geneid | 348807 |
---|---|
ensemblid | ENSG00000163885.12 |
hgncid | 26842 |
symbol | CFAP100 |
name | cilia and flagella associated protein 100 |
refseq_nuc | NM_182628.3 |
refseq_prot | NP_872434.2 |
ensembl_nuc | ENST00000352312.6 |
ensembl_prot | ENSP00000344749.1 |
mane_status | MANE Select |
chr | chr3 |
start | 126394909 |
end | 126436556 |
strand | + |
ver | v1.2 |
region | chr3:126394909-126436556 |
region5000 | chr3:126389909-126441556 |
regionname0 | CFAP100_chr3_126394909_126436556 |
regionname5000 | CFAP100_chr3_126389909_126441556 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 611 | 361 | 70 | 71 | 162 | 15 | 42 | 122 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0002 | 0/0 | 611 | 18 | 1 | 0 | 16 | 0 | 1 | 13 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0003 | 0/0 | 610 | 11 | 0 | 6 | 1 | 1 | 3 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0004 | 0/0 | 611 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0005 | 0/0 | 611 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0006 | 0/0 | 611 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0007 | 0/0 | 611 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0008 | 0/0 | 611 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0009 | 0/0 | 611 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0010 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0011 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0012 | 0/1 | 611 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0013 | 0/0 | 611 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0014 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0015 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0016 | 0/0 | 611 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0017 | 0/0 | 611 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0018 | 0/0 | 611 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1836 | 250 | 39 | 51 | 127 | 10 | 22 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0002 | 0/0 | 1836 | 65 | 6 | 16 | 19 | 5 | 19 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0003 | 0/0 | 1836 | 25 | 22 | 3 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0004 | 0/0 | 1836 | 18 | 1 | 0 | 16 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0005 | 0/0 | 1833 | 11 | 0 | 6 | 1 | 1 | 3 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0006 | 0/0 | 1836 | 10 | 0 | 0 | 10 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0007 | 0/0 | 1836 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0008 | 0/0 | 1836 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0009 | 0/0 | 1836 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0010 | 0/0 | 1836 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0011 | 0/0 | 1836 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0012 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0013 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0014 | 0/0 | 1836 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0015 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0016 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0017 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0018 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0019 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0020 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0021 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0022 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0023 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0024 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0025 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0026 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0027 | 0/1 | 1836 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0028 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
c0029 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 282 | 405 | 86 | 76 | 182 | 14 | 45 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
t0002 | 0/0 | 282 | 14 | 8 | 3 | 0 | 2 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
t0003 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
t0004 | 0/0 | 282 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
t0005 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0392 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1836 | 250 | 39 | 51 | 127 | 10 | 22 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0002 | 0/0 | 1836 | 65 | 6 | 16 | 19 | 5 | 19 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0003 | 0/0 | 1836 | 25 | 22 | 3 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0006 | 0/0 | 1836 | 10 | 0 | 0 | 10 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0008 | 0/0 | 1836 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0013 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0016 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0018 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0023 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0025 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0002c0004 | 0/0 | 1836 | 18 | 1 | 0 | 16 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0003c0005 | 0/0 | 1833 | 11 | 0 | 6 | 1 | 1 | 3 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0004c0007 | 0/0 | 1836 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0004c0028 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0005c0009 | 0/0 | 1836 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0005c0024 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0006c0011 | 0/0 | 1836 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0007c0010 | 0/0 | 1836 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0008c0014 | 0/0 | 1836 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0009c0012 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0010c0029 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0011c0017 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0012c0027 | 0/1 | 1836 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0013c0022 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0014c0020 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0015c0021 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0016c0026 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0017c0019 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0018c0015 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2117 | 241 | 36 | 50 | 125 | 8 | 21 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0001t0002 | 0/0 | 2117 | 7 | 3 | 1 | 0 | 2 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0001t0003 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0001t0005 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0002t0001 | 0/0 | 2117 | 63 | 6 | 14 | 19 | 5 | 19 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0002t0002 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0002t0004 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0003t0001 | 0/0 | 2117 | 25 | 22 | 3 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0006t0001 | 0/0 | 2117 | 10 | 0 | 0 | 10 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0008t0001 | 0/0 | 2117 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0013t0001 | 0/0 | 2117 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0016t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0018t0001 | 0/0 | 2117 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0023t0001 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0001c0025t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0002c0004t0001 | 0/0 | 2117 | 18 | 1 | 0 | 16 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0003c0005t0001 | 0/0 | 2114 | 11 | 0 | 6 | 1 | 1 | 3 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0004c0007t0001 | 0/0 | 2117 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0004c0028t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0005c0009t0001 | 0/0 | 2117 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0005c0009t0002 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0005c0024t0002 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0006c0011t0002 | 0/0 | 2117 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0007c0010t0001 | 0/0 | 2117 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0008c0014t0001 | 0/0 | 2117 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0009c0012t0001 | 0/0 | 2117 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0010c0029t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0011c0017t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0012c0027t0001 | 0/1 | 2117 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0013c0022t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0014c0020t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0015c0021t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0016c0026t0002 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0017c0019t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
a0018c0015t0001 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | copy fasta | chr3 | 126389909 | 126441556 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0001g0392 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0002t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0008t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0013t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0016t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0018t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0023t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0001c0025t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0002c0004t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0003c0005t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0007t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0004c0028t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0009t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0005c0024t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0006c0011t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0006c0011t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0006c0011t0002g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0007c0010t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0007c0010t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0007c0010t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0008c0014t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0008c0014t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0009c0012t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0009c0012t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0010c0029t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0011c0017t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0012c0027t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0013c0022t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0014c0020t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0015c0021t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0016c0026t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0017c0019t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
a0018c0015t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0357 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00140 | hp1 | a0003 | c0005 | t0001 | g0012 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | GBR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0071 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0033 | EUR | FIN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00408 | hp2 | a0008 | c0014 | t0001 | g0257 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00544 | hp1 | a0002 | c0004 | t0001 | g0213 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00639 | hp1 | a0003 | c0005 | t0001 | g0240 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00733 | hp1 | a0007 | c0010 | t0001 | g0287 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01099 | hp1 | a0003 | c0005 | t0001 | g0167 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01106 | hp1 | a0003 | c0005 | t0001 | g0186 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01109 | hp1 | a0007 | c0010 | t0001 | g0187 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01243 | hp1 | a0003 | c0005 | t0001 | g0075 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0375 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01257 | hp2 | a0003 | c0005 | t0001 | g0166 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01258 | hp2 | a0003 | c0005 | t0001 | g0012 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01358 | hp2 | a0016 | c0026 | t0002 | g0250 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01361 | hp2 | a0001 | c0002 | t0004 | g0024 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0376 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01891 | hp1 | a0009 | c0012 | t0001 | g0055 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0380 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01993 | hp1 | a0001 | c0023 | t0001 | g0170 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0388 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0386 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02055 | hp2 | a0004 | c0007 | t0001 | g0126 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02080 | hp2 | a0002 | c0004 | t0001 | g0183 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02132 | hp1 | a0002 | c0004 | t0001 | g0227 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02145 | hp2 | a0005 | c0009 | t0001 | g0145 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0232 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02280 | hp1 | a0005 | c0009 | t0002 | g0043 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02280 | hp2 | a0005 | c0009 | t0001 | g0029 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0387 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02451 | hp2 | a0010 | c0029 | t0001 | g0065 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0391 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02622 | hp1 | a0009 | c0012 | t0001 | g0026 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0268 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0374 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0373 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02698 | hp2 | a0001 | c0018 | t0001 | g0305 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02738 | hp1 | a0003 | c0005 | t0001 | g0149 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0131 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02886 | hp2 | a0006 | c0011 | t0002 | g0168 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02895 | hp1 | a0001 | c0013 | t0001 | g0010 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02895 | hp2 | a0004 | c0007 | t0001 | g0139 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02896 | hp2 | a0014 | c0020 | t0001 | g0078 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02897 | hp2 | a0001 | c0013 | t0001 | g0010 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02922 | hp2 | a0005 | c0009 | t0001 | g0280 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02965 | hp1 | a0006 | c0011 | t0002 | g0239 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02976 | hp2 | a0001 | c0025 | t0001 | g0044 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03041 | hp1 | a0015 | c0021 | t0001 | g0056 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03098 | hp1 | a0005 | c0009 | t0001 | g0205 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03139 | hp1 | a0011 | c0017 | t0001 | g0144 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03209 | hp2 | a0006 | c0011 | t0002 | g0393 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03239 | hp2 | a0003 | c0005 | t0001 | g0164 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03453 | hp2 | a0004 | c0007 | t0001 | g0142 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03579 | hp1 | a0007 | c0010 | t0001 | g0190 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0390 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03688 | hp1 | a0003 | c0005 | t0001 | g0163 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0331 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0392 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03927 | hp2 | a0002 | c0004 | t0001 | g0218 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0370 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0350 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | BEB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | STU | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18944 | hp2 | a0001 | c0008 | t0001 | g0099 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18945 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18951 | hp2 | a0002 | c0004 | t0001 | g0217 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18957 | hp1 | a0002 | c0004 | t0001 | g0223 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18965 | hp1 | a0002 | c0004 | t0001 | g0381 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18967 | hp1 | a0001 | c0006 | t0001 | g0279 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18967 | hp2 | a0001 | c0016 | t0001 | g0255 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18968 | hp1 | a0003 | c0005 | t0001 | g0353 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0319 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18974 | hp1 | a0001 | c0008 | t0001 | g0092 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18977 | hp2 | a0001 | c0006 | t0001 | g0277 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18979 | hp2 | a0001 | c0008 | t0001 | g0100 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18980 | hp2 | a0002 | c0004 | t0001 | g0184 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18981 | hp1 | a0008 | c0014 | t0001 | g0066 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18987 | hp2 | a0018 | c0015 | t0001 | g0385 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18990 | hp1 | a0002 | c0004 | t0001 | g0228 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18995 | hp2 | a0002 | c0004 | t0001 | g0221 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18999 | hp2 | a0001 | c0006 | t0001 | g0016 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19000 | hp2 | a0002 | c0004 | t0001 | g0229 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19001 | hp1 | a0002 | c0004 | t0001 | g0382 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19001 | hp2 | a0001 | c0006 | t0001 | g0278 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19002 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19011 | hp2 | a0002 | c0004 | t0001 | g0230 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19012 | hp2 | a0001 | c0008 | t0001 | g0007 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19043 | hp1 | a0005 | c0024 | t0002 | g0200 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19058 | hp1 | a0002 | c0004 | t0001 | g0224 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0372 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19060 | hp1 | a0013 | c0022 | t0001 | g0101 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19063 | hp1 | a0001 | c0006 | t0001 | g0016 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19065 | hp2 | a0001 | c0006 | t0001 | g0276 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19066 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19076 | hp2 | a0001 | c0008 | t0001 | g0007 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19079 | hp2 | a0002 | c0004 | t0001 | g0220 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19081 | hp1 | a0017 | c0019 | t0001 | g0169 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19091 | hp2 | a0002 | c0004 | t0001 | g0089 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | ASW | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0246 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0310 | EUR | TSI | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | GIH | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0383 | SAS | GIH | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02109 | hp1 | a0004 | c0007 | t0001 | g0045 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02109 | hp2 | a0004 | c0007 | t0001 | g0141 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03471 | hp1 | a0004 | c0007 | t0001 | g0267 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA18955 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0146 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
