geneid | 283638 |
---|---|
ensemblid | ENSG00000099814.17 |
hgncid | 20362 |
symbol | CEP170B |
name | centrosomal protein 170B |
refseq_nuc | NM_001112726.3 |
refseq_prot | NP_001106197.1 |
ensembl_nuc | ENST00000414716.8 |
ensembl_prot | ENSP00000404151.2 |
mane_status | MANE Select |
chr | chr14 |
start | 104865268 |
end | 104896747 |
strand | + |
ver | v1.2 |
region | chr14:104865268-104896747 |
region5000 | chr14:104860268-104901747 |
regionname0 | CEP170B_chr14_104865268_104896747 |
regionname5000 | CEP170B_chr14_104860268_104901747 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1554 | 251 | 70 | 61 | 73 | 10 | 35 | 52 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002 | 0/0 | 1552 | 33 | 2 | 12 | 12 | 0 | 7 | 7 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003 | 0/0 | 1554 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0004 | 0/0 | 1554 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0005 | 0/0 | 1554 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0006 | 0/0 | 1552 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0007 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0008 | 0/0 | 1554 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0009 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0010 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0011 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0012 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0013 | 0/0 | 1552 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0014 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0015 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0016 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0017 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0018 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0019 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0020 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0021 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0022 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0023 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0024 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0025 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0026 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0027 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0028 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0029 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0030 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0031 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0032 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 4665 | 104 | 16 | 18 | 55 | 4 | 10 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0002 | 0/0 | 4665 | 25 | 0 | 14 | 3 | 2 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0003 | 0/0 | 4665 | 22 | 3 | 11 | 0 | 1 | 7 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0004 | 0/0 | 4659 | 16 | 1 | 4 | 9 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0005 | 0/0 | 4665 | 10 | 9 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0006 | 0/0 | 4665 | 8 | 0 | 2 | 1 | 0 | 5 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0007 | 0/0 | 4665 | 8 | 8 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0008 | 0/0 | 4665 | 8 | 7 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0009 | 0/0 | 4659 | 7 | 0 | 7 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0010 | 0/0 | 4665 | 6 | 0 | 2 | 0 | 2 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0011 | 0/0 | 4665 | 5 | 0 | 1 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0012 | 0/0 | 4659 | 4 | 0 | 0 | 0 | 0 | 4 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0013 | 0/1 | 4665 | 3 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0014 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0015 | 0/0 | 4665 | 3 | 1 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0016 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0017 | 0/0 | 4665 | 3 | 0 | 2 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0018 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0019 | 0/0 | 4665 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0020 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0021 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0022 | 0/0 | 4665 | 3 | 0 | 1 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0023 | 0/0 | 4665 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0024 | 0/0 | 4665 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0025 | 0/0 | 4665 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0026 | 0/0 | 4665 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0027 | 0/0 | 4665 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0028 | 0/0 | 4659 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0029 | 0/0 | 4659 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0030 | 0/0 | 4659 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0031 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0032 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0033 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0034 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0035 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0036 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0037 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0038 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0039 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0040 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0041 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0042 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0043 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0044 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0045 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0046 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0047 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0048 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0049 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0050 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0051 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0052 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0053 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0054 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0055 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0056 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0057 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0058 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0059 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0060 | 0/0 | 4659 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0061 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0062 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0063 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0064 | 0/0 | 4659 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0065 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0066 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0067 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0068 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0069 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0070 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0071 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0072 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0073 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0074 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0075 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0076 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0077 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0078 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0079 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0080 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0081 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0082 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0083 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0084 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0085 | 0/0 | 4683 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0086 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0087 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0088 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
c0089 | 0/0 | 4659 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2064 | 124 | 36 | 21 | 53 | 3 | 11 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0002 | 0/1 | 2064 | 122 | 21 | 48 | 21 | 6 | 25 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0003 | 0/0 | 2068 | 24 | 22 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0004 | 0/0 | 2064 | 21 | 0 | 2 | 19 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0005 | 0/0 | 2064 | 8 | 0 | 1 | 1 | 0 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0006 | 0/0 | 2064 | 4 | 4 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0007 | 0/0 | 2064 | 3 | 0 | 1 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0008 | 0/0 | 2064 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0009 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0010 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0011 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0012 | 0/0 | 2064 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0013 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0014 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0015 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0016 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0017 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0018 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0019 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0020 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0021 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0022 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0023 | 1/0 | 2063 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0024 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0025 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0026 | 0/0 | 2068 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
t0027 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0003 | 0/1 | 4 | 0 | 0 | 0 | 1 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0005 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4665 | 104 | 16 | 18 | 55 | 4 | 10 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0002 | 0/0 | 4665 | 25 | 0 | 14 | 3 | 2 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0003 | 0/0 | 4665 | 22 | 3 | 11 | 0 | 1 | 7 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0005 | 0/0 | 4665 | 10 | 9 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0006 | 0/0 | 4665 | 8 | 0 | 2 | 1 | 0 | 5 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0007 | 0/0 | 4665 | 8 | 8 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0008 | 0/0 | 4665 | 8 | 7 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0010 | 0/0 | 4665 | 6 | 0 | 2 | 0 | 2 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0011 | 0/0 | 4665 | 5 | 0 | 1 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0013 | 0/1 | 4665 | 3 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0014 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0015 | 0/0 | 4665 | 3 | 1 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0017 | 0/0 | 4665 | 3 | 0 | 2 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0018 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0019 | 0/0 | 4665 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0020 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0022 | 0/0 | 4665 | 3 | 0 | 1 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0023 | 0/0 | 4665 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0032 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0034 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0035 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0037 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0038 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0041 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0042 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0048 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0053 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0054 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0055 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0058 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0059 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0061 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0062 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0065 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0066 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0069 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0070 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0071 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0073 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0074 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0075 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0077 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0080 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0082 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0083 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0087 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0088 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0004 | 0/0 | 4659 | 16 | 1 | 4 | 9 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0009 | 0/0 | 4659 | 7 | 0 | 7 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0012 | 0/0 | 4659 | 4 | 0 | 0 | 0 | 0 | 4 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0028 | 0/0 | 4659 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0029 | 0/0 | 4659 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0060 | 0/0 | 4659 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0064 | 0/0 | 4659 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003c0026 | 0/0 | 4665 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003c0067 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003c0078 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0004c0021 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0004c0081 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0005c0016 | 0/0 | 4665 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0006c0030 | 0/0 | 4659 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0007c0046 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0007c0047 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0008c0063 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0008c0086 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0009c0024 | 0/0 | 4665 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0010c0025 | 0/0 | 4665 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0011c0027 | 0/0 | 4665 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0012c0031 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0013c0089 | 0/0 | 4659 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0014c0057 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0015c0039 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0016c0076 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0017c0033 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0018c0068 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0019c0044 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0020c0084 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0021c0085 | 0/0 | 4683 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0022c0079 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0023c0049 | 0/0 | 4665 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0024c0036 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0025c0043 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0026c0072 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0027c0050 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0028c0045 | 0/0 | 4665 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0029c0052 