4 | a0001c0001t0005g0021a0001c0001t0005g0058a0001c0001t0005g0060others(1): Show | 5 | HG02258.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-7641C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051696 | ||||||
chr1:40051742
|
A | ATT | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7588_-10-7587d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40051742 | |||||
chr1:40051773
|
G | A | 7 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(4): Show | 10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-7564G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051773 | ||||||
chr1:40051787
|
T | G | 1 | a0001c0001t0003g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-10-7550T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051787 | ||||||
chr1:40051794
|
C | T | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7543C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051794 | ||||||
chr1:40051828
|
C | G | 2 | a0001c0001t0004g0062a0001c0001t0005g0063 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-10-7509C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051828 | ||||||
chr1:40051844
|
C | T | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-7493C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051844 | ||||||
chr1:40051858
|
C | T | 1 | a0001c0001t0003g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-7479C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051858 | ||||||
chr1:40051880
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10-7457G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051880 | ||||||
chr1:40051907
|
A | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7430A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051907 | ||||||
chr1:40051945
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10-7392C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051945 | ||||||
chr1:40052066
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(73): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-10-7271T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052066 | ||||||
chr1:40052128
|
T | C | 2 | a0001c0001t0002g0072a0001c0001t0002g0083 | 2 | NA18971.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-10-7209T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052128 | ||||||
chr1:40052222
|
C | T | 1 | a0001c0001t0007g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10-7115C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052222 | ||||||
chr1:40052291
|
G | T | 1 | a0001c0001t0003g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-10-7046G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052291 | ||||||
chr1:40052431
|
G | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6906G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052431 | ||||||
chr1:40052438
|
C | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6899C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052438 | ||||||
chr1:40052494
|
G | A | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6843G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052494 | ||||||
chr1:40052572
|
A | G | 6 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(3): Show | 9 | HG02258.hp2 HG03195.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-6765A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052572 | ||||||
chr1:40052818
|
C | T | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6519C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052818 | ||||||
chr1:40052828
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG00099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-10-6509C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052828 | ||||||
chr1:40052829
|
G | A | 1 | a0001c0001t0003g0197 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-10-6508G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052829 | ||||||
chr1:40052985
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-6352G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052985 | ||||||
chr1:40053035
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(238): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-10-6302T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053035 | ||||||
chr1:40053080
|
C | T | 58 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(55): Show | 73 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(70): Show |
intron_variant | MODIFIER | c.-10-6257C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053080 | ||||||
chr1:40053165
|
A | G | 7 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(4): Show | 10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-6172A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053165 | ||||||
chr1:40053361
|
A | G | 1 | a0001c0001t0003g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-10-5976A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053361 | ||||||
chr1:40053391
|
A | G | 1 | a0001c0001t0003g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-10-5946A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053391 | ||||||
chr1:40053410
|
C | T | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5927C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053410 | ||||||
chr1:40053472
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 315 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.-10-5865T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053472 | ||||||
chr1:40053546
|
G | C | 3 | a0001c0001t0011g0013a0001c0001t0011g0055a0001c0001t0023g0054 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-5791G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053546 | ||||||
chr1:40053555
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5782A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053555 | ||||||
chr1:40053579
|
C | T | 3 | a0001c0001t0003g0212a0001c0001t0003g0215a0001c0001t0003g0216 | 3 | HG01175.hp2 HG01255.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-10-5758C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053579 | ||||||
chr1:40053631
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5706A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053631 | ||||||
chr1:40053647
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5690A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053647 | ||||||
chr1:40053681
|
A | T | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5656A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053681 | ||||||
chr1:40053725
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10-5612G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053725 | ||||||
chr1:40053727
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5610A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053727 | ||||||
chr1:40053851
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-10-5486A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053851 | ||||||
chr1:40053971
|
A | G | 1 | a0001c0008t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10-5366A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053971 | ||||||
chr1:40054061
|
T | TAAAAC | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-5259_-10-5255d others(7): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054061 | |||||
chr1:40054061
|
T | TAAAACAA others(3): Show |
1 | a0001c0001t0002g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-10-5264_-10-5255d others(12): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054061 | |||||