NA21309 | hp2 | a0004 | c0028 | t0001 | g0140 | AFR | LWK | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
homoSapiens_chm13v2 | hp1 | a0012 | c0027 | t0001 | g0063 | REF | REF | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | CFAP100_chr3_126389909_126441556 | CFAP100 | chr3 | 126389909 | 126441556 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126396014
|
C | A | 1 | a0018 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.14C>A | p.Pro5Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/17 | 143/2117 | 14/1836 | 5/611 | chr3 | 126396014 | ||
chr3:126396014
|
C | T | 1 | a0010 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.14C>T | p.Pro5Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/17 | 143/2117 | 14/1836 | 5/611 | chr3 | 126396014 | ||
chr3:126414156
|
C | A | 1 | a0002 | 18 | HG00544.hp1 HG02080.hp2 HG02132.hp1 others(15): Show |
missense_variant | MODERATE | c.202C>A | p.Gln68Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/17 | 331/2117 | 202/1836 | 68/611 | chr3 | 126414156 | ||
chr3:126416454
|
G | A | 1 | a0017 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.364G>A | p.Glu122Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/17 | 493/2117 | 364/1836 | 122/611 | chr3 | 126416454 | ||
chr3:126418717
|
C | G | 1 | a0004 | 7 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
missense_variant | MODERATE | c.593C>G | p.Ala198Gly | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 722/2117 | 593/1836 | 198/611 | chr3 | 126418717 | ||
chr3:126419122
|
C | T | 1 | a0016 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.697C>T | p.Arg233Trp | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/17 | 826/2117 | 697/1836 | 233/611 | chr3 | 126419122 | ||
chr3:126419123
|
G | A | 1 | a0011 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.698G>A | p.Arg233Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/17 | 827/2117 | 698/1836 | 233/611 | chr3 | 126419123 | ||
chr3:126420106
|
G | A | 1 | a0006 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.959G>A | p.Gly320Asp | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1088/2117 | 959/1836 | 320/611 | chr3 | 126420106 | ||
chr3:126420145
|
T | C | 2 | a0009a0015 | 3 | HG01891.hp1 HG02622.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.998T>C | p.Met333Thr | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1127/2117 | 998/1836 | 333/611 | chr3 | 126420145 | ||
chr3:126420157
|
G | A | 1 | a0007 | 3 | HG00733.hp1 HG01109.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1010G>A | p.Arg337Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1139/2117 | 1010/1836 | 337/611 | chr3 | 126420157 | ||
chr3:126420181
|
C | T | 1 | a0005 | 6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
missense_variant | MODERATE | c.1034C>T | p.Pro345Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/17 | 1163/2117 | 1034/1836 | 345/611 | chr3 | 126420181 | ||
chr3:126423348
|
C | T | 1 | a0012 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1106C>T | p.Thr369Met | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 12/17 | 1235/2117 | 1106/1836 | 369/611 | chr3 | 126423348 | ||
chr3:126423590
|
CGGA | C | 1 | a0003 | 11 | HG00140.hp1 HG00639.hp1 HG01099.hp1 others(8): Show |
conservative_inframe_deletion | MODERATE | c.1234_1236delGAG | p.Glu412del | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/17 | 1363/2117 | 1234/1836 | 412/611 | INFO_REALIGN_3_PRIME | chr3 | 126423590 | |
chr3:126423636
|
G | T | 1 | a0008 | 2 | HG00408.hp2 NA18981.hp1 |
missense_variant | MODERATE | c.1278G>T | p.Gln426His | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/17 | 1407/2117 | 1278/1836 | 426/611 | chr3 | 126423636 | ||
chr3:126433184
|
G | A | 1 | a0014 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1402G>A | p.Glu468Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/17 | 1531/2117 | 1402/1836 | 468/611 | chr3 | 126433184 | ||
chr3:126434222
|
G | A | 1 | a0013 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1469G>A | p.Arg490Gln | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/17 | 1598/2117 | 1469/1836 | 490/611 | chr3 | 126434222 | ||
chr3:126436375
|
G | A | 1 | a0015 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1807G>A | p.Glu603Lys | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 17/17 | 1936/2117 | 1807/1836 | 603/611 | chr3 | 126436375 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126396015
|
G | A | 2 | a0001c0006a0001c0016 | 11 | NA18945.hp1 NA18955.hp2 NA18967.hp1 others(8): Show |
synonymous_variant | LOW | c.15G>A | p.Pro5Pro | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/17 | 144/2117 | 15/1836 | 5/611 | chr3 | 126396015 | ||
chr3:126416340
|
C | A | 1 | a0011c0017 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.250C>A | p.Arg84Arg | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/17 | 379/2117 | 250/1836 | 84/611 | chr3 | 126416340 | ||
chr3:126416366
|
C | A | 1 | a0001c0018 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.276C>A | p.Ser92Ser | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/17 | 405/2117 | 276/1836 | 92/611 | chr3 | 126416366 | ||
chr3:126418613
|
T | C | 2 | a0001c0003a0014c0020 | 26 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(23): Show |
splice_region_variant&synonymous_variant | LOW | c.489T>C | p.Tyr163Tyr | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 618/2117 | 489/1836 | 163/611 | chr3 | 126418613 | ||
chr3:126418715
|
C | T | 9 | a0001c0002a0001c0003a0001c0016others(6): Show | 105 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
synonymous_variant | LOW | c.591C>T | p.Ala197Ala | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 720/2117 | 591/1836 | 197/611 | chr3 | 126418715 | ||
chr3:126418733
|
C | T | 1 | a0001c0013 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.609C>T | p.Phe203Phe | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/17 | 738/2117 | 609/1836 | 203/611 | chr3 | 126418733 | ||
chr3:126419694
|
A | C | 1 | a0001c0025 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.789A>C | p.Leu263Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 9/17 | 918/2117 | 789/1836 | 263/611 | chr3 | 126419694 | ||
chr3:126423567
|
G | A | 1 | a0004c0028 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1209G>A | p.Ser403Ser | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/17 | 1338/2117 | 1209/1836 | 403/611 | chr3 | 126423567 | ||
chr3:126433138
|
C | T | 1 | a0001c0023 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1356C>T | p.Asp452Asp | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/17 | 1485/2117 | 1356/1836 | 452/611 | chr3 | 126433138 | ||
chr3:126434259
|
C | T | 1 | a0005c0024 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1506C>T | p.Gly502Gly | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/17 | 1635/2117 | 1506/1836 | 502/611 | chr3 | 126434259 | ||
chr3:126434307
|
A | G | 2 | a0001c0008a0013c0022 | 6 | NA18944.hp2 NA18974.hp1 NA18979.hp2 others(3): Show |
synonymous_variant | LOW | c.1554A>G | p.Leu518Leu | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/17 | 1683/2117 | 1554/1836 | 518/611 | chr3 | 126434307 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126394928
|
C | G | 1 | a0001c0001t0005 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/17 | 1073 | chr3 | 126394928 | |||||
chr3:126394958
|
G | C | 1 | a0001c0001t0003 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/17 | 1043 | chr3 | 126394958 | |||||
chr3:126394959
|
A | G | 1 | a0001c0002t0004 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/17 | 1042 | chr3 | 126394959 | |||||
chr3:126436482
|
C | T | 6 | a0001c0001t0002a0001c0002t0002a0005c0009t0002others(3): Show | 14 | HG01099.hp2 HG01358.hp2 HG01981.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*78C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 17/17 | 78 | chr3 | 126436482 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126395010
|
C | A | 1 | a0001c0001t0001g0004 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-60+32C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395010 | ||||||
chr3:126395039
|
C | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0027others(11): Show | 15 | HG00323.hp2 HG00733.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-60+61C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395039 | ||||||
chr3:126395039
|
C | T | 1 | a0006c0011t0002g0393 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-60+61C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395039 | ||||||
chr3:126395042
|
C | T | 2 | a0001c0002t0001g0391a0001c0002t0001g0392 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-60+64C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395042 | ||||||
chr3:126395099
|
A | G | 1 | a0001c0002t0001g0390 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-60+121A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395099 | ||||||
chr3:126395252
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-60+274G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395252 | ||||||
chr3:126395399
|
A | G | 1 | a0001c0001t0001g0389 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-60+421A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395399 | ||||||
chr3:126395613
|
G | T | 6 | a0001c0001t0001g0386a0001c0002t0001g0023a0001c0002t0001g0024others(3): Show | 7 | HG01361.hp2 HG01928.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-59-329G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395613 | ||||||
chr3:126395803
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG02886.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-59-139T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395803 | ||||||
chr3:126395864
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-59-78G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 1/16 | chr3 | 126395864 | ||||||
chr3:126396058
|
C | T | 1 | a0001c0002t0001g0022 | 2 | HG02132.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.49+9C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396058 | ||||||
chr3:126396092
|
A | G | 1 | a0018c0015t0001g0385 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.49+43A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396092 | ||||||
chr3:126396099
|
G | A | 2 | a0001c0001t0001g0025a0005c0009t0002g0043 | 2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.49+50G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396099 | ||||||
chr3:126396277
|
G | C | 2 | a0001c0025t0001g0044a0004c0007t0001g0045 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.49+228G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396277 | ||||||
chr3:126396313
|
G | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(170): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.49+264G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396313 | ||||||
chr3:126396511
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01261.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.49+462G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396511 | ||||||
chr3:126396522
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49+473C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396522 | ||||||
chr3:126396565
|
C | G | 1 | a0001c0003t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+516C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396565 | ||||||
chr3:126396569
|
A | G | 1 | a0001c0001t0001g0384 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.49+520A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396569 | ||||||
chr3:126396647
|
A | C | 1 | a0001c0002t0001g0392 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.49+598A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396647 | ||||||
chr3:126396661
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.49+612G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396661 | ||||||
chr3:126396773
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.49+724G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396773 | ||||||
chr3:126396805
|
C | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0237others(3): Show | 6 | HG00738.hp2 HG01168.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+756C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396805 | ||||||
chr3:126396827
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.49+778G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396827 | ||||||
chr3:126396875
|
T | A | 1 | a0006c0011t0002g0239 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49+826T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396875 | ||||||
chr3:126396905
|
A | T | 1 | a0001c0002t0001g0383 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.49+856A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396905 | ||||||
chr3:126396940
|
C | T | 23 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215others(20): Show | 23 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.49+891C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126396940 | ||||||
chr3:126397052
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.49+1003T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397052 | ||||||
chr3:126397290
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.49+1241T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397290 | ||||||
chr3:126397336
|
C | T | 15 | a0001c0001t0001g0038a0001c0001t0001g0197a0001c0001t0001g0199others(12): Show | 15 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+1287C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397336 | ||||||
chr3:126397345
|
G | A | 14 | a0001c0001t0001g0038a0001c0001t0001g0197a0001c0001t0001g0199others(11): Show | 14 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1296G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397345 | ||||||
chr3:126397348
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.49+1299C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397348 | ||||||
chr3:126397349
|
T | C | 20 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0197others(17): Show | 20 | HG01109.hp2 HG01891.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.49+1300T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397349 | ||||||
chr3:126397567
|
C | A | 29 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.49+1518C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397567 | ||||||
chr3:126397590
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.49+1541G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397590 | ||||||
chr3:126397744
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49+1695G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397744 | ||||||
chr3:126397867
|
C | T | 1 | a0004c0007t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+1818C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397867 | ||||||
chr3:126397891
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.49+1842G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397891 | ||||||
chr3:126397961
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+1912G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126397961 | ||||||
chr3:126398268
|
G | A | 1 | a0004c0007t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+2219G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398268 | ||||||
chr3:126398288
|
G | A | 1 | a0004c0007t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+2239G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398288 | ||||||
chr3:126398307
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+2258G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398307 | ||||||
chr3:126398312
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+2263C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398312 | ||||||
chr3:126398316
|
T | C | 12 | a0001c0001t0001g0077a0001c0001t0002g0248a0001c0001t0002g0249others(9): Show | 12 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+2267T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398316 | ||||||
chr3:126398429
|
A | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(333): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.49+2380A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398429 | ||||||
chr3:126398459
|
C | A | 11 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG00741.hp2 HG02083.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+2410C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398459 | ||||||
chr3:126398593
|
T | C | 2 | a0001c0003t0001g0003a0004c0007t0001g0045 | 4 | HG01255.hp2 HG02109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+2544T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398593 | ||||||
chr3:126398697
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.49+2648C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398697 | ||||||
chr3:126398717
|
A | T | 1 | a0001c0001t0001g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.49+2668A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398717 | ||||||
chr3:126398827
|
G | A | 2 | a0004c0007t0001g0126a0004c0007t0001g0267 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+2778G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398827 | ||||||
chr3:126398879
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+2830G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398879 | ||||||
chr3:126398907
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.49+2858C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398907 | ||||||
chr3:126398923
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.49+2874A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126398923 | ||||||
chr3:126399120
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+3071C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399120 | ||||||
chr3:126399160
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0209a0001c0003t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3111C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399160 | ||||||
chr3:126399274
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49+3225G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399274 | ||||||
chr3:126399453
|
A | G | 30 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(27): Show | 30 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+3404A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399453 | ||||||
chr3:126399718
|
A | G | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0251others(3): Show | 6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+3669A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399718 | ||||||
chr3:126399885
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0389 | 2 | NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.49+3836G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399885 | ||||||