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0030c0040 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0031c0051 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0032c0056 | 0/0 | 4665 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6728 | 80 | 14 | 16 | 38 | 3 | 9 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0002 | 0/0 | 6728 | 3 | 0 | 0 | 2 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0004 | 0/0 | 6728 | 13 | 0 | 2 | 11 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0010 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0015 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0016 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0022 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0023 | 1/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0025 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0026 | 0/0 | 6732 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0001t0027 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0002t0002 | 0/0 | 6728 | 25 | 0 | 14 | 3 | 2 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0003t0002 | 0/0 | 6728 | 20 | 3 | 11 | 0 | 0 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0003t0020 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0003t0021 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0005t0003 | 0/0 | 6732 | 10 | 9 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0006t0005 | 0/0 | 6728 | 6 | 0 | 1 | 0 | 0 | 5 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0006t0007 | 0/0 | 6728 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0007t0001 | 0/0 | 6728 | 5 | 5 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0007t0008 | 0/0 | 6728 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0008t0003 | 0/0 | 6732 | 8 | 7 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0010t0002 | 0/0 | 6728 | 6 | 0 | 2 | 0 | 2 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0011t0001 | 0/0 | 6728 | 5 | 0 | 1 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0013t0002 | 0/1 | 6728 | 3 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0014t0001 | 0/0 | 6728 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0015t0001 | 0/0 | 6728 | 3 | 1 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0017t0002 | 0/0 | 6728 | 3 | 0 | 2 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0018t0003 | 0/0 | 6732 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0019t0002 | 0/0 | 6728 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0020t0002 | 0/0 | 6728 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0022t0001 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0022t0004 | 0/0 | 6728 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0023t0004 | 0/0 | 6728 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0032t0024 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0034t0004 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0035t0013 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0037t0005 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0038t0005 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0041t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0042t0001 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0048t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0053t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0054t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0055t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0058t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0059t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0061t0017 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0062t0002 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0065t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0066t0001 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0069t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0070t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0071t0003 | 0/0 | 6732 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0073t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0074t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0075t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0077t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0080t0018 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0082t0002 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0083t0002 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0087t0002 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0001c0088t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0004t0002 | 0/0 | 6722 | 16 | 1 | 4 | 9 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0009t0002 | 0/0 | 6722 | 6 | 0 | 6 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0009t0012 | 0/0 | 6722 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0012t0002 | 0/0 | 6722 | 4 | 0 | 0 | 0 | 0 | 4 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0028t0002 | 0/0 | 6722 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0029t0002 | 0/0 | 6722 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0060t0002 | 0/0 | 6722 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0002c0064t0002 | 0/0 | 6722 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003c0026t0002 | 0/0 | 6728 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003c0067t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0003c0078t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0004c0021t0006 | 0/0 | 6728 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0004c0081t0006 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0005c0016t0001 | 0/0 | 6728 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0005c0016t0014 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0006c0030t0002 | 0/0 | 6722 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0007c0046t0004 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0007c0047t0004 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0008c0063t0002 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0008c0086t0002 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0009c0024t0001 | 0/0 | 6728 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0010c0025t0002 | 0/0 | 6728 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0011c0027t0003 | 0/0 | 6732 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0012c0031t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0013c0089t0002 | 0/0 | 6722 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0014c0057t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0015c0039t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0016c0076t0004 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0017c0033t0009 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0018c0068t0019 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0019c0044t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0020c0084t0002 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0021c0085t0002 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0022c0079t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0023c0049t0001 | 0/0 | 6728 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0024c0036t0007 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0025c0043t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0026c0072t0002 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0027c0050t0001 | 0/0 | 6728 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0028c0045t0001 | 0/0 | 6728 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0029c0052t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0030c0040t0011 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0031c0051t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
a0032c0056t0001 | 0/0 | 6728 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | copy fasta | chr14 | 104860268 | 104901747 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0015g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0022g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0023g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0025g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0026g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0027g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0020g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0021g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0007g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0013t0002g0003 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0013t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0014t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0014t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0015t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0015t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0015t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0017t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0017t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0017t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0018t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0019t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0019t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0019t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0020t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0020t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0020t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0022t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0022t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0022t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0023t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0032t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0034t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0035t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0037t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0038t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0041t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0042t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0048t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0053t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0054t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0055t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0058t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0059t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0061t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0062t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0065t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0066t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0069t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0070t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0071t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0073t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0074t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0075t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0077t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0080t0018g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0082t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0083t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0087t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0088t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0012g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0012t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0012t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0012t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0028t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0028t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0029t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0060t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0064t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0026t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0026t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0067t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0078t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0021t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0021t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0021t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0081t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0005c0016t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0005c0016t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0006c0030t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0006c0030t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0007c0046t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0007c0047t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0008c0063t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0008c0086t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0009c0024t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0009c0024t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0010c0025t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0010c0025t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0011c0027t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0011c0027t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0012c0031t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0013c0089t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0014c0057t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0015c0039t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0016c0076t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0017c0033t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0018c0068t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0019c0044t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0020c0084t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0021c0085t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0022c0079t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0023c0049t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0024c0036t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0025c0043t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0026c0072t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0027c0050t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0028c0045t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0029c0052t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0030c0040t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0031c0051t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0032c0056t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0234 | EUR | GBR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00280 | hp1 | a0001 | c0010 | t0002 | g0053 | EUR | FIN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00280 | hp2 | a0001 | c0003 | t0020 | g0244 | EUR | FIN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00408 | hp2 | a0006 | c0030 | t0002 | g0210 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00438 | hp1 | a0024 | c0036 | t0007 | g0159 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00438 | hp2 | a0009 | c0024 | t0001 | g0098 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00544 | hp1 | a0002 | c0004 | t0002 | g0030 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00621 | hp1 | a0015 | c0039 | t0001 | g0106 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00733 | hp1 | a0028 | c0045 | t0001 | g0144 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00733 | hp2 | a0001 | c0019 | t0002 | g0167 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0224 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01069 | hp2 | a0001 | c0017 | t0002 | g0174 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01071 | hp1 | a0002 | c0004 | t0002 | g0203 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01071 | hp2 | a0001 | c0017 | t0002 | g0173 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01074 | hp2 | a0013 | c0089 | t0002 | g0006 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0204 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01099 | hp1 | a0001 | c0006 | t0005 | g0036 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01099 | hp2 | a0001 | c0083 | t0002 | g0226 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0190 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01106 | hp2 | a0002 | c0004 | t0002 | g0179 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0221 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0232 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01167 | hp2 | a0001 | c0008 | t0003 | g0261 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01168 | hp2 | a0002 | c0009 | t0012 | g0183 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0191 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0239 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01255 | hp1 | a0001 | c0005 | t0003 | g0251 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01255 | hp2 | a0001 | c0010 | t0002 | g0051 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01256 | hp1 | a0002 | c0009 | t0002 | g0006 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01257 | hp1 | a0020 | c0084 | t0002 | g0236 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01257 | hp2 | a0002 | c0004 | t0002 | g0028 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01258 | hp1 | a0002 | c0004 | t0002 | g0028 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01261 | hp1 | a0001 | c0066 | t0001 | g0119 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01261 | hp2 | a0001 | c0087 | t0002 | g0209 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01346 | hp1 | a0001 | c0015 | t0001 | g0064 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01358 | hp2 | a0001 | c0003 | t0002 | g0222 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01361 | hp1 | a0001 | c0011 | t0001 | g0133 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01361 | hp2 | a0002 | c0029 | t0002 | g0031 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01496 | hp1 | a0001 | c0006 | t0007 | g0024 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01496 | hp2 | a0001 | c0062 | t0002 | g0177 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01516 | hp1 | a0001 | c0017 | t0002 | g0170 | EUR | IBS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01884 | hp1 | a0003 | c0026 | t0002 | g0250 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01884 | hp2 | a0001 | c0080 | t0018 | g0078 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01891 | hp1 | a0001 | c0070 | t0001 | g0166 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01891 | hp2 | a0001 | c0007 | t0001 | g0018 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0235 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01928 | hp2 | a0001 | c0003 | t0002 | g0241 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01934 | hp1 | a0001 | c0019 | t0002 | g0168 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01934 | hp2 | a0002 | c0009 | t0002 | g0006 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01975 | hp2 | a0001 | c0010 | t0002 | g0052 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0240 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01981 | hp1 | a0002 | c0009 | t0002 | g0185 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01993 | hp1 | a0002 | c0009 | t0002 | g0006 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02004 | hp1 | a0002 | c0009 | t0002 | g0207 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02004 | hp2 | a0001 | c0022 | t0001 | g0238 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02015 | hp2 | a0001 | c0001 | t0025 | g0016 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02027 | hp1 | a0025 | c0043 | t0001 | g0102 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02027 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02055 | hp1 | a0011 | c0027 | t0003 | g0259 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02055 | hp2 | a0001 | c0007 | t0008 | g0136 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02080 | hp1 | a0001 | c0011 | t0001 | g0124 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02132 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02135 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02145 | hp1 | a0002 | c0004 | t0002 | g0181 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02148 | hp1 | a0002 | c0009 | t0002 | g0215 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | CDX | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02257 | hp1 | a0002 | c0029 | t0002 | g0031 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02257 | hp2 | a0001 | c0020 | t0002 | g0026 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02258 | hp1 | a0001 | c0005 | t0003 | g0260 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02258 | hp2 | a0001 | c0005 | t0003 | g0253 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02280 | hp2 | a0001 | c0018 | t0003 | g0013 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02293 | hp2 | a0001 | c0003 | t0002 | g0242 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02451 | hp1 | a0001 | c0020 | t0002 | g0164 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02451 | hp2 | a0001 | c0059 | t0001 | g0075 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02523 | hp2 | a0002 | c0004 | t0002 | g0217 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02572 | hp1 | a0005 | c0016 | t0001 | g0021 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02572 | hp2 | a0001 | c0005 | t0003 | g0256 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02615 | hp1 | a0032 | c0056 | t0001 | g0101 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02615 | hp2 | a0001 | c0005 | t0003 | g0032 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02622 | hp1 | a0001 | c0053 | t0001 | g0083 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02622 | hp2 | a0004 | c0021 | t0006 | g0245 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02630 | hp1 | a0001 | c0007 | t0001 | g0146 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02630 | hp2 | a0001 | c0005 | t0003 | g0257 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02647 | hp1 | a0001 | c0075 | t0002 | g0163 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02647 | hp2 | a0001 | c0005 | t0003 | g0032 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02683 | hp2 | a0001 | c0003 | t0021 | g0199 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02698 | hp1 | a0001 | c0082 | t0002 | g0200 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02698 | hp2 | a0001 | c0006 | t0005 | g0023 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0225 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02717 | hp2 | a0003 | c0078 | t0002 | g0249 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02723 | hp1 | a0030 | c0040 | t0011 | g0273 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02723 | hp2 | a0001 | c0071 | t0003 | g0252 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02735 | hp1 | a0002 | c0012 | t0002 | g0211 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02735 | hp2 | a0001 | c0006 | t0005 | g0154 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0187 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02809 | hp1 | a0001 | c0073 | t0002 | g0162 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02809 | hp2 | a0029 | c0052 | t0001 | g0047 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02818 | hp1 | a0001 | c0008 | t0003 | g0262 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02818 | hp2 | a0001 | c0020 | t0002 | g0160 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02896 | hp1 | a0001 | c0008 | t0003 | g0014 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02897 | hp2 | a0001 | c0008 | t0003 | g0014 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02922 | hp1 | a0001 | c0077 | t0001 | g0087 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02922 | hp2 | a0001 | c0054 | t0001 | g0079 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02965 | hp1 | a0001 | c0007 | t0008 | g0137 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02965 | hp2 | a0001 | c0018 | t0003 | g0013 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02970 | hp1 | a0001 | c0005 | t0003 | g0255 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02976 | hp1 | a0003 | c0067 | t0002 | g0025 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02976 | hp2 | a0001 | c0015 | t0001 | g0108 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0189 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03041 | hp1 | a0018 | c0068 | t0019 | g0080 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03041 | hp2 | a0001 | c0005 | t0003 | g0254 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03098 | hp1 | a0001 | c0001 | t0026 | g0264 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03098 | hp2 | a0001 | c0008 | t0003 | g0266 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03130 | hp1 | a0001 | c0048 | t0001 | g0130 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03130 | hp2 | a0001 | c0001 | t0022 | g0090 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03139 | hp1 | a0001 | c0014 | t0001 | g0017 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03139 | hp2 | a0001 | c0007 | t0008 | g0140 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03195 | hp1 | a0001 | c0018 | t0003 | g0013 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03195 | hp2 | a0001 | c0065 | t0002 | g0268 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03225 | hp2 | a0001 | c0008 | t0003 | g0258 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03239 | hp2 | a0001 | c0010 | t0002 | g0003 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03453 | hp1 | a0001 | c0032 | t0024 | g0175 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03453 | hp2 | a0010 | c0025 | t0002 | g0270 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03486 | hp1 | a0001 | c0008 | t0003 | g0265 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03486 | hp2 | a0001 | c0007 | t0001 | g0114 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03490 | hp1 | a0001 | c0013 | t0002 | g0037 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03490 | hp2 | a0002 | c0012 | t0002 | g0029 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03492 | hp2 | a0002 | c0012 | t0002 | g0029 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0005 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03579 | hp1 | a0005 | c0016 | t0001 | g0021 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03579 | hp2 | a0005 | c0016 | t0014 | g0088 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03654 | hp1 | a0008 | c0063 | t0002 | g0169 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03654 | hp2 | a0001 | c0006 | t0005 | g0271 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03669 | hp2 | a0002 | c0004 | t0002 | g0227 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0005 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03704 | hp1 | a0001 | c0010 | t0002 | g0050 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03710 | hp1 | a0001 | c0038 | t0005 | g0176 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0042 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03831 | hp1 | a0001 | c0003 | t0002 | g0188 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03834 | hp1 | a0001 | c0042 | t0001 | g0104 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03834 | hp2 | a0001 | c0006 | t0005 | g0155 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0196 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04184 | hp1 | a0001 | c0013 | t0002 | g0003 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04199 | hp2 | a0002 | c0064 | t0002 | g0171 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04204 | hp1 | a0002 | c0004 | t0002 | g0030 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04204 | hp2 | a0023 | c0049 | t0001 | g0141 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04228 | hp1 | a0001 | c0006 | t0005 | g0074 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0198 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18522 | hp1 | a0004 | c0081 | t0006 | g0247 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18522 | hp2 | a0011 | c0027 | t0003 | g0263 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18747 | hp1 | a0006 | c0030 | t0002 | g0184 | EAS | CHB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18906 | hp1 | a0001 | c0005 | t0003 | g0014 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18906 | hp2 | a0001 | c0014 | t0001 | g0017 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18940 | hp2 | a0002 | c0004 | t0002 | g0212 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18944 | hp2 | a0001 | c0022 | t0004 | g0214 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18947 | hp2 | a0001 | c0015 | t0001 | g0122 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18948 | hp1 | a0001 | c0011 | t0001 | g0105 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18948 | hp2 | a0002 | c0060 | t0002 | g0186 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18960 | hp1 | a0001 | c0001 | t0010 | g0093 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18960 | hp2 | a0021 | c0085 | t0002 | g0223 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18963 | hp2 | a0001 | c0034 | t0004 | g0156 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18964 | hp1 | a0016 | c0076 | t0004 | g0058 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18969 | hp1 | a0007 | c0047 | t0004 | g0063 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18969 | hp2 | a0001 | c0055 | t0001 | g0082 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18975 | hp2 | a0002 | c0004 | t0002 | g0216 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18979 | hp2 | a0001 | c0022 | t0004 | g0213 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18982 | hp2 | a0001 | c0037 | t0005 | g0157 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18983 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18995 | hp2 | a0008 | c0086 | t0002 | g0220 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18998 | hp2 | a0009 | c0024 | t0001 | g0096 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19000 | hp2 | a0001 | c0011 | t0001 | g0073 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19002 | hp1 | a0007 | c0046 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19002 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19007 | hp2 | a0001 | c0023 | t0004 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19011 | hp2 | a0019 | c0044 | t0001 | g0129 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19030 | hp1 | a0001 | c0058 | t0001 | g0076 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19043 | hp1 | a0001 | c0088 | t0002 | g0237 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19043 | hp2 | a0001 | c0061 | t0017 | g0178 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19054 | hp1 | a0001 | c0041 | t0001 | g0153 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19055 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19057 | hp1 | a0001 | c0011 | t0001 | g0072 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19058 | hp1 | a0012 | c0031 | t0001 | g0103 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19058 | hp2 | a0017 | c0033 | t0009 | g0023 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19064 | hp2 | a0001 | c0035 | t0013 | g0158 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19067 | hp1 | a0014 | c0057 | t0001 | g0010 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19074 | hp2 | a0002 | c0028 | t0002 | g0218 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19083 | hp1 | a0002 | c0028 | t0002 | g0206 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19087 | hp1 | a0001 | c0023 | t0004 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19088 | hp1 | a0001 | c0001 | t0027 | g0132 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19089 | hp1 | a0002 | c0004 | t0002 | g0208 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19089 | hp2 | a0001 | c0006 | t0007 | g0024 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19240 | hp1 | a0001 | c0007 | t0001 | g0018 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19240 | hp2 | a0001 | c0069 | t0002 | g0026 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20129 | hp1 | a0001 | c0074 | t0002 | g0161 | AFR | ASW | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20129 | hp2 | a0031 | c0051 | t0001 | g0127 | AFR | ASW | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20752 | hp1 | a0001 | c0010 | t0002 | g0003 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0230 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20905 | hp1 | a0002 | c0012 | t0002 | g0228 | SAS | GIH | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20905 | hp2 | a0001 | c0003 | t0002 | g0201 | SAS | GIH | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0233 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01123 | hp2 | a0001 | c0019 | t0002 | g0172 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02109 | hp1 | a0022 | c0079 | t0001 | g0033 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02109 | hp2 | a0001 | c0014 | t0001 | g0077 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02486 | hp1 | a0001 | c0007 | t0001 | g0135 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02559 | hp1 | a0004 | c0021 | t0006 | g0246 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03471 | hp2 | a0001 | c0008 | t0003 | g0267 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG06807 | hp1 | a0004 | c0021 | t0006 | g0248 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG06807 | hp2 | a0010 | c0025 | t0002 | g0269 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18955 | hp2 | a0027 | c0050 | t0001 | g0071 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20300 | hp1 | a0003 | c0026 | t0002 | g0025 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0193 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA21309 | hp2 | a0026 | c0072 | t0002 | g0165 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