chr1:40054130
|
AGAGT | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(76): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-10-5202_-10-5199d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054130 | |||||
chr1:40054183
|
G | A | 1 | a0001c0001t0004g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-10-5154G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054183 | ||||||
chr1:40054193
|
C | CTTTTTTT others(3): Show |
50 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(47): Show | 65 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.-10-5139_-10-5130d others(12): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | |||||
chr1:40054193
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0210others(3): Show | 6 | HG01175.hp2 HG01255.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5140_-10-5130d others(13): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | |||||
chr1:40054193
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0211a0001c0001t0003g0216 | 2 | HG02300.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-10-5141_-10-5130d others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | |||||
chr1:40054193
|
CTTTTTT | C | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-5135_-10-5130d others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | |||||
chr1:40054222
|
A | G | 66 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(63): Show | 86 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.-10-5115A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054222 | ||||||
chr1:40054347
|
C | T | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-4990C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054347 | ||||||
chr1:40054415
|
A | G | 68 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(65): Show | 89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-4922A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054415 | ||||||
chr1:40054428
|
G | A | 1 | a0001c0001t0004g0145 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-10-4909G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054428 | ||||||
chr1:40054507
|
T | G | 1 | a0001c0001t0002g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-10-4830T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054507 | ||||||
chr1:40054519
|
G | C | 1 | a0001c0003t0004g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-4818G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054519 | ||||||
chr1:40054935
|
C | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-4402C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054935 | ||||||
chr1:40054938
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-4399G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054938 | ||||||
chr1:40054951
|
C | G | 1 | a0001c0001t0004g0163 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-4386C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054951 | ||||||
chr1:40055043
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-10-4294C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055043 | ||||||
chr1:40055102
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-4235G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055102 | ||||||
chr1:40055117
|
C | G | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-4220C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055117 | ||||||
chr1:40055120
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-10-4217A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055120 | ||||||
chr1:40055254
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-4083A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055254 | ||||||
chr1:40055259
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-10-4078G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055259 | ||||||
chr1:40055261
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-10-4076A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055261 | ||||||
chr1:40055335
|
TATC | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-3999_-10-3997d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40055335 | |||||
chr1:40055423
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-10-3914A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055423 | ||||||
chr1:40055446
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0086 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-10-3891A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055446 | ||||||
chr1:40055492
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-3845G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055492 | ||||||
chr1:40055663
|
T | C | 1 | a0001c0001t0004g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-10-3674T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055663 | ||||||
chr1:40055709
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-3628A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055709 | ||||||
chr1:40055722
|
T | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-3615T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055722 | ||||||
chr1:40055741
|
T | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-3596T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055741 | ||||||
chr1:40055845
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-3492A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055845 | ||||||
chr1:40056085
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-3252C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056085 | ||||||
chr1:40056159
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-10-3178C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056159 | ||||||
chr1:40056242
|
T | G | 1 | a0001c0001t0004g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-3095T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056242 | ||||||
chr1:40056279
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(73): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-10-3058C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056279 | ||||||
chr1:40056300
|
A | ATT | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(112): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.-10-3025_-10-3024d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40056300 | |||||
chr1:40056300
|
A | ATTT | 15 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0002g0081others(12): Show | 18 | HG00597.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-3026_-10-3024d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40056300 | |||||
chr1:40056776
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-2561A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056776 | ||||||
chr1:40056897
|
C | T | 1 | a0001c0001t0019g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-10-2440C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056897 | ||||||
chr1:40056915
|
A | AG | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-2422_-10-2421i others(3): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056915 | ||||||
chr1:40056915
|
A | C | 1 | a0001c0001t0004g0162 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-10-2422A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056915 | ||||||
chr1:40057012
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-10-2325G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057012 | ||||||