chr3:126399885
|
G | C | 1 | a0001c0003t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+3836G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399885 | ||||||
chr3:126399946
|
G | C | 14 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(11): Show | 19 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.49+3897G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399946 | ||||||
chr3:126399978
|
G | A | 1 | a0004c0007t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+3929G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126399978 | ||||||
chr3:126400027
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49+3978C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400027 | ||||||
chr3:126400062
|
C | T | 1 | a0004c0007t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+4013C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400062 | ||||||
chr3:126400091
|
T | C | 14 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0234others(11): Show | 15 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+4042T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400091 | ||||||
chr3:126400126
|
A | G | 1 | a0001c0001t0001g0377 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.49+4077A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400126 | ||||||
chr3:126400460
|
A | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0199a0001c0001t0001g0201others(8): Show | 11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+4411A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400460 | ||||||
chr3:126400525
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.49+4476G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400525 | ||||||
chr3:126400529
|
G | A | 6 | a0004c0007t0001g0126a0004c0007t0001g0139a0004c0007t0001g0141others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4480G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400529 | ||||||
chr3:126400549
|
T | C | 34 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0052others(31): Show | 42 | HG00738.hp2 HG01081.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.49+4500T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400549 | ||||||
chr3:126400549
|
T | G | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0007c0010t0001g0287others(3): Show | 6 | HG00733.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4500T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400549 | ||||||
chr3:126400568
|
A | G | 2 | a0001c0002t0001g0271a0001c0002t0001g0272 | 2 | NA18947.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.49+4519A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400568 | ||||||
chr3:126400569
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.49+4520T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400569 | ||||||
chr3:126400604
|
T | C | 3 | a0001c0001t0001g0077a0001c0003t0001g0076a0001c0003t0001g0232 | 3 | HG01243.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.49+4555T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400604 | ||||||
chr3:126400606
|
A | G | 150 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0017others(147): Show | 162 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.49+4557A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400606 | ||||||
chr3:126400620
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.49+4571C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400620 | ||||||
chr3:126400646
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.49+4597G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400646 | ||||||
chr3:126400668
|
C | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0243 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.49+4619C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400668 | ||||||
chr3:126400709
|
G | A | 1 | a0003c0005t0001g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.49+4660G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400709 | ||||||
chr3:126400717
|
A | T | 13 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0001t0001g0354others(10): Show | 15 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+4668A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400717 | ||||||
chr3:126400751
|
C | CA | 19 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0165others(16): Show | 22 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.49+4712dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126400751 | |||||
chr3:126400788
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0051a0001c0001t0001g0052others(7): Show | 11 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+4739C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400788 | ||||||
chr3:126400855
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49+4806C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400855 | ||||||
chr3:126400855
|
C | T | 4 | a0001c0002t0001g0192a0001c0002t0001g0376a0001c0002t0001g0390others(1): Show | 4 | HG01099.hp2 HG01433.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+4806C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400855 | ||||||
chr3:126400910
|
A | G | 11 | a0001c0001t0001g0038a0001c0001t0001g0199a0001c0001t0001g0201others(8): Show | 11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+4861A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400910 | ||||||
chr3:126400942
|
C | A | 22 | a0001c0001t0001g0072a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 27 | HG00323.hp1 HG00741.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+4893C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126400942 | ||||||
chr3:126401005
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.49+4956C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401005 | ||||||
chr3:126401039
|
A | G | 1 | a0001c0013t0001g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+4990A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401039 | ||||||
chr3:126401070
|
A | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0199a0001c0001t0001g0201others(8): Show | 11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+5021A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401070 | ||||||
chr3:126401091
|
C | A | 1 | a0001c0001t0001g0289 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.49+5042C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401091 | ||||||
chr3:126401104
|
A | C | 1 | a0001c0002t0001g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.49+5055A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401104 | ||||||
chr3:126401170
|
G | A | 1 | a0001c0002t0001g0359 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.49+5121G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401170 | ||||||
chr3:126401209
|
G | A | 323 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(320): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.49+5160G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401209 | ||||||
chr3:126401227
|
A | G | 393 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(390): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.49+5178A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401227 | ||||||
chr3:126401360
|
A | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0274others(25): Show | 35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.49+5311A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401360 | ||||||
chr3:126401394
|
A | ATT | 15 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0157others(12): Show | 16 | HG00140.hp2 HG00673.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+5348_49+5349dup others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401394 | |||||
chr3:126401396
|
TTTATATA others(8): Show |
T | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.49+5349_49+5363del others(15): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401396 | |||||
chr3:126401397
|
T | TTA | 36 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0067others(33): Show | 37 | HG00558.hp2 HG00741.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+5393_49+5394dup others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTATA | 29 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0046others(26): Show | 30 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.49+5391_49+5394dup others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTATATA | 10 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0116others(7): Show | 11 | HG00408.hp2 HG00597.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+5389_49+5394dup others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTATATAT others(1): Show |
9 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0001g0080others(6): Show | 9 | HG01168.hp1 HG01261.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5387_49+5394dup others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0118a0001c0001t0001g0352a0001c0002t0001g0050others(1): Show | 4 | HG02886.hp2 NA18988.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5385_49+5394dup others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.49+5383_49+5394dup others(12): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTA | 32 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0040others(29): Show | 34 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATA | 25 | a0001c0001t0001g0013a0001c0001t0001g0121a0001c0001t0001g0122others(22): Show | 26 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATAT others(1): Show |
13 | a0001c0001t0001g0041a0001c0001t0001g0060a0001c0001t0001g0253others(10): Show | 13 | HG00408.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATAT others(3): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0289a0001c0001t0001g0333others(2): Show | 5 | HG00099.hp1 NA18963.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+5349_49+5350ins others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATAT others(5): Show |
1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(12): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATAT others(9): Show |
1 | a0001c0001t0001g0336 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(16): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATAT others(11): Show |
1 | a0002c0004t0001g0382 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(18): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
T | TTTTATAT others(19): Show |
1 | a0001c0001t0001g0160 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.49+5349_49+5350ins others(26): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTA | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0039others(28): Show | 32 | HG00280.hp1 HG00544.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.49+5393_49+5394del others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATA | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0084a0001c0001t0001g0085others(11): Show | 15 | HG01106.hp1 HG01243.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+5391_49+5394del others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATA | T | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0346others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+5389_49+5394del others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(1): Show |
T | 3 | a0001c0002t0001g0073a0004c0007t0001g0139a0004c0028t0001g0140 | 3 | HG02895.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.49+5387_49+5394del others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(3): Show |
T | 4 | a0001c0001t0001g0052a0001c0001t0001g0185a0001c0002t0001g0083others(1): Show | 4 | HG00738.hp2 HG01175.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5385_49+5394del others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(5): Show |
T | 10 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0197others(7): Show | 12 | HG00323.hp2 HG01070.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+5383_49+5394del others(12): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(7): Show |
T | 4 | a0001c0001t0001g0191a0001c0002t0001g0374a0001c0002t0001g0383others(1): Show | 4 | HG01099.hp2 HG02683.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5381_49+5394del others(14): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(9): Show |
T | 10 | a0001c0001t0001g0182a0001c0001t0001g0371a0001c0002t0001g0192others(7): Show | 10 | HG01433.hp1 HG02080.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+5379_49+5394del others(16): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(11): Show |
T | 39 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(36): Show | 41 | HG00735.hp1 HG01074.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.49+5377_49+5394del others(18): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(13): Show |
T | 5 | a0001c0001t0001g0171a0001c0001t0001g0360a0001c0001t0001g0361others(2): Show | 5 | HG01993.hp1 HG01993.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+5375_49+5394del others(20): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(17): Show |
T | 2 | a0001c0001t0001g0244a0001c0002t0001g0032 | 2 | HG00597.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.49+5371_49+5394del others(24): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(19): Show |
T | 27 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0274others(24): Show | 34 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.49+5369_49+5394del others(26): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(21): Show |
T | 14 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0337others(11): Show | 14 | HG00609.hp1 HG02040.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+5367_49+5394del others(28): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401397
|
TTATATAT others(33): Show |
T | 2 | a0001c0001t0001g0209a0014c0020t0001g0078 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.49+5355_49+5394del others(40): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126401397 | |||||
chr3:126401398
|
TATATATA others(22): Show |
T | 1 | a0001c0001t0001g0288 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.49+5350_49+5378del others(29): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401398 | ||||||
chr3:126401399
|
A | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0123others(8): Show | 13 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+5350A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401399 | ||||||
chr3:126401401
|
A | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0156others(5): Show | 9 | HG00544.hp1 HG02071.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5352A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401401 | ||||||
chr3:126401403
|
A | T | 1 | a0001c0001t0001g0299 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.49+5354A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401403 | ||||||
chr3:126401405
|
A | T | 1 | a0003c0005t0001g0353 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.49+5356A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401405 | ||||||
chr3:126401407
|
A | T | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+5358A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401407 | ||||||
chr3:126401411
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.49+5362A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401411 | ||||||
chr3:126401417
|
A | T | 1 | a0003c0005t0001g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.49+5368A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401417 | ||||||
chr3:126401423
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49+5374A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401423 | ||||||
chr3:126401427
|
A | T | 12 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0337others(9): Show | 12 | HG00609.hp1 HG02040.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+5378A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401427 | ||||||
chr3:126401429
|
A | T | 13 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0288others(10): Show | 13 | HG00609.hp1 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+5380A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401429 | ||||||
chr3:126401476
|
T | C | 2 | a0004c0007t0001g0126a0004c0007t0001g0267 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+5427T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401476 | ||||||
chr3:126401511
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49+5462A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401511 | ||||||
chr3:126401516
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0009c0012t0001g0026others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+5467C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401516 | ||||||
chr3:126401589
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+5540A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401589 | ||||||
chr3:126401691
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0251others(3): Show | 6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-5481G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401691 | ||||||
chr3:126401701
|
A | G | 317 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(314): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.50-5471A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401701 | ||||||
chr3:126401757
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.50-5415G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401757 | ||||||
chr3:126401806
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-5366G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401806 | ||||||
chr3:126401811
|
T | C | 2 | a0001c0001t0001g0362a0001c0001t0001g0371 | 2 | NA18964.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.50-5361T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401811 | ||||||
chr3:126401901
|
C | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(119): Show | 127 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.50-5271C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401901 | ||||||
chr3:126401957
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.50-5215C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126401957 | ||||||
chr3:126402144
|
G | A | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0002t0001g0073others(3): Show | 6 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-5028G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402144 | ||||||
chr3:126402170
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.50-5002G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402170 | ||||||
chr3:126402362
|
G | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG00733.hp2 HG01071.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-4810G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402362 | ||||||
chr3:126402370
|
G | A | 2 | a0001c0001t0001g0209a0014c0020t0001g0078 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.50-4802G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402370 | ||||||
chr3:126402373
|
G | A | 1 | a0001c0002t0001g0387 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.50-4799G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402373 | ||||||
chr3:126402550
|
G | A | 1 | a0014c0020t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50-4622G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402550 | ||||||
chr3:126402694
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0251others(3): Show | 6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-4478G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402694 | ||||||
chr3:126402783
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.50-4389C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402783 | ||||||