homoSapiens_chm13v2 | hp1 | a0001 | c0013 | t0002 | g0003 | REF | REF | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0023 | g0126 | REF | REF | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104868494
|
G | C | 1 | a0012 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.44G>C | p.Arg15Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/19 | 317/6727 | 44/4665 | 15/1554 | chr14 | 104868494 | ||
chr14:104880396
|
C | T | 1 | a0013 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.443C>T | p.Pro148Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/19 | 716/6727 | 443/4665 | 148/1554 | chr14 | 104880396 | ||
chr14:104883164
|
C | T | 1 | a0003 | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.707C>T | p.Pro236Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 980/6727 | 707/4665 | 236/1554 | chr14 | 104883164 | ||
chr14:104883167
|
C | T | 1 | a0006 | 2 | HG00408.hp2 NA18747.hp1 |
missense_variant | MODERATE | c.710C>T | p.Ser237Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 983/6727 | 710/4665 | 237/1554 | chr14 | 104883167 | ||
chr14:104883233
|
C | T | 1 | a0005 | 3 | HG02572.hp1 HG03579.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.776C>T | p.Ala259Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1049/6727 | 776/4665 | 259/1554 | chr14 | 104883233 | ||
chr14:104883350
|
C | T | 1 | a0014 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.893C>T | p.Pro298Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1166/6727 | 893/4665 | 298/1554 | chr14 | 104883350 | ||
chr14:104883362
|
C | T | 1 | a0032 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.905C>T | p.Ala302Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1178/6727 | 905/4665 | 302/1554 | chr14 | 104883362 | ||
chr14:104883417
|
G | C | 1 | a0015 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.960G>C | p.Gln320His | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1233/6727 | 960/4665 | 320/1554 | chr14 | 104883417 | ||
chr14:104883460
|
C | T | 1 | a0016 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.1003C>T | p.Arg335Cys | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1276/6727 | 1003/4665 | 335/1554 | chr14 | 104883460 | ||
chr14:104883885
|
C | T | 1 | a0031 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1106C>T | p.Ala369Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1379/6727 | 1106/4665 | 369/1554 | chr14 | 104883885 | ||
chr14:104884143
|
G | A | 1 | a0017 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1364G>A | p.Gly455Glu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1637/6727 | 1364/4665 | 455/1554 | chr14 | 104884143 | ||
chr14:104884218
|
C | T | 1 | a0018 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1439C>T | p.Ser480Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1712/6727 | 1439/4665 | 480/1554 | chr14 | 104884218 | ||
chr14:104884314
|
C | T | 1 | a0007 | 2 | NA18969.hp1 NA19002.hp1 |
missense_variant | MODERATE | c.1535C>T | p.Ser512Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1808/6727 | 1535/4665 | 512/1554 | chr14 | 104884314 | ||
chr14:104884322
|
G | A | 1 | a0030 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1543G>A | p.Ala515Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1816/6727 | 1543/4665 | 515/1554 | chr14 | 104884322 | ||
chr14:104884410
|
C | A | 1 | a0029 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1631C>A | p.Pro544Gln | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1904/6727 | 1631/4665 | 544/1554 | chr14 | 104884410 | ||
chr14:104885484
|
C | T | 1 | a0028 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1886C>T | p.Ala629Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/19 | 2159/6727 | 1886/4665 | 629/1554 | chr14 | 104885484 | ||
chr14:104886305
|
C | T | 1 | a0019 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.2066C>T | p.Pro689Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2339/6727 | 2066/4665 | 689/1554 | chr14 | 104886305 | ||
chr14:104886314
|
C | T | 1 | a0020 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.2075C>T | p.Ser692Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2348/6727 | 2075/4665 | 692/1554 | chr14 | 104886314 | ||
chr14:104886547
|
CGCAGGA | C | 3 | a0002a0006a0013 | 36 | HG00408.hp2 HG00544.hp1 HG01071.hp1 others(33): Show |
conservative_inframe_deletion | MODERATE | c.2311_2316delAGGAGC | p.Arg771_Ser772del | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2584/6727 | 2311/4665 | 771/1554 | INFO_REALIGN_3_PRIME | chr14 | 104886547 | |
chr14:104886580
|
A | T | 1 | a0027 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.2341A>T | p.Arg781Trp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2614/6727 | 2341/4665 | 781/1554 | chr14 | 104886580 | ||
chr14:104886607
|
G | A | 1 | a0011 | 2 | HG02055.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.2368G>A | p.Gly790Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2641/6727 | 2368/4665 | 790/1554 | chr14 | 104886607 | ||
chr14:104886674
|
C | T | 2 | a0008a0021 | 3 | HG03654.hp1 NA18960.hp2 NA18995.hp2 |
missense_variant | MODERATE | c.2435C>T | p.Pro812Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2708/6727 | 2435/4665 | 812/1554 | chr14 | 104886674 | ||
chr14:104886715
|
G | A | 1 | a0026 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2476G>A | p.Ala826Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2749/6727 | 2476/4665 | 826/1554 | chr14 | 104886715 | ||
chr14:104886799
|
C | G | 2 | a0022a0028 | 2 | HG00733.hp1 HG02109.hp1 |
missense_variant | MODERATE | c.2560C>G | p.Pro854Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2833/6727 | 2560/4665 | 854/1554 | chr14 | 104886799 | ||
chr14:104886811
|
G | A | 1 | a0010 | 2 | HG03453.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.2572G>A | p.Gly858Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2845/6727 | 2572/4665 | 858/1554 | chr14 | 104886811 | ||
chr14:104887123
|
G | A | 1 | a0009 | 2 | HG00438.hp2 NA18998.hp2 |
missense_variant | MODERATE | c.2884G>A | p.Val962Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3157/6727 | 2884/4665 | 962/1554 | chr14 | 104887123 | ||
chr14:104887141
|
A | C | 1 | a0014 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.2902A>C | p.Lys968Gln | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3175/6727 | 2902/4665 | 968/1554 | chr14 | 104887141 | ||
chr14:104887366
|
T | C | 1 | a0023 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.3127T>C | p.Trp1043Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3400/6727 | 3127/4665 | 1043/1554 | chr14 | 104887366 | ||
chr14:104887381
|
C | T | 2 | a0004a0018 | 5 | HG02559.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3142C>T | p.Arg1048Cys | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3415/6727 | 3142/4665 | 1048/1554 | chr14 | 104887381 | ||
chr14:104887449
|
C | CACCGGGG others(11): Show |
1 | a0021 | 1 | NA18960.hp2 | conservative_inframe_insertion | MODERATE | c.3211_3228dupACCGGG others(12): Show |
p.Thr1071_Leu1076dup | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3502/6727 | 3229/4665 | 1077/1554 | INFO_REALIGN_3_PRIME | chr14 | 104887449 | |
chr14:104887589
|
C | T | 1 | a0004 | 4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.3350C>T | p.Thr1117Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3623/6727 | 3350/4665 | 1117/1554 | chr14 | 104887589 | ||
chr14:104887621
|
C | T | 1 | a0025 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.3382C>T | p.Arg1128Trp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3655/6727 | 3382/4665 | 1128/1554 | chr14 | 104887621 | ||
chr14:104889696
|
T | G | 1 | a0030 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3816T>G | p.Asp1272Glu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/19 | 4089/6727 | 3816/4665 | 1272/1554 | chr14 | 104889696 | ||
chr14:104893104
|
C | T | 1 | a0024 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.4007C>T | p.Thr1336Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/19 | 4280/6727 | 4007/4665 | 1336/1554 | chr14 | 104893104 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104877887
|
G | A | 1 | a0001c0032 | 1 | HG03453.hp1 | splice_region_variant&synonymous_variant | LOW | c.198G>A | p.Thr66Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/19 | 471/6727 | 198/4665 | 66/1554 | chr14 | 104877887 | ||
chr14:104877956
|
C | T | 21 | a0001c0002a0001c0003a0001c0022others(18): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
synonymous_variant | LOW | c.267C>T | p.Phe89Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/19 | 540/6727 | 267/4665 | 89/1554 | chr14 | 104877956 | ||
chr14:104878460
|
C | T | 1 | a0003c0078 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.292C>T | p.Leu98Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/19 | 565/6727 | 292/4665 | 98/1554 | chr14 | 104878460 | ||
chr14:104878486
|
G | A | 7 | a0001c0006a0001c0034a0001c0035others(4): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
synonymous_variant | LOW | c.318G>A | p.Pro106Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/19 | 591/6727 | 318/4665 | 106/1554 | chr14 | 104878486 | ||
chr14:104880295
|
G | A | 7 | a0001c0006a0001c0034a0001c0035others(4): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
synonymous_variant | LOW | c.342G>A | p.Lys114Lys | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/19 | 615/6727 | 342/4665 | 114/1554 | chr14 | 104880295 | ||
chr14:104880392
|
A | C | 1 | a0001c0077 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.439A>C | p.Arg147Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/19 | 712/6727 | 439/4665 | 147/1554 | chr14 | 104880392 | ||
chr14:104882783
|
C | T | 1 | a0016c0076 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.528C>T | p.Asp176Asp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/19 | 801/6727 | 528/4665 | 176/1554 | chr14 | 104882783 | ||
chr14:104883051
|
A | C | 50 | a0001c0002a0001c0003a0001c0005others(47): Show | 156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
synonymous_variant | LOW | c.594A>C | p.Pro198Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 867/6727 | 594/4665 | 198/1554 | chr14 | 104883051 | ||
chr14:104883111
|
G | A | 1 | a0001c0082 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.654G>A | p.Ser218Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 927/6727 | 654/4665 | 218/1554 | chr14 | 104883111 | ||
chr14:104883135
|
C | T | 12 | a0001c0005a0001c0008a0001c0020others(9): Show | 31 | HG01167.hp2 HG01255.hp1 HG01891.hp1 others(28): Show |
synonymous_variant | LOW | c.678C>T | p.Phe226Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 951/6727 | 678/4665 | 226/1554 | chr14 | 104883135 | ||
chr14:104883270
|
C | T | 2 | a0001c0058a0001c0059 | 2 | HG02451.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.813C>T | p.Ile271Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1086/6727 | 813/4665 | 271/1554 | chr14 | 104883270 | ||
chr14:104883426
|
G | A | 2 | a0002c0028a0002c0060 | 3 | NA18948.hp2 NA19074.hp2 NA19083.hp1 |
synonymous_variant | LOW | c.969G>A | p.Pro323Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1242/6727 | 969/4665 | 323/1554 | chr14 | 104883426 | ||
chr14:104883471
|
C | T | 1 | a0001c0055 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.1014C>T | p.Thr338Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1287/6727 | 1014/4665 | 338/1554 | chr14 | 104883471 | ||
chr14:104883841
|
C | T | 16 | a0001c0003a0001c0008a0001c0010others(13): Show | 57 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(54): Show |
synonymous_variant | LOW | c.1062C>T | p.His354His | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1335/6727 | 1062/4665 | 354/1554 | chr14 | 104883841 | ||
chr14:104883898
|
T | C | 21 | a0001c0007a0001c0014a0001c0017others(18): Show | 44 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
synonymous_variant | LOW | c.1119T>C | p.Ala373Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1392/6727 | 1119/4665 | 373/1554 | chr14 | 104883898 | ||
chr14:104884018
|
A | G | 42 | a0001c0002a0001c0003a0001c0010others(39): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
synonymous_variant | LOW | c.1239A>G | p.Thr413Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1512/6727 | 1239/4665 | 413/1554 | chr14 | 104884018 | ||
chr14:104884042
|
C | G | 1 | a0001c0087 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1263C>G | p.Ser421Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1536/6727 | 1263/4665 | 421/1554 | chr14 | 104884042 | ||
chr14:104884075
|
C | T | 2 | a0001c0065a0010c0025 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.1296C>T | p.Ala432Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1569/6727 | 1296/4665 | 432/1554 | chr14 | 104884075 | ||
chr14:104884102
|
C | T | 3 | a0001c0014a0001c0048a0001c0053 | 5 | HG02109.hp2 HG02622.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.1323C>T | p.Ala441Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1596/6727 | 1323/4665 | 441/1554 | chr14 | 104884102 | ||
chr14:104884411
|
G | A | 1 | a0001c0041 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.1632G>A | p.Pro544Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1905/6727 | 1632/4665 | 544/1554 | chr14 | 104884411 | ||
chr14:104884462
|
C | T | 43 | a0001c0002a0001c0003a0001c0006others(40): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
synonymous_variant | LOW | c.1683C>T | p.Asp561Asp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1956/6727 | 1683/4665 | 561/1554 | chr14 | 104884462 | ||
chr14:104884507
|
G | A | 1 | a0001c0023 | 2 | NA19007.hp2 NA19087.hp1 |
synonymous_variant | LOW | c.1728G>A | p.Ala576Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 2001/6727 | 1728/4665 | 576/1554 | chr14 | 104884507 | ||
chr14:104884531
|
C | T | 43 | a0001c0002a0001c0003a0001c0006others(40): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
synonymous_variant | LOW | c.1752C>T | p.Ala584Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 2025/6727 | 1752/4665 | 584/1554 | chr14 | 104884531 | ||
chr14:104886054
|
G | A | 1 | a0001c0059 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1959G>A | p.Pro653Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/19 | 2232/6727 | 1959/4665 | 653/1554 | chr14 | 104886054 | ||