chr1:40057030
|
G | A | 12 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(9): Show | 15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-2307G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057030 | ||||||
chr1:40057258
|
T | G | 2 | a0001c0001t0007g0144a0001c0001t0007g0166 | 2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-10-2079T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057258 | ||||||
chr1:40057299
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-2038C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057299 | ||||||
chr1:40057410
|
T | C | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-1927T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057410 | ||||||
chr1:40057427
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0113 | 2 | HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-1910C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057427 | ||||||
chr1:40057444
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-1893A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057444 | ||||||
chr1:40057484
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0051others(5): Show | 12 | HG02040.hp1 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-1853A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057484 | ||||||
chr1:40057485
|
G | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-1852G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057485 | ||||||
chr1:40057561
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0113 | 2 | HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-1776T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057561 | ||||||
chr1:40057606
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-1731G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057606 | ||||||
chr1:40057656
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(109): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.-10-1681A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057656 | ||||||
chr1:40057806
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-10-1531C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057806 | ||||||
chr1:40058142
|
G | T | 1 | a0001c0001t0005g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10-1195G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058142 | ||||||
chr1:40058299
|
A | C | 3 | a0001c0001t0011g0013a0001c0001t0011g0055a0001c0001t0023g0054 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-1038A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058299 | ||||||
chr1:40058299
|
A | T | 29 | a0001c0001t0003g0020a0001c0001t0003g0043a0001c0001t0003g0184others(26): Show | 34 | HG01175.hp1 HG02015.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10-1038A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058299 | ||||||
chr1:40058497
|
G | T | 1 | a0001c0001t0003g0209 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-10-840G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058497 | ||||||
chr1:40058528
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-809C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058528 | ||||||
chr1:40058759
|
A | G | 12 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(9): Show | 15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-578A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058759 | ||||||
chr1:40058839
|
G | T | 3 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0015g0045 | 6 | HG02622.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-498G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058839 | ||||||
chr1:40058916
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0140others(2): Show | 12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-421G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058916 | ||||||
chr1:40058976
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-10-361C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058976 | ||||||
chr1:40059014
|
T | TTGCAAAT others(286): Show |
1 | a0001c0001t0021g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-10-305_-10-304ins others(293): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | |||||
chr1:40059014
|
T | TTGCAAAT others(299): Show |
22 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0042others(19): Show | 32 | HG00408.hp2 HG00597.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-305_-10-304ins others(306): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | |||||
chr1:40059014
|
T | TTGCAAAT others(299): Show |
1 | a0001c0008t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10-305_-10-304ins others(306): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | |||||
chr1:40059014
|
T | TTGCAAAT others(302): Show |
1 | a0001c0001t0003g0202 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-10-305_-10-304ins others(309): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | |||||
chr1:40059014
|
T | TTGCAAAT others(300): Show |
30 | a0001c0001t0003g0020a0001c0001t0003g0043a0001c0001t0003g0178others(27): Show | 35 | HG02015.hp1 HG02129.hp2 HG02135.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10-305_-10-304ins others(307): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | |||||
chr1:40059014
|
T | TTGCAAAT others(301): Show |
5 | a0001c0001t0003g0189a0001c0001t0003g0200a0001c0001t0003g0208others(2): Show | 5 | HG01175.hp1 HG04184.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-305_-10-304ins others(308): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | |||||
chr1:40059018
|
A | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-319A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40059018 | ||||||
chr1:40059194
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10-143T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40059194 | ||||||
chr1:40059274
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-63T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40059274 | ||||||
chr1:40059648
|
AACACAAG others(3): Show |
A | 4 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0103others(1): Show | 6 | HG01109.hp2 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+191_112+200del others(10): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/12 | chr1 | 40059648 | ||||||
chr1:40059754
|
A | G | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.112+296A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/12 | chr1 | 40059754 | ||||||
chr1:40059817
|
A | T | 1 | a0001c0001t0003g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-250A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/12 | chr1 | 40059817 | ||||||
chr1:40060321
|
G | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.216+151G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060321 | ||||||
chr1:40060331
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 315 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.216+161T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060331 | ||||||
chr1:40060344
|
G | A | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.216+174G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060344 | ||||||
chr1:40060636
|
C | T | 1 | a0001c0001t0003g0221 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.216+466C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060636 | ||||||
chr1:40060722
|
C | T | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+552C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060722 | ||||||