chr3:126402827
|
G | A | 10 | a0001c0003t0001g0001a0001c0003t0001g0009a0001c0003t0001g0015others(7): Show | 15 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-4345G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402827 | ||||||
chr3:126402949
|
C | T | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | HG01081.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.50-4223C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126402949 | ||||||
chr3:126403080
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.50-4092G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403080 | ||||||
chr3:126403128
|
T | C | 6 | a0004c0007t0001g0126a0004c0007t0001g0139a0004c0007t0001g0141others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-4044T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403128 | ||||||
chr3:126403150
|
C | T | 1 | a0007c0010t0001g0287 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.50-4022C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403150 | ||||||
chr3:126403187
|
A | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0199a0001c0001t0001g0201others(8): Show | 11 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-3985A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403187 | ||||||
chr3:126403209
|
C | T | 2 | a0001c0001t0001g0209a0014c0020t0001g0078 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.50-3963C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403209 | ||||||
chr3:126403210
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0053a0001c0001t0001g0299others(1): Show | 5 | NA18998.hp2 NA19009.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-3962G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403210 | ||||||
chr3:126403267
|
C | T | 1 | a0015c0021t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.50-3905C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403267 | ||||||
chr3:126403268
|
G | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0270others(4): Show | 8 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-3904G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403268 | ||||||
chr3:126403318
|
C | T | 30 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(27): Show | 31 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.50-3854C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403318 | ||||||
chr3:126403319
|
G | C | 1 | a0001c0001t0002g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.50-3853G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403319 | ||||||
chr3:126403383
|
C | CT | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0042others(21): Show | 25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-3770dupT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | |||||
chr3:126403383
|
C | CTT | 15 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0077others(12): Show | 17 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-3771_50-3770dup others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | |||||
chr3:126403383
|
CT | C | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(185): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.50-3770delT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | |||||
chr3:126403383
|
CTT | C | 10 | a0001c0001t0001g0195a0001c0001t0001g0209a0001c0001t0001g0301others(7): Show | 10 | HG01981.hp1 HG02451.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-3771_50-3770del others(2): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126403383 | |||||
chr3:126403453
|
C | T | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(206): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.50-3719C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403453 | ||||||
chr3:126403470
|
C | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(217): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.50-3702C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403470 | ||||||
chr3:126403646
|
G | A | 1 | a0001c0001t0001g0384 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.50-3526G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403646 | ||||||
chr3:126403700
|
T | C | 1 | a0001c0001t0001g0363 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-3472T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403700 | ||||||
chr3:126403730
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.50-3442T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403730 | ||||||
chr3:126403789
|
T | C | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50-3383T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403789 | ||||||
chr3:126403829
|
C | A | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(256): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.50-3343C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403829 | ||||||
chr3:126403847
|
A | G | 1 | a0010c0029t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.50-3325A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126403847 | ||||||
chr3:126404022
|
G | C | 1 | a0005c0009t0002g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-3150G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404022 | ||||||
chr3:126404041
|
C | G | 1 | a0001c0003t0001g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-3131C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404041 | ||||||
chr3:126404042
|
G | A | 2 | a0001c0001t0001g0209a0014c0020t0001g0078 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.50-3130G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404042 | ||||||
chr3:126404106
|
G | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0274others(25): Show | 35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.50-3066G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404106 | ||||||
chr3:126404133
|
C | T | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0251others(3): Show | 6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-3039C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404133 | ||||||
chr3:126404278
|
G | C | 2 | a0001c0001t0001g0219a0002c0004t0001g0218 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.50-2894G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404278 | ||||||
chr3:126404389
|
T | C | 1 | a0003c0005t0001g0186 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.50-2783T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404389 | ||||||
chr3:126404431
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.50-2741A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404431 | ||||||
chr3:126404654
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.50-2518C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404654 | ||||||
chr3:126404754
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG00733.hp2 HG01071.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-2418A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404754 | ||||||
chr3:126404832
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0067others(47): Show | 58 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.50-2340G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404832 | ||||||
chr3:126404877
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50-2295G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404877 | ||||||
chr3:126404964
|
C | T | 8 | a0001c0001t0001g0072a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-2208C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404964 | ||||||
chr3:126404966
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-2206G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126404966 | ||||||
chr3:126405085
|
GACC | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0274others(25): Show | 35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.50-2079_50-2077del others(3): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126405085 | |||||
chr3:126405122
|
A | G | 55 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(52): Show | 57 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-2050A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405122 | ||||||
chr3:126405298
|
C | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0289a0001c0001t0001g0317others(4): Show | 8 | HG02071.hp2 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1874C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405298 | ||||||
chr3:126405419
|
T | C | 1 | a0001c0001t0001g0352 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.50-1753T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405419 | ||||||
chr3:126405626
|
G | C | 55 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(52): Show | 57 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-1546G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405626 | ||||||
chr3:126405663
|
A | AAAATAAA others(1): Show |
11 | a0001c0001t0001g0013a0001c0001t0001g0355a0001c0001t0001g0356others(8): Show | 13 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-1493_50-1486dup others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 126405663 | |||||
chr3:126405685
|
A | G | 55 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(52): Show | 57 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-1487A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405685 | ||||||
chr3:126405811
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.50-1361A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405811 | ||||||
chr3:126405848
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50-1324C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405848 | ||||||
chr3:126405901
|
C | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0301a0001c0001t0001g0302others(3): Show | 7 | NA18968.hp2 NA18969.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-1271C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405901 | ||||||
chr3:126405976
|
C | G | 322 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(319): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.50-1196C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126405976 | ||||||
chr3:126406151
|
G | T | 1 | a0001c0013t0001g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.50-1021G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406151 | ||||||
chr3:126406189
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.50-983G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406189 | ||||||
chr3:126406208
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0090a0001c0001t0001g0095others(3): Show | 7 | HG00597.hp1 NA18941.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-964C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406208 | ||||||
chr3:126406261
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0105 | 3 | HG00597.hp1 NA18941.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.50-911C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406261 | ||||||
chr3:126406379
|
C | G | 8 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0274others(5): Show | 9 | HG01081.hp1 HG01928.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-793C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406379 | ||||||
chr3:126406419
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.50-753G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406419 | ||||||
chr3:126406457
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.50-715G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406457 | ||||||
chr3:126406623
|
G | A | 22 | a0001c0001t0001g0072a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 27 | HG00323.hp1 HG00741.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.50-549G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406623 | ||||||
chr3:126406664
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.50-508C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406664 | ||||||
chr3:126406814
|
C | G | 345 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(342): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.50-358C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406814 | ||||||
chr3:126406818
|
G | A | 28 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0148others(25): Show | 35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.50-354G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406818 | ||||||
chr3:126406872
|
A | G | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0270others(4): Show | 8 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-300A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126406872 | ||||||
chr3:126407023
|
C | A | 3 | a0001c0001t0001g0172a0001c0002t0001g0032a0001c0013t0001g0010 | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-149C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126407023 | ||||||
chr3:126407147
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0251others(3): Show | 6 | HG01243.hp1 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-25G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 2/16 | chr3 | 126407147 | ||||||
chr3:126407370
|
T | C | 2 | a0001c0002t0001g0359a0001c0002t0001g0364 | 2 | NA18992.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.130+118T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407370 | ||||||
chr3:126407383
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.130+131T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407383 | ||||||
chr3:126407429
|
T | A | 1 | a0001c0002t0001g0391 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.130+177T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407429 | ||||||
chr3:126407572
|
AT | A | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(21): Show | 25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+322delT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126407572 | |||||
chr3:126407573
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.130+321T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407573 | ||||||
chr3:126407574
|
T | G | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(21): Show | 25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+322T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407574 | ||||||
chr3:126407577
|
G | T | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(21): Show | 25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+325G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407577 | ||||||
chr3:126407578
|
GC | G | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(21): Show | 25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+327delC | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407578 | ||||||
chr3:126407581
|
T | C | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(21): Show | 25 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+329T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407581 | ||||||
chr3:126407664
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.130+412A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407664 | ||||||
chr3:126407669
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+417C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407669 | ||||||
chr3:126407796
|
C | T | 1 | a0001c0002t0001g0392 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130+544C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407796 | ||||||
chr3:126407941
|
T | C | 3 | a0001c0002t0001g0006a0003c0005t0001g0186a0012c0027t0001g0063 | 4 | HG01106.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+689T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126407941 | ||||||
chr3:126408119
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.130+867G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408119 | ||||||
chr3:126408142
|
G | C | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+890G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408142 | ||||||
chr3:126408192
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130+940C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408192 | ||||||
chr3:126408204
|
C | T | 3 | a0004c0007t0001g0139a0004c0007t0001g0141a0004c0028t0001g0140 | 3 | HG02109.hp2 HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+952C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408204 | ||||||
chr3:126408253
|
G | A | 4 | a0001c0008t0001g0007a0001c0008t0001g0092a0001c0008t0001g0099others(1): Show | 5 | NA18944.hp2 NA18974.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+1001G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408253 | ||||||
chr3:126408346
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.130+1094G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408346 | ||||||
chr3:126408473
|
C | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0042others(3): Show | 6 | HG00639.hp2 HG01346.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+1221C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408473 | ||||||
chr3:126408574
|
T | C | 1 | a0006c0011t0002g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+1322T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408574 | ||||||
chr3:126408632
|
C | T | 2 | a0001c0002t0001g0373a0001c0002t0001g0374 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.130+1380C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408632 | ||||||
chr3:126408705
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.130+1453G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408705 | ||||||
chr3:126408719
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130+1467C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408719 | ||||||
chr3:126408848
|
G | A | 6 | a0004c0007t0001g0126a0004c0007t0001g0139a0004c0007t0001g0141others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+1596G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408848 | ||||||
chr3:126408935
|
C | T | 55 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(52): Show | 57 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.130+1683C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126408935 | ||||||
chr3:126409106
|
C | T | 1 | a0002c0004t0001g0184 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.130+1854C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409106 | ||||||
chr3:126409169
|
A | T | 2 | a0001c0001t0001g0209a0014c0020t0001g0078 | 2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.130+1917A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409169 | ||||||
chr3:126409214
|
A | T | 1 | a0001c0002t0001g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130+1962A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409214 | ||||||
chr3:126409253
|
C | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(143): Show | 152 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.130+2001C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409253 | ||||||
chr3:126409266
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130+2014T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409266 | ||||||
chr3:126409287
|
T | C | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+2035T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409287 | ||||||
chr3:126409382
|
T | A | 1 | a0001c0001t0002g0310 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.130+2130T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409382 | ||||||
chr3:126409413
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130+2161G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409413 | ||||||
chr3:126409457
|
C | T | 1 | a0001c0001t0001g0357 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.130+2205C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409457 | ||||||
chr3:126409516
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.130+2264T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409516 | ||||||