chr14:104886591
|
C | T | 1 | a0007c0047 | 1 | NA18969.hp1 | synonymous_variant | LOW | c.2352C>T | p.Arg784Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2625/6727 | 2352/4665 | 784/1554 | chr14 | 104886591 | ||
chr14:104886781
|
C | T | 1 | a0029c0052 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.2542C>T | p.Leu848Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2815/6727 | 2542/4665 | 848/1554 | chr14 | 104886781 | ||
chr14:104886843
|
C | T | 1 | a0001c0037 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.2604C>T | p.Ser868Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2877/6727 | 2604/4665 | 868/1554 | chr14 | 104886843 | ||
chr14:104887068
|
G | A | 2 | a0001c0017a0001c0019 | 6 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
synonymous_variant | LOW | c.2829G>A | p.Pro943Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3102/6727 | 2829/4665 | 943/1554 | chr14 | 104887068 | ||
chr14:104887644
|
A | G | 1 | a0030c0040 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3405A>G | p.Ser1135Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3678/6727 | 3405/4665 | 1135/1554 | chr14 | 104887644 | ||
chr14:104887956
|
A | G | 51 | a0001c0002a0001c0003a0001c0005others(48): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
synonymous_variant | LOW | c.3717A>G | p.Ser1239Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3990/6727 | 3717/4665 | 1239/1554 | chr14 | 104887956 | ||
chr14:104893030
|
T | C | 1 | a0001c0035 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.3933T>C | p.Asp1311Asp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/19 | 4206/6727 | 3933/4665 | 1311/1554 | chr14 | 104893030 | ||
chr14:104893790
|
G | A | 12 | a0001c0017a0001c0019a0001c0020others(9): Show | 19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
synonymous_variant | LOW | c.4212G>A | p.Pro1404Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/19 | 4485/6727 | 4212/4665 | 1404/1554 | chr14 | 104893790 | ||
chr14:104894808
|
C | G | 1 | a0001c0042 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.4515C>G | p.Arg1505Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 4788/6727 | 4515/4665 | 1505/1554 | chr14 | 104894808 | ||
chr14:104894952
|
G | C | 1 | a0001c0058 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.4659G>C | p.Leu1553Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 4932/6727 | 4659/4665 | 1553/1554 | chr14 | 104894952 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104865272
|
G | A | 1 | a0017c0033t0009 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3179 | chr14 | 104865272 | |||||
chr14:104865275
|
A | G | 1 | a0001c0001t0027 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3176 | chr14 | 104865275 | |||||
chr14:104865316
|
G | A | 1 | a0001c0001t0010 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3135 | chr14 | 104865316 | |||||
chr14:104865391
|
C | CCGGG | 6 | a0001c0001t0026a0001c0005t0003a0001c0008t0003others(3): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-135_-132dupGGCG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3041 | INFO_REALIGN_3_PRIME | chr14 | 104865391 | ||||
chr14:104865498
|
C | A | 1 | a0030c0040t0011 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 2953 | chr14 | 104865498 | |||||
chr14:104895000
|
C | G | 1 | a0001c0001t0025 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 42 | chr14 | 104895000 | |||||
chr14:104895087
|
G | A | 8 | a0001c0006t0005a0001c0006t0007a0001c0035t0013others(5): Show | 14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*129G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 129 | chr14 | 104895087 | |||||
chr14:104895100
|
G | A | 1 | a0005c0016t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*142G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 142 | chr14 | 104895100 | |||||
chr14:104895251
|
G | C | 1 | a0001c0001t0015 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 293 | chr14 | 104895251 | |||||
chr14:104895427
|
G | A | 1 | a0001c0001t0016 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 469 | chr14 | 104895427 | |||||
chr14:104895492
|
C | A | 1 | a0001c0061t0017 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 534 | chr14 | 104895492 | |||||
chr14:104895511
|
C | G | 1 | a0001c0032t0024 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 553 | chr14 | 104895511 | |||||
chr14:104895597
|
T | C | 56 | a0001c0001t0002a0001c0001t0015a0001c0002t0002others(53): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*639T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 639 | chr14 | 104895597 | |||||
chr14:104895706
|
G | A | 1 | a0001c0080t0018 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 748 | chr14 | 104895706 | |||||
chr14:104895862
|
C | T | 1 | a0001c0003t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 904 | chr14 | 104895862 | |||||
chr14:104895869
|
T | C | 1 | a0002c0009t0012 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*911T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 911 | chr14 | 104895869 | |||||
chr14:104895907
|
C | T | 8 | a0001c0001t0004a0001c0001t0016a0001c0022t0004others(5): Show | 22 | HG00673.hp1 HG01943.hp2 HG01978.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*949C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 949 | chr14 | 104895907 | |||||
chr14:104896017
|
G | A | 2 | a0004c0021t0006a0004c0081t0006 | 4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1059G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1059 | chr14 | 104896017 | |||||
chr14:104896096
|
G | A | 1 | a0001c0007t0008 | 3 | HG02055.hp2 HG02965.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1138G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1138 | chr14 | 104896096 | |||||
chr14:104896194
|
G | A | 2 | a0001c0006t0007a0024c0036t0007 | 3 | HG00438.hp1 HG01496.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1236G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1236 | chr14 | 104896194 | |||||
chr14:104896293
|
G | GC | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(102): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*1337dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1338 | INFO_REALIGN_3_PRIME | chr14 | 104896293 | ||||
chr14:104896456
|
G | A | 2 | a0001c0035t0013a0017c0033t0009 | 2 | NA19058.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1498G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1498 | chr14 | 104896456 | |||||
chr14:104896482
|
C | T | 1 | a0001c0003t0020 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1524C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1524 | chr14 | 104896482 | |||||
chr14:104896629
|
C | T | 1 | a0018c0068t0019 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1671 | chr14 | 104896629 | |||||
chr14:104896650
|
G | A | 1 | a0001c0001t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1692 | chr14 | 104896650 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104865556
|
C | T | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28+43C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865556 | ||||||
chr14:104865596
|
C | CG | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0006t0005g0036others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+87dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 104865596 | |||||
chr14:104865664
|
G | A | 42 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0040others(39): Show | 48 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.-28+151G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865664 | ||||||
chr14:104865791
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-28+278A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865791 | ||||||
chr14:104865955
|
C | T | 1 | a0001c0006t0005g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-28+442C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865955 | ||||||
chr14:104865961
|
C | T | 3 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+448C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865961 | ||||||
chr14:104866201
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18945.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-28+688T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866201 | ||||||
chr14:104866289
|
C | A | 1 | a0001c0013t0002g0037 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-28+776C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866289 | ||||||
chr14:104866338
|
C | T | 21 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-28+825C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866338 | ||||||
chr14:104866390
|
C | T | 2 | a0003c0026t0002g0250a0003c0078t0002g0249 | 2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-28+877C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866390 | ||||||
chr14:104866457
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-28+944G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866457 | ||||||
chr14:104866467
|
C | A | 3 | a0001c0011t0001g0072a0001c0011t0001g0073a0027c0050t0001g0071 | 3 | NA18955.hp2 NA19000.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-28+954C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866467 | ||||||
chr14:104866551
|
A | AG | 6 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG00140.hp1 HG01168.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+1041dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 104866551 | |||||
chr14:104866633
|
T | C | 1 | a0001c0005t0003g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-28+1120T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866633 | ||||||
chr14:104866634
|
C | G | 2 | a0010c0025t0002g0269a0010c0025t0002g0270 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+1121C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866634 | ||||||
chr14:104866806
|
C | A | 1 | a0001c0006t0005g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-28+1293C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866806 | ||||||
chr14:104866881
|
C | T | 4 | a0004c0021t0006g0245a0004c0021t0006g0246a0004c0021t0006g0248others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+1368C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866881 | ||||||
chr14:104866918
|
C | T | 1 | a0001c0003t0020g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-28+1405C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866918 | ||||||
chr14:104867202
|
A | G | 117 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(114): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-27-1222A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867202 | ||||||
chr14:104867226
|
C | T | 3 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-1198C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867226 | ||||||
chr14:104867307
|
C | T | 77 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(74): Show | 93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-27-1117C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867307 | ||||||
chr14:104867824
|
G | A | 2 | a0001c0058t0001g0076a0001c0059t0001g0075 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-27-600G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867824 | ||||||
chr14:104867859
|
C | A | 148 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(145): Show | 170 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-27-565C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867859 | ||||||
chr14:104867898
|
C | G | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27-526C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867898 | ||||||
chr14:104868092
|
C | T | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-332C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104868092 | ||||||
chr14:104868284
|
C | T | 1 | a0001c0041t0001g0153 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-27-140C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104868284 | ||||||
chr14:104868311
|
C | T | 21 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-27-113C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104868311 | ||||||
chr14:104868712
|
C | T | 77 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(74): Show | 93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.105+157C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104868712 | ||||||
chr14:104868959
|
T | C | 2 | a0001c0014t0001g0017a0001c0014t0001g0077 | 3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.105+404T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104868959 | ||||||
chr14:104869183
|
G | A | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+628G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869183 | ||||||
chr14:104869293
|
G | A | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+738G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869293 | ||||||
chr14:104869373
|
A | G | 121 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(118): Show | 139 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.105+818A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869373 | ||||||
chr14:104869520
|
C | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0151others(1): Show | 7 | NA18940.hp1 NA18945.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.105+965C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869520 | ||||||
chr14:104869541
|
T | C | 25 | a0001c0014t0001g0017a0001c0014t0001g0077a0001c0017t0002g0170others(22): Show | 26 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.105+986T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869541 | ||||||
chr14:104869797
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.105+1242A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869797 | ||||||
chr14:104869799
|
T | C | 6 | a0001c0080t0018g0078a0004c0021t0006g0245a0004c0021t0006g0246others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+1244T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869799 | ||||||
chr14:104870002
|
G | A | 1 | a0001c0020t0002g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.105+1447G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870002 | ||||||
chr14:104870063
|
G | A | 1 | a0001c0062t0002g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.105+1508G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870063 | ||||||
chr14:104870093
|
C | T | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+1538C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870093 | ||||||
chr14:104870109
|
C | CA | 116 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(113): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.105+1556dupA | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104870109 | |||||
chr14:104870210
|
G | A | 2 | a0001c0058t0001g0076a0001c0059t0001g0075 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.105+1655G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870210 | ||||||
chr14:104870227
|
C | T | 5 | a0001c0003t0002g0239a0001c0003t0002g0240a0001c0003t0002g0241others(2): Show | 5 | HG01192.hp1 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+1672C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870227 | ||||||
chr14:104870414
|
G | A | 121 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(118): Show | 139 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.105+1859G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870414 | ||||||
chr14:104870475
|
G | C | 3 | a0001c0014t0001g0017a0001c0014t0001g0077a0018c0068t0019g0080 | 4 | HG02109.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1920G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870475 | ||||||
chr14:104870478
|
C | G | 21 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.105+1923C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870478 | ||||||
chr14:104870528
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.105+1973G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870528 | ||||||
chr14:104870621
|
G | A | 1 | a0002c0004t0002g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.105+2066G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870621 | ||||||