chr1:40060724
|
A | G | 8 | a0001c0001t0004g0158a0001c0001t0004g0159a0001c0001t0004g0160others(5): Show | 8 | HG00280.hp1 HG01109.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.216+554A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060724 | ||||||
chr1:40061013
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.217-722C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061013 | ||||||
chr1:40061156
|
C | CT | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(194): Show | 313 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.217-566dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 40061156 | |||||
chr1:40061211
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.217-524T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061211 | ||||||
chr1:40061338
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.217-397T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061338 | ||||||
chr1:40061363
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.217-372C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061363 | ||||||
chr1:40061448
|
C | T | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.217-287C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061448 | ||||||
chr1:40061540
|
C | T | 1 | a0001c0001t0006g0065 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.217-195C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061540 | ||||||
chr1:40061858
|
C | T | 3 | a0001c0001t0005g0022a0001c0005t0004g0064a0001c0005t0005g0022 | 3 | HG01891.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.294+46C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40061858 | ||||||
chr1:40062051
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.294+239T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062051 | ||||||
chr1:40062222
|
ACTCT | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.294+415_294+418del others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062222 | |||||
chr1:40062234
|
A | C | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.294+422A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062234 | ||||||
chr1:40062324
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.294+512G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062324 | ||||||
chr1:40062523
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0178 | 3 | HG02559.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.294+711G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062523 | ||||||
chr1:40062578
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0004g0040 | 2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.294+766C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062578 | ||||||
chr1:40062639
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.294+827C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062639 | ||||||
chr1:40062716
|
G | C | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.294+904G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062716 | ||||||
chr1:40062760
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.294+948C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062760 | ||||||
chr1:40062773
|
T | TTGTGTG | 113 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(110): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.294+981_294+986dup others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(1): Show |
14 | a0001c0001t0001g0033a0001c0001t0001g0111a0001c0001t0001g0113others(11): Show | 20 | HG00735.hp1 HG01071.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.294+979_294+986dup others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0002g0025a0001c0001t0023g0054 | 3 | HG03490.hp2 HG03492.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+977_294+986dup others(10): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(5): Show |
56 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(53): Show | 71 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(68): Show |
intron_variant | MODIFIER | c.294+975_294+986dup others(12): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(7): Show |
12 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0210others(9): Show | 19 | HG02129.hp2 HG02145.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.294+973_294+986dup others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(9): Show |
1 | a0001c0002t0013g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.294+971_294+986dup others(16): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(11): Show |
12 | a0001c0001t0004g0136a0001c0001t0004g0138a0001c0001t0004g0142others(9): Show | 13 | HG00280.hp1 HG01433.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.294+969_294+986dup others(18): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(13): Show |
7 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0153others(4): Show | 7 | HG01109.hp1 HG01981.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+967_294+986dup others(20): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(15): Show |
13 | a0001c0001t0004g0003a0001c0001t0004g0041a0001c0001t0004g0145others(10): Show | 24 | HG00099.hp2 HG00735.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.294+965_294+986dup others(22): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062773
|
T | TTGTGTGT others(17): Show |
2 | a0001c0001t0004g0156a0001c0001t0007g0166 | 2 | HG00140.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.294+963_294+986dup others(24): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | |||||
chr1:40062927
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.294+1115A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062927 | ||||||
chr1:40062953
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.294+1141C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062953 | ||||||
chr1:40062992
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(132): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.294+1180T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062992 | ||||||
chr1:40063005
|
A | T | 2 | a0001c0002t0013g0048a0001c0002t0013g0226 | 3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.294+1193A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063005 | ||||||
chr1:40063016
|
G | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.294+1204G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063016 | ||||||
chr1:40063194
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 315 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.295-1033C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063194 | ||||||
chr1:40063212
|
C | CT | 3 | a0001c0001t0008g0018a0001c0001t0008g0219a0001c0001t0018g0224 | 5 | NA18949.hp1 NA18993.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1014dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40063212 | |||||
chr1:40063246
|
C | T | 1 | a0001c0001t0004g0017 | 3 | HG02083.hp2 HG03471.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.295-981C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063246 | ||||||
chr1:40063323
|
A | T | 7 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(4): Show | 10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-904A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063323 | ||||||
chr1:40063357
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.295-870T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063357 | ||||||