chr3:126409609
|
AC | A | 3 | a0001c0001t0001g0077a0001c0003t0001g0076a0001c0003t0001g0232 | 3 | HG01243.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.130+2359delC | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126409609 | |||||
chr3:126409640
|
C | G | 2 | a0001c0002t0001g0373a0001c0002t0001g0374 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.130+2388C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409640 | ||||||
chr3:126409644
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.130+2392G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409644 | ||||||
chr3:126409658
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.130+2406C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409658 | ||||||
chr3:126409736
|
G | A | 28 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0148others(25): Show | 35 | HG01081.hp1 HG01255.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.130+2484G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409736 | ||||||
chr3:126409785
|
T | C | 53 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(50): Show | 55 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.130+2533T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409785 | ||||||
chr3:126409864
|
T | C | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | NA18953.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.130+2612T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126409864 | ||||||
chr3:126410005
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.130+2753A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410005 | ||||||
chr3:126410075
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.130+2823C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410075 | ||||||
chr3:126410106
|
C | G | 9 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0052others(6): Show | 10 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+2854C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410106 | ||||||
chr3:126410215
|
C | T | 10 | a0001c0001t0001g0038a0001c0001t0001g0201a0001c0001t0001g0204others(7): Show | 10 | HG01109.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+2963C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410215 | ||||||
chr3:126410230
|
C | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0017others(108): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.130+2978C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410230 | ||||||
chr3:126410273
|
G | C | 1 | a0001c0001t0001g0365 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.130+3021G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410273 | ||||||
chr3:126410337
|
C | T | 55 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0151others(52): Show | 57 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.130+3085C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410337 | ||||||
chr3:126410490
|
C | T | 1 | a0001c0003t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+3238C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410490 | ||||||
chr3:126410560
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0355a0001c0001t0001g0356others(8): Show | 13 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+3308G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410560 | ||||||
chr3:126410747
|
C | T | 1 | a0001c0001t0001g0014 | 2 | NA18939.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.131-3338C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410747 | ||||||
chr3:126410758
|
C | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-3327C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410758 | ||||||
chr3:126410803
|
C | T | 206 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(203): Show | 225 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.131-3282C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410803 | ||||||
chr3:126410809
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.131-3276T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126410809 | ||||||
chr3:126411015
|
G | A | 15 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(12): Show | 16 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.131-3070G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411015 | ||||||
chr3:126411223
|
C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0067others(22): Show | 28 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-2862C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411223 | ||||||
chr3:126411361
|
G | GT | 149 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0017others(146): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.131-2698dupT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
G | GTT | 76 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0046others(73): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-2699_131-2698d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
G | GTTT | 9 | a0001c0001t0001g0265a0001c0001t0001g0347a0001c0003t0001g0003others(6): Show | 11 | HG01255.hp2 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-2700_131-2698d others(5): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
G | GTTTT | 21 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0237others(18): Show | 24 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.131-2701_131-2698d others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
G | GTTTTT | 6 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0070others(3): Show | 6 | HG02300.hp1 HG02559.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-2702_131-2698d others(7): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
GT | G | 61 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0027others(58): Show | 63 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.131-2698delT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
GTT | G | 29 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0051others(26): Show | 30 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-2699_131-2698d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411361
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-2708_131-2698d others(13): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126411361 | |||||
chr3:126411524
|
T | C | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0270others(4): Show | 8 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-2561T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411524 | ||||||
chr3:126411623
|
C | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0042others(2): Show | 5 | HG00639.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-2462C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411623 | ||||||
chr3:126411701
|
T | C | 51 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0121others(48): Show | 58 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.131-2384T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411701 | ||||||
chr3:126411950
|
G | C | 1 | a0014c0020t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.131-2135G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411950 | ||||||
chr3:126411993
|
T | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0064others(22): Show | 28 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-2092T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126411993 | ||||||
chr3:126412029
|
T | C | 62 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0052others(59): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-2056T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412029 | ||||||
chr3:126412127
|
A | C | 28 | a0001c0001t0001g0028a0001c0001t0001g0062a0001c0001t0001g0150others(25): Show | 28 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-1958A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412127 | ||||||
chr3:126412132
|
C | T | 15 | a0001c0001t0001g0036a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 20 | HG00733.hp2 HG02451.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.131-1953C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412132 | ||||||
chr3:126412153
|
T | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0067others(32): Show | 39 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.131-1932T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412153 | ||||||
chr3:126412213
|
A | G | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.131-1872A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412213 | ||||||
chr3:126412244
|
T | G | 2 | a0002c0004t0001g0183a0002c0004t0001g0184 | 2 | HG02080.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.131-1841T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412244 | ||||||
chr3:126412281
|
T | A | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(224): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.131-1804T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412281 | ||||||
chr3:126412286
|
C | T | 201 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(198): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.131-1799C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412286 | ||||||
chr3:126412299
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0208a0001c0002t0001g0202 | 3 | HG01109.hp2 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.131-1786G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412299 | ||||||
chr3:126412396
|
C | G | 1 | a0001c0002t0001g0375 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.131-1689C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412396 | ||||||
chr3:126412487
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.131-1598T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412487 | ||||||
chr3:126412611
|
C | T | 298 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(295): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.131-1474C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412611 | ||||||
chr3:126412712
|
T | C | 35 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0033others(32): Show | 36 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.131-1373T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412712 | ||||||
chr3:126412844
|
T | C | 37 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0033others(34): Show | 38 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.131-1241T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412844 | ||||||
chr3:126412941
|
T | A | 1 | a0001c0001t0001g0311 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.131-1144T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126412941 | ||||||
chr3:126413035
|
A | G | 5 | a0001c0001t0001g0201a0001c0001t0001g0204a0001c0001t0001g0207others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1050A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413035 | ||||||
chr3:126413053
|
T | G | 18 | a0001c0003t0001g0001a0001c0003t0001g0003a0001c0003t0001g0009others(15): Show | 25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.131-1032T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413053 | ||||||
chr3:126413075
|
T | C | 3 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0074 | 3 | HG01346.hp2 HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.131-1010T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413075 | ||||||
chr3:126413188
|
T | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(269): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.131-897T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413188 | ||||||
chr3:126413301
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0188others(1): Show | 4 | HG00639.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-784C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413301 | ||||||
chr3:126413339
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-746C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413339 | ||||||
chr3:126413437
|
T | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(262): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.131-648T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413437 | ||||||
chr3:126413455
|
T | G | 5 | a0001c0003t0001g0003a0001c0003t0001g0034a0001c0003t0001g0076others(2): Show | 7 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-630T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413455 | ||||||
chr3:126413552
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0157others(6): Show | 10 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-533C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413552 | ||||||
chr3:126413851
|
C | G | 1 | a0006c0011t0002g0393 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.131-234C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413851 | ||||||
chr3:126413959
|
AG | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(159): Show | 175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.131-121delG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 126413959 | |||||
chr3:126413992
|
A | G | 37 | a0001c0001t0002g0037a0001c0003t0001g0001a0001c0003t0001g0003others(34): Show | 44 | HG00544.hp1 HG01243.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.131-93A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126413992 | ||||||
chr3:126414037
|
G | A | 36 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0033others(33): Show | 37 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.131-48G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 3/16 | chr3 | 126414037 | ||||||
chr3:126414278
|
C | G | 1 | a0001c0001t0001g0361 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.225+99C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414278 | ||||||
chr3:126414396
|
C | T | 160 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(157): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.225+217C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414396 | ||||||
chr3:126414559
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0077 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.225+380C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414559 | ||||||
chr3:126414560
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(20): Show | 25 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.225+381A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414560 | ||||||
chr3:126414644
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0074 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.225+465G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414644 | ||||||
chr3:126414661
|
C | T | 1 | a0018c0015t0001g0385 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.225+482C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414661 | ||||||
chr3:126414770
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.225+591C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126414770 | ||||||
chr3:126415020
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0379 | 2 | NA19057.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.225+841C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415020 | ||||||
chr3:126415072
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.225+893C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415072 | ||||||
chr3:126415298
|
C | G | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.226-1018C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415298 | ||||||
chr3:126415379
|
C | T | 6 | a0005c0009t0001g0029a0005c0009t0001g0145a0005c0009t0001g0205others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-937C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415379 | ||||||
chr3:126415413
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.226-903C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415413 | ||||||
chr3:126415434
|
C | A | 37 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0022others(34): Show | 40 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.226-882C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415434 | ||||||
chr3:126415507
|
G | A | 1 | a0005c0009t0001g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.226-809G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415507 | ||||||
chr3:126415593
|
T | A | 35 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0033others(32): Show | 36 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.226-723T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415593 | ||||||
chr3:126415633
|
G | A | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.226-683G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415633 | ||||||
chr3:126415670
|
G | A | 9 | a0001c0002t0001g0011a0001c0002t0001g0061a0001c0002t0001g0137others(6): Show | 10 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-646G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415670 | ||||||
chr3:126415675
|
C | G | 1 | a0002c0004t0001g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.226-641C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415675 | ||||||
chr3:126415676
|
G | C | 1 | a0002c0004t0001g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.226-640G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415676 | ||||||
chr3:126415782
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.226-534T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415782 | ||||||
chr3:126415783
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.226-533C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415783 | ||||||
chr3:126415793
|
T | C | 263 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(260): Show | 287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.226-523T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415793 | ||||||
chr3:126415862
|
A | G | 9 | a0001c0002t0001g0011a0001c0002t0001g0061a0001c0002t0001g0137others(6): Show | 10 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-454A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415862 | ||||||
chr3:126415927
|
C | T | 35 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0022others(32): Show | 38 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.226-389C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415927 | ||||||
chr3:126415944
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.226-372G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415944 | ||||||
chr3:126415963
|
G | A | 35 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0033others(32): Show | 36 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.226-353G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126415963 | ||||||
chr3:126416032
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.226-284G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416032 | ||||||
chr3:126416101
|
G | C | 1 | a0001c0001t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.226-215G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416101 | ||||||
chr3:126416168
|
C | T | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.226-148C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416168 | ||||||
chr3:126416179
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.226-137T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416179 | ||||||
chr3:126416219
|
G | T | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-97G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416219 | ||||||
chr3:126416227
|
C | CCGCGTCC others(15): Show |
77 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0022others(74): Show | 81 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.226-81_226-80insCG others(20): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 126416227 | |||||
chr3:126416235
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.226-81C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416235 | ||||||