chr14:104870645
|
G | A | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.105+2090G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870645 | ||||||
chr14:104870682
|
C | T | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2127C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870682 | ||||||
chr14:104870683
|
G | A | 1 | a0001c0071t0003g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.105+2128G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870683 | ||||||
chr14:104870847
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105+2292C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870847 | ||||||
chr14:104870913
|
G | T | 14 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0260others(11): Show | 17 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.105+2358G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870913 | ||||||
chr14:104870949
|
C | T | 22 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(19): Show | 26 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.105+2394C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870949 | ||||||
chr14:104871150
|
C | T | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+2595C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871150 | ||||||
chr14:104871176
|
G | A | 1 | a0003c0078t0002g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.105+2621G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871176 | ||||||
chr14:104871188
|
A | G | 41 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(38): Show | 42 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.105+2633A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871188 | ||||||
chr14:104871200
|
A | G | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2645A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871200 | ||||||
chr14:104871261
|
G | A | 1 | a0001c0002t0002g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.105+2706G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871261 | ||||||
chr14:104871299
|
G | A | 2 | a0001c0014t0001g0017a0001c0014t0001g0077 | 3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.105+2744G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871299 | ||||||
chr14:104871383
|
C | T | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2828C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871383 | ||||||
chr14:104871401
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.105+2846C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871401 | ||||||
chr14:104871466
|
C | T | 125 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(122): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.105+2911C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871466 | ||||||
chr14:104871760
|
G | A | 2 | a0001c0001t0001g0081a0001c0055t0001g0082 | 2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.105+3205G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871760 | ||||||
chr14:104872087
|
T | A | 1 | a0001c0002t0002g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.105+3532T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872087 | ||||||
chr14:104872121
|
C | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.105+3566C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872121 | ||||||
chr14:104872123
|
T | C | 1 | a0002c0009t0012g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.105+3568T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872123 | ||||||
chr14:104872123
|
T | TCGTGTGT others(3): Show |
1 | a0001c0007t0001g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.105+3580_105+3589d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872123 | |||||
chr14:104872143
|
GC | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0028c0045t0001g0144 | 3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.105+3590delC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872143 | |||||
chr14:104872144
|
CCGTGTGT others(14): Show |
C | 1 | a0001c0001t0001g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.105+3608_105+3628d others(23): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872144 | |||||
chr14:104872155
|
C | CCGT | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0028c0045t0001g0144 | 3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.105+3600_105+3601i others(5): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872155 | ||||||
chr14:104872187
|
T | C | 148 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(145): Show | 170 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.105+3632T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872187 | ||||||
chr14:104872191
|
T | G | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.105+3636T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872191 | ||||||
chr14:104872199
|
G | A | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.105+3644G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872199 | ||||||
chr14:104872230
|
C | T | 1 | a0020c0084t0002g0236 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.105+3675C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872230 | ||||||
chr14:104872257
|
T | G | 1 | a0001c0074t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3702T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872257 | ||||||
chr14:104872262
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0085others(7): Show | 12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+3707G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872262 | ||||||
chr14:104872265
|
T | C | 1 | a0001c0074t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3710T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872265 | ||||||
chr14:104872269
|
G | T | 1 | a0001c0074t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3714G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872269 | ||||||
chr14:104872277
|
G | A | 1 | a0001c0054t0001g0079 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.105+3722G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872277 | ||||||
chr14:104872278
|
T | C | 1 | a0001c0074t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3723T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872278 | ||||||
chr14:104872280
|
T | G | 5 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(2): Show | 5 | HG01099.hp1 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+3725T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872280 | ||||||
chr14:104872284
|
T | C | 1 | a0001c0001t0004g0015 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.105+3729T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872284 | ||||||
chr14:104872287
|
C | CGCGTGTG others(3): Show |
145 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(142): Show | 167 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.105+3735_105+3744d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872287 | |||||
chr14:104872287
|
C | T | 1 | a0001c0074t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3732C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872287 | ||||||
chr14:104872318
|
C | CCGTGGGT others(3): Show |
93 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(90): Show | 110 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.105+3778_105+3787d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872318 | |||||
chr14:104872318
|
CCGTGGGT others(13): Show |
C | 1 | a0001c0032t0024g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.105+3768_105+3787d others(22): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872318 | |||||
chr14:104872333
|
GGTGTGCG others(3): Show |
G | 24 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0070others(21): Show | 27 | HG00438.hp2 HG02135.hp1 HG02165.hp1 others(24): Show |
intron_variant | MODIFIER | c.105+3795_105+3804d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872333 | |||||
chr14:104872343
|
T | G | 47 | a0001c0001t0004g0039a0001c0001t0026g0264a0001c0005t0003g0014others(44): Show | 50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.105+3788T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872343 | ||||||
chr14:104872349
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0034t0004g0156a0001c0037t0005g0157 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.105+3795_105+3806d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872349 | ||||||
chr14:104872353
|
T | G | 1 | a0003c0026t0002g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.105+3798T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872353 | ||||||
chr14:104872357
|
T | C | 2 | a0001c0014t0001g0017a0001c0014t0001g0077 | 3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.105+3802T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872357 | ||||||
chr14:104872361
|
G | A | 1 | a0001c0088t0002g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.105+3806G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872361 | ||||||
chr14:104872362
|
CGT | C | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+3815_105+3816d others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872362 | |||||
chr14:104872364
|
T | C | 2 | a0001c0034t0004g0156a0001c0037t0005g0157 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.105+3809T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872364 | ||||||
chr14:104872364
|
TGTGTGTG others(6): Show |
T | 1 | a0001c0059t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+3815_105+3827d others(15): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872364 | |||||
chr14:104872384
|
A | G | 150 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(147): Show | 172 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.105+3829A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872384 | ||||||
chr14:104872385
|
T | TGG | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.105+3831_105+3832i others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872385 | |||||
chr14:104872401
|
G | GC | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.105+3847dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872401 | |||||
chr14:104872406
|
G | C | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3850G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872406 | ||||||
chr14:104872411
|
G | GT | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3845_106-3844i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872411 | ||||||
chr14:104872412
|
C | G | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3844C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872412 | ||||||
chr14:104872417
|
G | C | 126 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(123): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.106-3839G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872417 | ||||||
chr14:104872417
|
G | T | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3839G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872417 | ||||||
chr14:104872421
|
TGCC | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.106-3833_106-3831d others(5): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872421 | |||||
chr14:104872423
|
C | G | 2 | a0010c0025t0002g0269a0010c0025t0002g0270 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106-3833C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872423 | ||||||
chr14:104872425
|
G | A | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3831G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872425 | ||||||
chr14:104872428
|
C | T | 6 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(3): Show | 6 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-3828C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872428 | ||||||
chr14:104872434
|
T | C | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3822T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872434 | ||||||
chr14:104872435
|
G | GTGACATG others(19): Show |
1 | a0002c0060t0002g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.106-3821_106-3820i others(28): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872435 | ||||||
chr14:104872435
|
G | GTGCATGT others(18): Show |
22 | a0001c0002t0002g0005a0001c0002t0002g0027a0001c0002t0002g0182others(19): Show | 25 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.106-3821_106-3820i others(27): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872435 | ||||||
chr14:104872435
|
G | GTGCCATG others(19): Show |
53 | a0001c0002t0002g0002a0001c0002t0002g0180a0001c0002t0002g0205others(50): Show | 66 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.106-3821_106-3820i others(28): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872435 | ||||||
chr14:104872436
|
C | T | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3820C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872436 | ||||||
chr14:104872436
|
CGT | C | 24 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(21): Show | 28 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.106-3812_106-3811d others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872436 | |||||
chr14:104872440
|
T | G | 3 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154 | 3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3816T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872440 | ||||||
chr14:104872448
|
A | G | 5 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(2): Show | 5 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3808A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872448 | ||||||
chr14:104872459
|
TGTGG | T | 5 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(2): Show | 5 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3793_106-3790d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872459 | |||||
chr14:104872470
|
CGT | C | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.106-3778_106-3777d others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872470 | |||||
chr14:104872478
|
T | C | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-3778T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872478 | ||||||
chr14:104872479
|
G | GC | 5 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(2): Show | 5 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3776dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872479 | |||||
chr14:104872479
|
G | GCGTGTGT others(13): Show |
58 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(55): Show | 64 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.106-3758_106-3757i others(22): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872479 | |||||
chr14:104872479
|
G | GTGTGTGC others(11): Show |
1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-3777_106-3776i others(20): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872479 | ||||||
chr14:104872489
|
CGTGT | C | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.106-3759_106-3756d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872489 | |||||
chr14:104872552
|
C | T | 1 | a0001c0015t0001g0064 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.106-3704C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872552 | ||||||
chr14:104872559
|
T | TC | 3 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106-3697_106-3696i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872559 | ||||||
chr14:104872581
|
C | G | 1 | a0001c0007t0008g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.106-3675C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872581 | ||||||
chr14:104872605
|
G | A | 1 | a0001c0013t0002g0037 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.106-3651G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872605 | ||||||
chr14:104872661
|
G | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0028c0045t0001g0144 | 3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106-3595G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872661 | ||||||
chr14:104872690
|
C | T | 1 | a0001c0003t0002g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.106-3566C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872690 | ||||||
chr14:104872691
|
G | A | 1 | a0001c0003t0002g0187 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.106-3565G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872691 | ||||||