chr1:40063499
|
G | T | 1 | a0001c0001t0004g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.295-728G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063499 | ||||||
chr1:40063561
|
G | C | 2 | a0001c0002t0013g0048a0001c0002t0013g0226 | 3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.295-666G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063561 | ||||||
chr1:40063674
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.295-553A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063674 | ||||||
chr1:40063796
|
G | A | 12 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(9): Show | 15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.295-431G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063796 | ||||||
chr1:40063817
|
G | C | 1 | a0001c0002t0015g0045 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.295-410G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063817 | ||||||
chr1:40064076
|
G | C | 2 | a0001c0001t0004g0136a0001c0001t0004g0138 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.295-151G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40064076 | ||||||
chr1:40064450
|
C | T | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439-24C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 5/12 | chr1 | 40064450 | ||||||
chr1:40064672
|
C | G | 28 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(25): Show | 55 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.524+113C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064672 | ||||||
chr1:40064786
|
G | C | 2 | a0001c0002t0013g0048a0001c0002t0013g0226 | 3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.524+227G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064786 | ||||||
chr1:40064794
|
C | G | 3 | a0001c0001t0003g0043a0001c0001t0003g0186a0001c0001t0003g0207 | 4 | NA18944.hp2 NA18999.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.524+235C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064794 | ||||||
chr1:40064880
|
A | G | 4 | a0001c0001t0005g0021a0001c0001t0005g0058a0001c0001t0005g0060others(1): Show | 5 | HG02258.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+321A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064880 | ||||||
chr1:40064935
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.524+376T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064935 | ||||||
chr1:40065038
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.524+479C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065038 | ||||||
chr1:40065142
|
A | G | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.524+583A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065142 | ||||||
chr1:40065422
|
A | G | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.525-793A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065422 | ||||||
chr1:40065451
|
T | C | 1 | a0001c0001t0003g0212 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.525-764T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065451 | ||||||
chr1:40065485
|
A | G | 7 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(4): Show | 10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.525-730A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065485 | ||||||
chr1:40065606
|
G | A | 2 | a0001c0003t0004g0139a0002c0004t0004g0039 | 3 | HG02647.hp1 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525-609G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065606 | ||||||
chr1:40065608
|
T | G | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.525-607T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065608 | ||||||
chr1:40065655
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.525-560G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065655 | ||||||
chr1:40065822
|
C | A | 12 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(9): Show | 15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.525-393C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065822 | ||||||
chr1:40065992
|
G | C | 1 | a0001c0001t0001g0032 | 2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.525-223G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065992 | ||||||
chr1:40066030
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.525-185T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066030 | ||||||
chr1:40066036
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.525-179G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066036 | ||||||
chr1:40066128
|
T | C | 1 | a0001c0001t0012g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.525-87T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066128 | ||||||
chr1:40066172
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.525-43G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066172 | ||||||
chr1:40066178
|
G | A | 6 | a0001c0001t0004g0010a0001c0001t0005g0010a0001c0001t0005g0021others(3): Show | 9 | HG02258.hp2 HG03195.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.525-37G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066178 | ||||||
chr1:40066332
|
C | A | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.630+12C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066332 | ||||||
chr1:40066356
|
C | T | 18 | a0001c0001t0004g0010a0001c0001t0004g0062a0001c0001t0005g0010others(15): Show | 27 | HG00423.hp2 HG01496.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.630+36C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066356 | ||||||
chr1:40066659
|
A | C | 1 | a0001c0002t0015g0045 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.630+339A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066659 | ||||||
chr1:40066667
|
T | C | 1 | a0001c0001t0003g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.630+347T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066667 | ||||||
chr1:40066760
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0140others(2): Show | 12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+440G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066760 | ||||||
chr1:40067307
|
A | G | 1 | a0001c0001t0003g0181 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.631-233A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40067307 | ||||||
chr1:40067386
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0134 | 2 | NA18973.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.631-154A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40067386 | ||||||
chr1:40067748
|
TACA | T | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.808+36_808+38delCA others(1): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 40067748 | |||||
chr1:40067772
|
C | G | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.808+55C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067772 | ||||||
chr1:40067826
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.808+109C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067826 | ||||||
chr1:40067827
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.808+110G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067827 | ||||||
chr1:40067948
|
T | G | 3 | a0001c0001t0011g0013a0001c0001t0011g0055a0001c0001t0023g0054 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+231T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067948 | ||||||
chr1:40068223
|
T | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.808+506T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068223 | ||||||