chr3:126416256
|
G | A | 1 | a0003c0005t0001g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.226-60G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 4/16 | chr3 | 126416256 | ||||||
chr3:126416522
|
G | T | 94 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0022others(91): Show | 105 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.418+14G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416522 | ||||||
chr3:126416532
|
G | C | 3 | a0006c0011t0002g0168a0006c0011t0002g0239a0006c0011t0002g0393 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.418+24G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416532 | ||||||
chr3:126416671
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.418+163G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416671 | ||||||
chr3:126416824
|
A | G | 2 | a0001c0002t0001g0032a0001c0002t0001g0074 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.418+316A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416824 | ||||||
chr3:126416884
|
GTTA | G | 19 | a0001c0003t0001g0001a0001c0003t0001g0003a0001c0003t0001g0009others(16): Show | 26 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.418+379_418+381del others(3): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 126416884 | |||||
chr3:126416889
|
T | A | 1 | a0001c0013t0001g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.418+381T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416889 | ||||||
chr3:126416931
|
C | T | 94 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0022others(91): Show | 105 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.418+423C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416931 | ||||||
chr3:126416993
|
C | T | 1 | a0001c0002t0001g0359 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418+485C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416993 | ||||||
chr3:126416994
|
T | G | 1 | a0001c0002t0001g0359 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418+486T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416994 | ||||||
chr3:126416998
|
G | A | 3 | a0006c0011t0002g0168a0006c0011t0002g0239a0006c0011t0002g0393 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.418+490G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416998 | ||||||
chr3:126416999
|
G | T | 1 | a0001c0002t0001g0359 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418+491G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126416999 | ||||||
chr3:126417049
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(20): Show | 25 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.418+541C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417049 | ||||||
chr3:126417109
|
A | G | 1 | a0002c0004t0001g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.418+601A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417109 | ||||||
chr3:126417110
|
G | A | 1 | a0002c0004t0001g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.418+602G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417110 | ||||||
chr3:126417279
|
C | T | 1 | a0005c0009t0002g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.418+771C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417279 | ||||||
chr3:126417291
|
T | TAAGA | 95 | a0001c0001t0001g0365a0001c0002t0001g0006a0001c0002t0001g0011others(92): Show | 106 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.418+785_418+788dup others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 126417291 | |||||
chr3:126417315
|
G | A | 1 | a0001c0018t0001g0305 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.418+807G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417315 | ||||||
chr3:126417329
|
G | A | 36 | a0001c0001t0001g0365a0001c0002t0001g0023a0001c0002t0001g0024others(33): Show | 37 | HG00323.hp2 HG01099.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.418+821G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417329 | ||||||
chr3:126417365
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.418+857G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417365 | ||||||
chr3:126417566
|
G | A | 1 | a0001c0013t0001g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.419-892G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417566 | ||||||
chr3:126417616
|
G | A | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-842G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417616 | ||||||
chr3:126417633
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.419-825G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417633 | ||||||
chr3:126417636
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(113): Show | 126 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.419-822G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417636 | ||||||
chr3:126417638
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.419-820C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417638 | ||||||
chr3:126417651
|
C | G | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-807C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417651 | ||||||
chr3:126417659
|
G | A | 9 | a0001c0002t0001g0011a0001c0002t0001g0061a0001c0002t0001g0137others(6): Show | 10 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-799G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417659 | ||||||
chr3:126417693
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.419-765C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417693 | ||||||
chr3:126417729
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.419-729C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417729 | ||||||
chr3:126417730
|
G | A | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-728G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417730 | ||||||
chr3:126417753
|
G | C | 1 | a0001c0006t0001g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.419-705G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417753 | ||||||
chr3:126417881
|
C | T | 1 | a0014c0020t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.419-577C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417881 | ||||||
chr3:126417906
|
C | G | 10 | a0001c0001t0001g0036a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-552C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417906 | ||||||
chr3:126417927
|
A | C | 96 | a0001c0001t0001g0014a0001c0001t0001g0365a0001c0002t0001g0006others(93): Show | 108 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.419-531A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126417927 | ||||||
chr3:126418199
|
G | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(112): Show | 124 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.419-259G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418199 | ||||||
chr3:126418235
|
G | C | 238 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(235): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.419-223G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418235 | ||||||
chr3:126418237
|
G | A | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-221G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418237 | ||||||
chr3:126418418
|
G | A | 1 | a0001c0001t0001g0346 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.419-40G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418418 | ||||||
chr3:126418427
|
G | A | 3 | a0006c0011t0002g0168a0006c0011t0002g0239a0006c0011t0002g0393 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.419-31G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 5/16 | chr3 | 126418427 | ||||||
chr3:126418790
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0188others(1): Show | 4 | HG00639.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+16C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418790 | ||||||
chr3:126418791
|
G | A | 20 | a0001c0001t0001g0165a0001c0003t0001g0001a0001c0003t0001g0003others(17): Show | 27 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.650+17G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418791 | ||||||
chr3:126418834
|
C | T | 3 | a0006c0011t0002g0168a0006c0011t0002g0239a0006c0011t0002g0393 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.650+60C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418834 | ||||||
chr3:126418936
|
A | C | 1 | a0001c0001t0001g0341 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.651-140A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418936 | ||||||
chr3:126418949
|
T | A | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.651-127T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126418949 | ||||||
chr3:126419019
|
A | T | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.651-57A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 7/16 | chr3 | 126419019 | ||||||
chr3:126419198
|
C | T | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.731+42C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/16 | chr3 | 126419198 | ||||||
chr3:126419472
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.732-165G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 8/16 | chr3 | 126419472 | ||||||
chr3:126419844
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0112a0001c0001t0001g0342others(2): Show | 5 | HG00621.hp1 HG01993.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+26C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 9/16 | chr3 | 126419844 | ||||||
chr3:126419935
|
T | C | 301 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(298): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.914-45T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 9/16 | chr3 | 126419935 | ||||||
chr3:126420043
|
G | A | 1 | a0001c0006t0001g0276 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.955+22G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 10/16 | chr3 | 126420043 | ||||||
chr3:126420046
|
G | T | 102 | a0001c0001t0001g0150a0001c0001t0002g0198a0001c0002t0001g0006others(99): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.955+25G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 10/16 | chr3 | 126420046 | ||||||
chr3:126420077
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.956-26G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 10/16 | chr3 | 126420077 | ||||||
chr3:126420241
|
CG | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(20): Show | 25 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1082+15delG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 126420241 | |||||
chr3:126420243
|
G | C | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1082+14G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420243 | ||||||
chr3:126420275
|
G | C | 1 | a0001c0001t0001g0311 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1082+46G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420275 | ||||||
chr3:126420461
|
G | C | 2 | a0001c0013t0001g0010a0011c0017t0001g0144 | 3 | HG02895.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1082+232G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420461 | ||||||
chr3:126420557
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1082+328T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420557 | ||||||
chr3:126420777
|
G | A | 104 | a0001c0001t0001g0014a0001c0001t0001g0150a0001c0001t0002g0198others(101): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1082+548G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420777 | ||||||
chr3:126420836
|
A | G | 18 | a0001c0003t0001g0001a0001c0003t0001g0003a0001c0003t0001g0009others(15): Show | 25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1082+607A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420836 | ||||||
chr3:126420844
|
C | CTTATTGG others(8): Show |
103 | a0001c0001t0001g0014a0001c0001t0001g0150a0001c0001t0002g0198others(100): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1082+615_1082+616i others(17): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420844 | ||||||
chr3:126420932
|
G | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0241a0001c0001t0001g0260others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082+703G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420932 | ||||||
chr3:126420998
|
T | C | 16 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0048others(13): Show | 18 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.1082+769T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126420998 | ||||||
chr3:126421112
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1082+883C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421112 | ||||||
chr3:126421127
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 111 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1082+898C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421127 | ||||||
chr3:126421185
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1082+956G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421185 | ||||||
chr3:126421227
|
C | G | 2 | a0001c0002t0001g0032a0001c0002t0001g0074 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1082+998C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421227 | ||||||
chr3:126421330
|
T | C | 1 | a0014c0020t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1082+1101T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421330 | ||||||
chr3:126421405
|
C | T | 1 | a0001c0001t0001g0354 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1082+1176C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421405 | ||||||
chr3:126421489
|
C | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0326others(1): Show | 4 | NA18948.hp1 NA18993.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082+1260C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421489 | ||||||
chr3:126421493
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1082+1264G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421493 | ||||||
chr3:126421583
|
G | A | 1 | a0001c0003t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1082+1354G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421583 | ||||||
chr3:126421741
|
G | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1082+1512G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421741 | ||||||
chr3:126421811
|
C | A | 130 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(127): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1083-1514C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421811 | ||||||
chr3:126421864
|
A | G | 2 | a0001c0002t0001g0031a0001c0025t0001g0044 | 2 | HG01346.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1083-1461A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421864 | ||||||
chr3:126421868
|
C | T | 5 | a0004c0007t0001g0126a0004c0007t0001g0139a0004c0007t0001g0141others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083-1457C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421868 | ||||||
chr3:126421921
|
A | G | 8 | a0001c0001t0002g0037a0001c0002t0001g0202a0001c0013t0001g0010others(5): Show | 9 | HG01109.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083-1404A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126421921 | ||||||
chr3:126422036
|
G | C | 1 | a0002c0004t0001g0218 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1083-1289G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422036 | ||||||
chr3:126422038
|
T | C | 2 | a0001c0002t0001g0032a0001c0002t0001g0074 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1083-1287T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422038 | ||||||
chr3:126422141
|
C | A | 1 | a0001c0013t0001g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1083-1184C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422141 | ||||||
chr3:126422313
|
G | A | 102 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 111 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1083-1012G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422313 | ||||||
chr3:126422330
|
T | C | 12 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(9): Show | 12 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083-995T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422330 | ||||||
chr3:126422332
|
T | A | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1083-993T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422332 | ||||||
chr3:126422342
|
C | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(102): Show | 115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1083-983C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422342 | ||||||
chr3:126422365
|
C | G | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1083-960C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422365 | ||||||
chr3:126422366
|
C | G | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1083-959C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422366 | ||||||
chr3:126422437
|
A | G | 1 | a0001c0013t0001g0010 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1083-888A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422437 | ||||||
chr3:126422488
|
GC | G | 148 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(145): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083-829delC | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 126422488 | |||||
chr3:126422490
|
C | A | 1 | a0005c0024t0002g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1083-835C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422490 | ||||||
chr3:126422490
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1083-835C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422490 | ||||||
chr3:126422505
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0143 | 3 | HG02135.hp1 HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1083-820C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422505 | ||||||
chr3:126422519
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1083-806G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422519 | ||||||
chr3:126422592
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0334 | 2 | HG00099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1083-733C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422592 | ||||||
chr3:126422593
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1083-732G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422593 | ||||||
chr3:126422610
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1083-715G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422610 | ||||||
chr3:126422827
|
G | A | 9 | a0003c0005t0001g0012a0003c0005t0001g0075a0003c0005t0001g0149others(6): Show | 10 | HG00140.hp1 HG00639.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1083-498G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422827 | ||||||
chr3:126422860
|
C | T | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | NA18953.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1083-465C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126422860 | ||||||
chr3:126423014
|
A | G | 148 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(145): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083-311A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423014 | ||||||
chr3:126423018
|
G | A | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1083-307G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423018 | ||||||
chr3:126423050
|
C | A | 32 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(29): Show | 34 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1083-275C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423050 | ||||||
chr3:126423068
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(10): Show | 15 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1083-257G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423068 | ||||||