chr14:104872717
|
G | A | 6 | a0001c0006t0005g0023a0001c0006t0007g0024a0001c0035t0013g0158others(3): Show | 7 | HG00438.hp1 HG01496.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-3539G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872717 | ||||||
chr14:104872821
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.106-3435C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872821 | ||||||
chr14:104872836
|
C | G | 1 | a0001c0032t0024g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.106-3420C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872836 | ||||||
chr14:104872911
|
G | A | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-3345G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872911 | ||||||
chr14:104872947
|
T | C | 69 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(66): Show | 85 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.106-3309T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872947 | ||||||
chr14:104873223
|
G | C | 73 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.106-3033G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873223 | ||||||
chr14:104873310
|
A | G | 21 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.106-2946A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873310 | ||||||
chr14:104873331
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.106-2925G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873331 | ||||||
chr14:104873442
|
T | C | 2 | a0001c0058t0001g0076a0001c0059t0001g0075 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.106-2814T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873442 | ||||||
chr14:104873631
|
T | C | 97 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(94): Show | 114 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.106-2625T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873631 | ||||||
chr14:104873647
|
G | A | 1 | a0020c0084t0002g0236 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.106-2609G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873647 | ||||||
chr14:104873675
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106-2581C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873675 | ||||||
chr14:104873676
|
G | T | 1 | a0001c0001t0022g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-2580G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873676 | ||||||
chr14:104873786
|
C | T | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-2470C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873786 | ||||||
chr14:104873793
|
C | T | 127 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(124): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.106-2463C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873793 | ||||||
chr14:104873841
|
G | C | 1 | a0001c0011t0001g0105 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.106-2415G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873841 | ||||||
chr14:104874033
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0152 | 5 | NA18940.hp1 NA18947.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-2223C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874033 | ||||||
chr14:104874173
|
C | T | 7 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0142others(4): Show | 7 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-2083C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874173 | ||||||
chr14:104874234
|
C | T | 2 | a0001c0014t0001g0017a0001c0014t0001g0077 | 3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.106-2022C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874234 | ||||||
chr14:104874306
|
C | T | 148 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(145): Show | 170 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.106-1950C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874306 | ||||||
chr14:104874656
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.106-1600A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874656 | ||||||
chr14:104874661
|
C | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0028c0045t0001g0144 | 3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106-1595C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874661 | ||||||
chr14:104874713
|
C | A | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-1543C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874713 | ||||||
chr14:104874763
|
T | A | 141 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(138): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.106-1493T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874763 | ||||||
chr14:104874773
|
A | C | 141 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(138): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.106-1483A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874773 | ||||||
chr14:104874940
|
A | G | 7 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0142others(4): Show | 7 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-1316A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874940 | ||||||
chr14:104875165
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.106-1091C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875165 | ||||||
chr14:104875221
|
G | A | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-1035G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875221 | ||||||
chr14:104875391
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.106-865G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875391 | ||||||
chr14:104875464
|
C | G | 1 | a0001c0005t0003g0255 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.106-792C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875464 | ||||||
chr14:104875514
|
G | A | 1 | a0001c0054t0001g0079 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.106-742G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875514 | ||||||
chr14:104875529
|
G | A | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-727G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875529 | ||||||
chr14:104875559
|
C | T | 4 | a0001c0002t0002g0194a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG02015.hp1 HG02129.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-697C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875559 | ||||||
chr14:104875560
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.106-696G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875560 | ||||||
chr14:104875621
|
T | C | 21 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.106-635T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875621 | ||||||
chr14:104875631
|
G | A | 2 | a0015c0039t0001g0106a0025c0043t0001g0102 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.106-625G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875631 | ||||||
chr14:104875654
|
C | T | 2 | a0003c0026t0002g0250a0003c0078t0002g0249 | 2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.106-602C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875654 | ||||||
chr14:104875924
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.106-332G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875924 | ||||||
chr14:104876010
|
G | A | 2 | a0001c0014t0001g0017a0001c0014t0001g0077 | 3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.106-246G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104876010 | ||||||
chr14:104876170
|
G | T | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-86G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104876170 | ||||||
chr14:104876500
|
C | T | 2 | a0001c0001t0002g0243a0001c0011t0001g0133 | 2 | HG01361.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.195+155C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876500 | ||||||
chr14:104876509
|
A | T | 77 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(74): Show | 93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+164A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876509 | ||||||
chr14:104876538
|
T | C | 45 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(42): Show | 50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+193T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876538 | ||||||
chr14:104876583
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.195+238C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876583 | ||||||
chr14:104876644
|
C | G | 77 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(74): Show | 93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+299C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876644 | ||||||
chr14:104876645
|
A | G | 77 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(74): Show | 93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+300A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876645 | ||||||
chr14:104876707
|
G | C | 4 | a0004c0021t0006g0245a0004c0021t0006g0246a0004c0021t0006g0248others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+362G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876707 | ||||||
chr14:104876708
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.195+363C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876708 | ||||||
chr14:104876769
|
C | T | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+424C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876769 | ||||||
chr14:104877035
|
G | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0142others(1): Show | 4 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+690G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877035 | ||||||
chr14:104877057
|
ACT | A | 45 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(42): Show | 50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+715_195+716del others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877057 | |||||
chr14:104877182
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.196-703G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877182 | ||||||
chr14:104877190
|
C | A | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-695C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877190 | ||||||
chr14:104877256
|
A | G | 90 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(87): Show | 107 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.196-629A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877256 | ||||||
chr14:104877349
|
G | A | 24 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(21): Show | 25 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.196-536G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877349 | ||||||
chr14:104877410
|
G | T | 1 | a0001c0041t0001g0153 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.196-475G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877410 | ||||||
chr14:104877447
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0022g0090others(2): Show | 6 | HG01891.hp2 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-438G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877447 | ||||||
chr14:104877512
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196-373C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877512 | ||||||
chr14:104877774
|
G | A | 75 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(72): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.196-111G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877774 | ||||||
chr14:104877805
|
G | A | 45 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(42): Show | 50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.196-80G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877805 | ||||||
chr14:104877820
|
G | A | 75 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(72): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.196-65G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877820 | ||||||
chr14:104877845
|
C | T | 29 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0040others(26): Show | 33 | HG00140.hp1 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.196-40C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877845 | ||||||
chr14:104877851
|
T | TC | 87 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0020others(84): Show | 99 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.196-20dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | |||||
chr14:104877851
|
T | TCC | 27 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0019others(24): Show | 32 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-21_196-20dupCC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | |||||
chr14:104877851
|
TC | T | 19 | a0001c0001t0001g0046a0001c0001t0001g0089a0001c0001t0027g0132others(16): Show | 20 | HG00438.hp1 HG01069.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-20delC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | |||||
chr14:104877851
|
TCCC | T | 16 | a0001c0003t0002g0188a0001c0003t0002g0198a0001c0006t0005g0036others(13): Show | 16 | HG01099.hp1 HG01261.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.196-22_196-20delCC others(1): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | |||||
chr14:104877851
|
TCCCC | T | 68 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(65): Show | 84 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.196-23_196-20delCC others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | |||||
chr14:104877858
|
C | G | 1 | a0001c0007t0001g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.196-27C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877858 | ||||||
chr14:104877981
|
G | A | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+18G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104877981 | ||||||
chr14:104878010
|
C | G | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+47C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878010 | ||||||
chr14:104878082
|
A | G | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+119A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878082 | ||||||
chr14:104878141
|
C | T | 1 | a0002c0060t0002g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.274+178C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878141 | ||||||
chr14:104878176
|
G | A | 1 | a0001c0020t0002g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.274+213G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878176 | ||||||
chr14:104878196
|
C | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+233C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878196 | ||||||
chr14:104878231
|
C | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.275-212C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878231 | ||||||
chr14:104878254
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0089 | 3 | HG02970.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.275-189C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878254 | ||||||
chr14:104878266
|
C | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.275-177C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878266 | ||||||
chr14:104878402
|
C | T | 2 | a0002c0004t0002g0227a0002c0012t0002g0228 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.275-41C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878402 | ||||||
chr14:104878424
|
C | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.275-19C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878424 | ||||||
chr14:104878535
|
C | T | 48 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(45): Show | 55 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.333+34C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878535 | ||||||
chr14:104878536
|
G | A | 1 | a0001c0007t0008g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+35G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878536 | ||||||
chr14:104878546
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.333+45C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878546 | ||||||
chr14:104878609
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(1): Show | 4 | NA19000.hp1 NA19007.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+108G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878609 | ||||||
chr14:104878698
|