chr1:40068286
|
T | C | 3 | a0001c0001t0011g0013a0001c0001t0011g0055a0001c0001t0023g0054 | 5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+569T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068286 | ||||||
chr1:40068348
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.808+631G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068348 | ||||||
chr1:40068351
|
A | G | 59 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.808+634A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068351 | ||||||
chr1:40068401
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(127): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.808+684C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068401 | ||||||
chr1:40068402
|
C | T | 3 | a0001c0001t0008g0018a0001c0001t0008g0219a0001c0001t0018g0224 | 5 | NA18949.hp1 NA18993.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+685C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068402 | ||||||
chr1:40068429
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.808+712C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068429 | ||||||
chr1:40068443
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.808+726T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068443 | ||||||
chr1:40068639
|
GA | G | 7 | a0001c0001t0001g0094a0001c0001t0004g0155a0001c0002t0010g0046others(4): Show | 11 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.808+932delA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 40068639 | |||||
chr1:40068751
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.809-939G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068751 | ||||||
chr1:40068826
|
TTTTTA | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(76): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.809-849_809-845del others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 40068826 | |||||
chr1:40068973
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.809-717C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068973 | ||||||
chr1:40069063
|
A | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.809-627A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069063 | ||||||
chr1:40069170
|
T | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(30): Show | 66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.809-520T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069170 | ||||||
chr1:40069268
|
A | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0017others(40): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.809-422A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069268 | ||||||
chr1:40069322
|
G | C | 1 | a0001c0001t0003g0196 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.809-368G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069322 | ||||||
chr1:40069324
|
G | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0077 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.809-366G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069324 | ||||||
chr1:40069334
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(179): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.809-356C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069334 | ||||||
chr1:40069395
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(128): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.809-295T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069395 | ||||||
chr1:40069405
|
C | T | 2 | a0001c0001t0005g0058a0001c0001t0005g0061 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.809-285C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069405 | ||||||
chr1:40069420
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.809-270T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069420 | ||||||
chr1:40069501
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0140others(3): Show | 13 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.809-189T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069501 | ||||||
chr1:40069667
|
C | T | 6 | a0001c0001t0006g0007a0001c0001t0006g0023a0001c0001t0006g0024others(3): Show | 12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-23C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069667 | ||||||
chr1:40069949
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0119 | 6 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+75G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40069949 | ||||||
chr1:40069973
|
G | A | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0014others(29): Show | 65 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.993+99G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40069973 | ||||||
chr1:40069995
|
C | T | 1 | a0001c0001t0023g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.993+121C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40069995 | ||||||
chr1:40070003
|
G | A | 1 | a0001c0001t0014g0038 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.993+129G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40070003 | ||||||
chr1:40070071
|
T | C | 5 | a0001c0001t0002g0026a0001c0001t0002g0074a0001c0001t0002g0080others(2): Show | 6 | HG00597.hp1 NA18943.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-88T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40070071 | ||||||
chr1:40070115
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.994-44G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40070115 | ||||||
chr1:40070298
|
T | G | 5 | a0001c0001t0004g0062a0001c0001t0005g0022a0001c0001t0005g0063others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+16T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/12 | chr1 | 40070298 | ||||||
chr1:40070402
|
C | CT | 241 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(238): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1118-28_1118-27ins others(1): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/12 | chr1 | 40070402 | ||||||
chr1:40070692
|
C | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0112a0001c0001t0001g0128 | 5 | HG00408.hp1 HG00673.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-144C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 11/12 | chr1 | 40070692 | ||||||
chr1:40071130
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1344+151A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071130 | ||||||
chr1:40071242
|
G | A | 5 | a0001c0001t0004g0136a0001c0001t0004g0138a0001c0003t0004g0137others(2): Show | 6 | HG02074.hp2 HG02523.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-208G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071242 | ||||||
chr1:40071266
|
CT | C | 5 | a0001c0002t0010g0046a0001c0002t0010g0047a0001c0002t0013g0048others(2): Show | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-182delT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 40071266 | |||||
chr1:40071342
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C | T | 2 | a0001c0001t0011g0013a0001c0001t0011g0055 | 4 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-108C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071342 | ||||||
chr1:40071434
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T | C | 2 | a0001c0001t0003g0193a0001c0001t0020g0194 | 2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1345-16T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071434 |