chr3:126423202
|
G | T | 1 | a0002c0004t0001g0213 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1083-123G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423202 | ||||||
chr3:126423320
|
C | T | 6 | a0001c0002t0001g0061a0001c0002t0001g0137a0001c0002t0001g0245others(3): Show | 6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1083-5C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 11/16 | chr3 | 126423320 | ||||||
chr3:126423463
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1135-30C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 12/16 | chr3 | 126423463 | ||||||
chr3:126423653
|
T | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(121): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1286+9T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423653 | ||||||
chr3:126423682
|
G | A | 2 | a0007c0010t0001g0187a0007c0010t0001g0190 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1286+38G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423682 | ||||||
chr3:126423740
|
C | T | 9 | a0001c0002t0001g0006a0001c0002t0001g0071a0001c0002t0001g0243others(6): Show | 12 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286+96C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423740 | ||||||
chr3:126423745
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1286+101G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423745 | ||||||
chr3:126423755
|
C | T | 13 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(10): Show | 13 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1286+111C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423755 | ||||||
chr3:126423839
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1286+195G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423839 | ||||||
chr3:126423852
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1286+208C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423852 | ||||||
chr3:126423857
|
G | A | 8 | a0001c0002t0001g0011a0001c0002t0001g0061a0001c0002t0001g0137others(5): Show | 9 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+213G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423857 | ||||||
chr3:126423974
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1286+330A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423974 | ||||||
chr3:126423983
|
G | A | 9 | a0001c0001t0001g0288a0001c0001t0001g0337a0001c0001t0001g0338others(6): Show | 9 | HG00673.hp1 HG02040.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286+339G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423983 | ||||||
chr3:126423990
|
C | A | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1286+346C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423990 | ||||||
chr3:126423998
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1286+354A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126423998 | ||||||
chr3:126424012
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1286+368G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424012 | ||||||
chr3:126424028
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1286+384G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424028 | ||||||
chr3:126424182
|
G | A | 1 | a0001c0006t0001g0276 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1286+538G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424182 | ||||||
chr3:126424182
|
G | C | 24 | a0001c0002t0001g0081a0001c0002t0001g0083a0001c0002t0001g0087others(21): Show | 24 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(21): Show |
intron_variant | MODIFIER | c.1286+538G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424182 | ||||||
chr3:126424183
|
G | C | 1 | a0001c0002t0001g0292 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1286+539G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424183 | ||||||
chr3:126424211
|
C | T | 9 | a0001c0002t0001g0006a0001c0002t0001g0071a0001c0002t0001g0243others(6): Show | 12 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286+567C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424211 | ||||||
chr3:126424442
|
A | G | 3 | a0006c0011t0002g0168a0006c0011t0002g0239a0006c0011t0002g0393 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1286+798A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424442 | ||||||
chr3:126424454
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+810A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424454 | ||||||
chr3:126424647
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1286+1003G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424647 | ||||||
chr3:126424765
|
A | G | 2 | a0001c0001t0001g0154a0011c0017t0001g0144 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1286+1121A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424765 | ||||||
chr3:126424808
|
G | C | 2 | a0001c0002t0001g0073a0001c0013t0001g0010 | 3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1286+1164G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424808 | ||||||
chr3:126424884
|
G | A | 237 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(234): Show | 260 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1286+1240G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424884 | ||||||
chr3:126424924
|
A | T | 1 | a0001c0002t0001g0292 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1286+1280A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126424924 | ||||||
chr3:126425171
|
T | C | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0326others(1): Show | 4 | NA18948.hp1 NA18993.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+1527T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425171 | ||||||
chr3:126425177
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0143 | 3 | HG02135.hp1 HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1286+1533C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425177 | ||||||
chr3:126425182
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1286+1538G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425182 | ||||||
chr3:126425192
|
T | C | 1 | a0001c0008t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1286+1548T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425192 | ||||||
chr3:126425330
|
A | G | 1 | a0001c0025t0001g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1286+1686A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425330 | ||||||
chr3:126425473
|
A | C | 8 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(5): Show | 8 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+1829A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425473 | ||||||
chr3:126425519
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1286+1875A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425519 | ||||||
chr3:126425549
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1286+1905G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425549 | ||||||
chr3:126425602
|
C | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(22): Show | 27 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1286+1958C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425602 | ||||||
chr3:126425641
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02083.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1286+1997C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425641 | ||||||
chr3:126425648
|
T | C | 12 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0206others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1286+2004T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425648 | ||||||
chr3:126425774
|
C | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+2130C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425774 | ||||||
chr3:126425789
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+2145C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425789 | ||||||
chr3:126425851
|
A | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(114): Show | 127 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1286+2207A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425851 | ||||||
chr3:126425903
|
C | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+2259C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425903 | ||||||
chr3:126425934
|
A | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+2290A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425934 | ||||||
chr3:126425967
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1286+2323A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126425967 | ||||||
chr3:126426013
|
G | T | 8 | a0001c0002t0001g0011a0001c0002t0001g0061a0001c0002t0001g0137others(5): Show | 9 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+2369G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426013 | ||||||
chr3:126426028
|
T | C | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+2384T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426028 | ||||||
chr3:126426217
|
C | A | 9 | a0001c0002t0001g0006a0001c0002t0001g0071a0001c0002t0001g0243others(6): Show | 12 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286+2573C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426217 | ||||||
chr3:126426280
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1286+2636T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426280 | ||||||
chr3:126426454
|
T | TA | 30 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0188others(27): Show | 30 | HG00408.hp2 HG00544.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1286+2825dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126426454 | |||||
chr3:126426454
|
T | TAA | 90 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(87): Show | 99 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1286+2824_1286+282 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126426454 | |||||
chr3:126426454
|
TA | T | 32 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0002t0001g0031others(29): Show | 34 | HG01243.hp2 HG01255.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.1286+2825delA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126426454 | |||||
chr3:126426477
|
T | C | 16 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(13): Show | 17 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1286+2833T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426477 | ||||||
chr3:126426578
|
C | T | 5 | a0004c0007t0001g0126a0004c0007t0001g0139a0004c0007t0001g0141others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+2934C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426578 | ||||||
chr3:126426682
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1286+3038G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426682 | ||||||
chr3:126426705
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1286+3061G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426705 | ||||||
chr3:126426765
|
A | G | 25 | a0001c0002t0001g0081a0001c0002t0001g0083a0001c0002t0001g0087others(22): Show | 25 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1286+3121A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426765 | ||||||
chr3:126426833
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1286+3189T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426833 | ||||||
chr3:126426977
|
G | A | 15 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(12): Show | 16 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1286+3333G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126426977 | ||||||
chr3:126427029
|
T | C | 1 | a0004c0007t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1286+3385T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427029 | ||||||
chr3:126427092
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1286+3448A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427092 | ||||||
chr3:126427162
|
T | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0177a0001c0001t0001g0314others(3): Show | 6 | HG02071.hp2 NA18940.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+3518T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427162 | ||||||
chr3:126427317
|
G | A | 2 | a0003c0005t0001g0075a0003c0005t0001g0240 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1286+3673G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427317 | ||||||
chr3:126427326
|
T | C | 9 | a0001c0002t0001g0006a0001c0002t0001g0071a0001c0002t0001g0243others(6): Show | 12 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286+3682T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427326 | ||||||
chr3:126427472
|
GGTGTCTG others(19): Show |
G | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1286+3836_1286+386 others(30): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126427472 | |||||
chr3:126427543
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+3899C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427543 | ||||||
chr3:126427776
|
TTTTAA | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0002t0001g0202 | 3 | HG02572.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+4136_1286+414 others(9): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126427776 | |||||
chr3:126427935
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+4291G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126427935 | ||||||
chr3:126428023
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0156others(1): Show | 4 | HG00639.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+4379G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428023 | ||||||
chr3:126428052
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1286+4408C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428052 | ||||||
chr3:126428054
|
T | C | 235 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(232): Show | 258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1286+4410T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428054 | ||||||
chr3:126428156
|
A | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1286+4512A>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428156 | ||||||
chr3:126428364
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-4705G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428364 | ||||||
chr3:126428368
|
TAAAG | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-4699_1287-469 others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126428368 | |||||
chr3:126428661
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1287-4408T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428661 | ||||||
chr3:126428699
|
A | G | 6 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287-4370A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428699 | ||||||
chr3:126428744
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1287-4325C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428744 | ||||||
chr3:126428881
|
T | C | 1 | a0001c0002t0001g0391 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1287-4188T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126428881 | ||||||
chr3:126429065
|
T | C | 235 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(232): Show | 258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1287-4004T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429065 | ||||||
chr3:126429066
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-4003G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429066 | ||||||
chr3:126429098
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1287-3971G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429098 | ||||||
chr3:126429107
|
C | CA | 23 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0098others(20): Show | 24 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1287-3935dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CA | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0105a0001c0001t0001g0116others(8): Show | 11 | HG00639.hp1 HG01891.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287-3935delA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAA | C | 37 | a0001c0001t0001g0038a0001c0001t0001g0204a0001c0001t0001g0234others(34): Show | 42 | HG00544.hp1 HG01891.hp1 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.1287-3936_1287-393 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAAA | C | 63 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0077others(60): Show | 69 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1287-3937_1287-393 others(7): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAAAA | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0286a0001c0002t0001g0022others(13): Show | 18 | HG00408.hp2 HG01256.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.1287-3938_1287-393 others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAAAAA | C | 16 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(13): Show | 16 | HG00733.hp1 HG01109.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1287-3939_1287-393 others(9): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0342 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1287-3944_1287-393 others(14): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1287-3945_1287-393 others(15): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429107
|
CAAAAAAA others(9): Show |
C | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-3950_1287-393 others(20): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429107 | |||||
chr3:126429129
|
A | G | 1 | a0001c0001t0001g0370 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1287-3940A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429129 | ||||||
chr3:126429162
|
G | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-3907G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429162 | ||||||
chr3:126429223
|
T | C | 2 | a0001c0001t0001g0154a0011c0017t0001g0144 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-3846T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429223 | ||||||
chr3:126429253
|
T | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-3816T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429253 | ||||||
chr3:126429455
|
T | C | 2 | a0001c0001t0001g0154a0011c0017t0001g0144 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-3614T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429455 | ||||||
chr3:126429622
|
G | GT | 303 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(300): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1287-3436dupT | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429622 | |||||
chr3:126429622
|
G | GTT | 27 | a0001c0001t0001g0080a0001c0001t0001g0295a0001c0001t0001g0370others(24): Show | 27 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1287-3437_1287-343 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429622 | |||||
chr3:126429765
|
T | TTATACTT others(3): Show |
1 | a0001c0001t0001g0389 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1287-3300_1287-329 others(14): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126429765 | |||||
chr3:126429785
|
G | A | 2 | a0001c0001t0001g0171a0017c0019t0001g0169 | 2 | NA19011.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1287-3284G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429785 | ||||||
chr3:126429811
|
T | C | 1 | a0001c0001t0001g0367 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1287-3258T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429811 | ||||||
chr3:126429909
|
T | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-3160T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429909 | ||||||
chr3:126429942
|
C | A | 16 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(13): Show | 17 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1287-3127C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126429942 | ||||||
chr3:126430009
|
T | C | 1 | a0002c0004t0001g0230 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1287-3060T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430009 | ||||||
chr3:126430031
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-3038C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430031 | ||||||
chr3:126430043
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1287-3026G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430043 | ||||||
chr3:126430050
|
T | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0071a0001c0002t0001g0243others(1): Show | 5 | HG00280.hp1 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-3019T>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430050 | ||||||
chr3:126430079
|
C | A | 1 | a0001c0001t0001g0377 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1287-2990C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430079 | ||||||
chr3:126430157
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-2912G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430157 | ||||||
chr3:126430232
|
T | TTAAG | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-2835_1287-283 others(8): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126430232 | |||||
chr3:126430450
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-2619A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430450 | ||||||
chr3:126430763
|
T | TG | 113 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(110): Show | 123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1287-2303dupG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126430763 | |||||
chr3:126430767
|
T | G | 11 | a0001c0001t0001g0386a0001c0002t0001g0032a0001c0002t0001g0074others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287-2302T>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430767 | ||||||
chr3:126430862
|
T | C | 50 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(47): Show | 52 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.1287-2207T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430862 | ||||||
chr3:126430912
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1287-2157A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430912 | ||||||
chr3:126430963
|
A | C | 9 | a0001c0002t0001g0006a0001c0002t0001g0071a0001c0002t0001g0243others(6): Show | 12 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1287-2106A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430963 | ||||||
chr3:126430964
|
T | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0177a0001c0001t0001g0314others(6): Show | 9 | HG02040.hp1 HG02071.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-2105T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126430964 | ||||||
chr3:126431011
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1287-2058C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431011 | ||||||
chr3:126431101
|
G | C | 2 | a0001c0001t0001g0154a0011c0017t0001g0144 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-1968G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431101 | ||||||
chr3:126431105
|
C | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(93): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1287-1964C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431105 | ||||||
chr3:126431385
|
C | A | 1 | a0001c0002t0001g0350 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1287-1684C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431385 | ||||||
chr3:126431419
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1287-1650C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431419 | ||||||
chr3:126431498
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-1571A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431498 | ||||||
chr3:126431529
|
C | T | 8 | a0001c0002t0001g0011a0001c0002t0001g0061a0001c0002t0001g0137others(5): Show | 9 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287-1540C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431529 | ||||||
chr3:126431683
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG01192.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1287-1386G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431683 | ||||||
chr3:126431687
|
A | C | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-1382A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431687 | ||||||
chr3:126431740
|
T | TTC | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-1328_1287-132 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126431740 | |||||
chr3:126431794
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1287-1275C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126431794 | ||||||
chr3:126431886
|
ACT | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG01169.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1287-1180_1287-117 others(6): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126431886 | |||||
chr3:126432007
|
G | A | 17 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(14): Show | 18 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1287-1062G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432007 | ||||||
chr3:126432052
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(112): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1287-1017A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432052 | ||||||
chr3:126432077
|
G | A | 1 | a0001c0001t0005g0086 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1287-992G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432077 | ||||||
chr3:126432077
|
G | C | 2 | a0001c0002t0001g0032a0001c0002t0001g0074 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1287-992G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432077 | ||||||
chr3:126432085
|
C | T | 2 | a0001c0002t0001g0073a0001c0013t0001g0010 | 3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1287-984C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432085 | ||||||
chr3:126432136
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-933G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432136 | ||||||
chr3:126432187
|
G | A | 25 | a0001c0002t0001g0081a0001c0002t0001g0083a0001c0002t0001g0087others(22): Show | 25 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1287-882G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432187 | ||||||
chr3:126432232
|
T | C | 17 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(14): Show | 18 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1287-837T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432232 | ||||||
chr3:126432266
|
G | A | 2 | a0001c0001t0001g0154a0011c0017t0001g0144 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287-803G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432266 | ||||||
chr3:126432282
|
C | CA | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(93): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1287-765dupA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | |||||
chr3:126432282
|
C | CAA | 14 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0138others(11): Show | 15 | HG00735.hp1 HG01258.hp1 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.1287-766_1287-765d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | |||||
chr3:126432282
|
CA | C | 142 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0025others(139): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1287-765delA | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | |||||
chr3:126432282
|
CAA | C | 10 | a0001c0001t0001g0090a0001c0001t0001g0111a0001c0001t0001g0355others(7): Show | 11 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-766_1287-765d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432282 | |||||
chr3:126432348
|
T | C | 16 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(13): Show | 17 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1287-721T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432348 | ||||||
chr3:126432429
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-640G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432429 | ||||||
chr3:126432518
|
G | T | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-551G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432518 | ||||||
chr3:126432536
|
ATGC | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(22): Show | 27 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1287-529_1287-527d others(5): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432536 | |||||
chr3:126432630
|
T | TCAGGGTA others(1): Show |
50 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(47): Show | 52 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.1287-438_1287-431d others(10): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 126432630 | |||||
chr3:126432632
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1287-437A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432632 | ||||||
chr3:126432693
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1287-376A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432693 | ||||||
chr3:126432788
|
CTT | C | 5 | a0001c0003t0001g0003a0001c0003t0001g0034a0001c0003t0001g0076others(2): Show | 7 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-280_1287-279d others(4): Show |
CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432788 | ||||||
chr3:126432837
|
C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(94): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1287-232C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432837 | ||||||
chr3:126432954
|
T | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1287-115T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126432954 | ||||||
chr3:126433051
|
G | A | 10 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(7): Show | 10 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1287-18G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 13/16 | chr3 | 126433051 | ||||||
chr3:126433281
|
G | A | 33 | a0001c0001t0002g0037a0001c0003t0001g0001a0001c0003t0001g0009others(30): Show | 38 | HG00544.hp1 HG01891.hp1 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.1422+77G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433281 | ||||||
chr3:126433308
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1422+104C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433308 | ||||||
chr3:126433487
|
G | T | 6 | a0001c0001t0001g0304a0001c0001t0001g0334a0001c0003t0001g0003others(3): Show | 8 | HG00099.hp1 HG00140.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422+283G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433487 | ||||||
chr3:126433499
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1422+295C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433499 | ||||||
chr3:126433541
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1422+337G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433541 | ||||||
chr3:126433623
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1422+419G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433623 | ||||||
chr3:126433631
|
C | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1422+427C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433631 | ||||||
chr3:126433674
|
C | T | 17 | a0001c0001t0002g0198a0001c0001t0002g0248a0001c0001t0002g0249others(14): Show | 18 | HG00733.hp1 HG01346.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1422+470C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433674 | ||||||
chr3:126433675
|
AG | A | 3 | a0006c0011t0002g0168a0006c0011t0002g0239a0006c0011t0002g0393 | 3 | HG02886.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1422+473delG | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 126433675 | |||||
chr3:126433688
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02083.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1422+484A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433688 | ||||||
chr3:126433764
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1423-412C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433764 | ||||||
chr3:126433821
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1423-355C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433821 | ||||||
chr3:126433925
|
C | T | 6 | a0004c0007t0001g0126a0004c0007t0001g0139a0004c0007t0001g0141others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423-251C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433925 | ||||||
chr3:126433986
|
G | A | 1 | a0011c0017t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1423-190G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126433986 | ||||||
chr3:126434001
|
C | T | 2 | a0001c0001t0001g0154a0011c0017t0001g0144 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1423-175C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126434001 | ||||||
chr3:126434137
|
C | T | 25 | a0001c0002t0001g0081a0001c0002t0001g0083a0001c0002t0001g0087others(22): Show | 25 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.1423-39C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126434137 | ||||||
chr3:126434174
|
A | C | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1423-2A>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 14/16 | chr3 | 126434174 | ||||||
chr3:126434416
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0038others(8): Show | 13 | HG01070.hp2 HG01071.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1628+35C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434416 | ||||||
chr3:126434467
|
C | T | 32 | a0001c0001t0002g0037a0001c0003t0001g0001a0001c0003t0001g0009others(29): Show | 37 | HG00544.hp1 HG01891.hp1 HG02080.hp2 others(34): Show |
intron_variant | MODIFIER | c.1628+86C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434467 | ||||||
chr3:126434518
|
T | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(138): Show | 153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1628+137T>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434518 | ||||||
chr3:126434600
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1628+219G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434600 | ||||||
chr3:126434734
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0160a0001c0001t0001g0286others(10): Show | 15 | HG00408.hp2 HG01256.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1628+353C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434734 | ||||||
chr3:126434774
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1628+393G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434774 | ||||||
chr3:126434795
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1628+414G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434795 | ||||||
chr3:126434858
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1628+477G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434858 | ||||||
chr3:126434921
|
G | T | 1 | a0010c0029t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1628+540G>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434921 | ||||||
chr3:126434949
|
C | G | 43 | a0001c0001t0002g0037a0001c0002t0001g0032a0001c0002t0001g0071others(40): Show | 50 | HG00280.hp1 HG00544.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1628+568C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434949 | ||||||
chr3:126434949
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1628+568C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126434949 | ||||||
chr3:126435004
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0074 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1629-555G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435004 | ||||||
chr3:126435034
|
C | T | 6 | a0001c0002t0001g0061a0001c0002t0001g0137a0001c0002t0001g0245others(3): Show | 6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1629-525C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435034 | ||||||
chr3:126435079
|
A | G | 7 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0251others(4): Show | 7 | HG00733.hp1 HG01358.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1629-480A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435079 | ||||||
chr3:126435101
|
C | T | 1 | a0001c0001t0001g0365 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1629-458C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435101 | ||||||
chr3:126435151
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1629-408G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435151 | ||||||
chr3:126435313
|
A | G | 6 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0003t0001g0015others(3): Show | 8 | HG02145.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629-246A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435313 | ||||||
chr3:126435358
|
C | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(86): Show | 99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1629-201C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435358 | ||||||
chr3:126435391
|
G | A | 7 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0326others(4): Show | 7 | HG00423.hp2 NA18948.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1629-168G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435391 | ||||||
chr3:126435475
|
C | T | 1 | a0001c0001t0001g0366 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1629-84C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435475 | ||||||
chr3:126435476
|
G | A | 27 | a0001c0001t0001g0214a0001c0001t0001g0225a0001c0001t0001g0226others(24): Show | 27 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(24): Show |
intron_variant | MODIFIER | c.1629-83G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435476 | ||||||
chr3:126435488
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1629-71G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435488 | ||||||
chr3:126435538
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1629-21A>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435538 | ||||||
chr3:126435554
|
C | A | 24 | a0001c0002t0001g0083a0001c0002t0001g0087a0001c0002t0001g0096others(21): Show | 24 | HG02523.hp1 HG02683.hp1 HG02698.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1629-5C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 15/16 | chr3 | 126435554 | ||||||
chr3:126435698
|
G | C | 1 | a0001c0001t0001g0274 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1722+46G>C | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126435698 | ||||||
chr3:126435791
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0019others(102): Show | 120 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1722+139G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126435791 | ||||||
chr3:126435979
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1723-312C>T | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126435979 | ||||||
chr3:126436015
|
C | A | 3 | a0002c0004t0001g0146a0007c0010t0001g0187a0007c0010t0001g0190 | 3 | HG01109.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1723-276C>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126436015 | ||||||
chr3:126436162
|
C | G | 8 | a0002c0004t0001g0146a0004c0007t0001g0126a0004c0007t0001g0139others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1723-129C>G | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126436162 | ||||||
chr3:126436173
|
G | A | 16 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 16 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1723-118G>A | CFAP100 | ENSG00000163885.12 | transcript | ENST00000352312.6 | protein_coding | 16/16 | chr3 | 126436173 |