C | A | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.333+197C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878698 | ||||||
chr14:104878722
|
A | ACAGGTGG others(16): Show |
13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+223_333+245dup others(23): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 104878722 | |||||
chr14:104878731
|
G | A | 21 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(18): Show | 21 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+230G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878731 | ||||||
chr14:104878745
|
G | A | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333+244G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878745 | ||||||
chr14:104878787
|
G | A | 1 | a0026c0072t0002g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.333+286G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878787 | ||||||
chr14:104878806
|
G | T | 1 | a0001c0053t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.333+305G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878806 | ||||||
chr14:104878870
|
A | G | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+369A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878870 | ||||||
chr14:104878896
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.333+395G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878896 | ||||||
chr14:104878939
|
G | A | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333+438G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878939 | ||||||
chr14:104878975
|
C | T | 21 | a0001c0001t0026g0264a0001c0005t0003g0014a0001c0005t0003g0032others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+474C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878975 | ||||||
chr14:104878994
|
T | C | 140 | a0001c0001t0026g0264a0001c0002t0002g0002a0001c0002t0002g0005others(137): Show | 162 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.333+493T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878994 | ||||||
chr14:104879102
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0142 | 3 | HG00639.hp1 HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.333+601G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879102 | ||||||
chr14:104879198
|
G | A | 1 | a0001c0038t0005g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333+697G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879198 | ||||||
chr14:104879271
|
G | A | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+770G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879271 | ||||||
chr14:104879444
|
G | A | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-843G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879444 | ||||||
chr14:104879461
|
G | A | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-826G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879461 | ||||||
chr14:104879469
|
A | G | 1 | a0011c0027t0003g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334-818A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879469 | ||||||
chr14:104879753
|
C | T | 1 | a0022c0079t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.334-534C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879753 | ||||||
chr14:104879796
|
A | G | 273 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(270): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.334-491A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879796 | ||||||
chr14:104879818
|
A | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0005t0003g0255others(3): Show | 6 | HG01099.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-469A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879818 | ||||||
chr14:104879865
|
C | T | 1 | a0001c0059t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.334-422C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879865 | ||||||
chr14:104879866
|
G | A | 18 | a0001c0006t0005g0023a0001c0006t0005g0154a0001c0006t0005g0271others(15): Show | 19 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.334-421G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879866 | ||||||
chr14:104879887
|
C | T | 1 | a0002c0004t0002g0203 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.334-400C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879887 | ||||||
chr14:104879903
|
C | T | 94 | a0001c0002t0002g0002a0001c0002t0002g0027a0001c0002t0002g0202others(91): Show | 111 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.334-384C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879903 | ||||||
chr14:104879946
|
G | T | 24 | a0001c0003t0002g0225a0001c0005t0003g0032a0001c0005t0003g0251others(21): Show | 27 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.334-341G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879946 | ||||||
chr14:104880108
|
G | A | 2 | a0001c0001t0004g0054a0002c0012t0002g0211 | 2 | HG02735.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.334-179G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104880108 | ||||||
chr14:104880112
|
C | T | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-175C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104880112 | ||||||
chr14:104880485
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0131 | 2 | NA19063.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.472+60C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880485 | ||||||
chr14:104880490
|
C | T | 1 | a0002c0028t0002g0218 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.472+65C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880490 | ||||||
chr14:104880532
|
G | A | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.472+107G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880532 | ||||||
chr14:104880570
|
T | C | 134 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(131): Show | 155 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.472+145T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880570 | ||||||
chr14:104880597
|
T | C | 1 | a0001c0002t0002g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.472+172T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880597 | ||||||
chr14:104880688
|
C | G | 4 | a0001c0005t0003g0251a0001c0005t0003g0253a0001c0005t0003g0254others(1): Show | 4 | HG01255.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+263C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880688 | ||||||
chr14:104880693
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.472+268A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880693 | ||||||
chr14:104880808
|
A | C | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.472+383A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880808 | ||||||
chr14:104880898
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.472+473A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880898 | ||||||
chr14:104880911
|
C | G | 54 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(51): Show | 57 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.472+486C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880911 | ||||||
chr14:104880959
|
G | A | 14 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(11): Show | 15 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+534G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880959 | ||||||
chr14:104881021
|
G | A | 2 | a0001c0058t0001g0076a0001c0059t0001g0075 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+596G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881021 | ||||||
chr14:104881085
|
G | T | 1 | a0001c0002t0002g0224 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.472+660G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881085 | ||||||
chr14:104881103
|
G | A | 1 | a0001c0003t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.472+678G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881103 | ||||||
chr14:104881151
|
C | T | 114 | a0001c0001t0001g0034a0001c0001t0001g0120a0001c0001t0001g0121others(111): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.472+726C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881151 | ||||||
chr14:104881197
|
G | C | 1 | a0001c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.472+772G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881197 | ||||||
chr14:104881351
|
G | A | 11 | a0001c0003t0002g0221a0001c0006t0005g0023a0001c0006t0005g0036others(8): Show | 11 | HG01099.hp1 HG01109.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.472+926G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881351 | ||||||
chr14:104881627
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.473-1101G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881627 | ||||||
chr14:104881658
|
G | C | 1 | a0001c0011t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.473-1070G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881658 | ||||||
chr14:104881676
|
G | A | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.473-1052G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881676 | ||||||
chr14:104881681
|
A | C | 2 | a0001c0034t0004g0156a0001c0037t0005g0157 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.473-1047A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881681 | ||||||
chr14:104881681
|
A | G | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.473-1047A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881681 | ||||||
chr14:104881684
|
G | A | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.473-1044G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881684 | ||||||
chr14:104881702
|
G | A | 75 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(72): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.473-1026G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881702 | ||||||
chr14:104881714
|
A | G | 142 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(139): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.473-1014A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881714 | ||||||
chr14:104881823
|
G | A | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 12 | HG01099.hp1 HG01516.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.473-905G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881823 | ||||||
chr14:104881884
|
G | C | 1 | a0002c0009t0002g0215 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.473-844G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881884 | ||||||
chr14:104881910
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.473-818A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881910 | ||||||
chr14:104881934
|
C | T | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-794C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881934 | ||||||
chr14:104881997
|
C | T | 19 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(16): Show | 19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.473-731C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881997 | ||||||
chr14:104882001
|
C | G | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-727C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882001 | ||||||
chr14:104882038
|
A | C | 2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.473-690A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882038 | ||||||
chr14:104882161
|
T | C | 21 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.473-567T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882161 | ||||||
chr14:104882188
|
G | T | 1 | a0002c0004t0002g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.473-540G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882188 | ||||||
chr14:104882215
|
C | T | 97 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(94): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.473-513C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882215 | ||||||
chr14:104882225
|
A | G | 21 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.473-503A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882225 | ||||||
chr14:104882227
|
GT | G | 21 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.473-500delT | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882227 | ||||||
chr14:104882379
|
T | G | 2 | a0003c0026t0002g0025a0003c0067t0002g0025 | 2 | HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.473-349T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882379 | ||||||
chr14:104882387
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.473-341G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882387 | ||||||
chr14:104882396
|
G | T | 105 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(102): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.473-332G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882396 | ||||||
chr14:104882433
|
A | G | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-295A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882433 | ||||||
chr14:104882435
|
A | G | 1 | a0002c0029t0002g0031 | 2 | HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.473-293A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882435 | ||||||
chr14:104882447
|
AGAGGAGG others(11): Show |
A | 2 | a0001c0061t0017g0178a0001c0062t0002g0177 | 2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.473-262_473-245del others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 104882447 | |||||
chr14:104882466
|
GAGGAGGG others(11): Show |
G | 3 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.473-258_473-241del others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 104882466 | |||||
chr14:104882513
|
G | C | 1 | a0001c0001t0004g0060 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.473-215G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882513 | ||||||
chr14:104882849
|
G | C | 3 | a0001c0019t0002g0167a0001c0019t0002g0168a0001c0019t0002g0172 | 3 | HG00733.hp2 HG01123.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.577+17G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/18 | chr14 | 104882849 | ||||||
chr14:104882883
|
T | G | 135 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(132): Show | 156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.577+51T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/18 | chr14 | 104882883 | ||||||
chr14:104882933
|
G | A | 1 | a0001c0032t0024g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.577+101G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/18 | chr14 | 104882933 | ||||||
chr14:104883529
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1051+21C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883529 | ||||||
chr14:104883540
|
C | T | 127 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(124): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1051+32C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883540 | ||||||
chr14:104883549
|
C | T | 131 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(128): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1051+41C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883549 | ||||||
chr14:104883554
|
G | A | 76 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(73): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1051+46G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883554 | ||||||
chr14:104883560
|
A | G | 132 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(129): Show | 153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1051+52A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883560 | ||||||
chr14:104883683
|
G | A | 2 | a0001c0002t0002g0182a0001c0003t0002g0190 | 2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1052-148G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883683 | ||||||
chr14:104883709
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1052-122G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883709 | ||||||
chr14:104883712
|
C | G | 1 | a0022c0079t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1052-119C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883712 | ||||||
chr14:104883796
|
C | T | 5 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(2): Show | 5 | HG01099.hp1 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-35C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883796 | ||||||
chr14:104884561
|
C | CGGCGAGT others(354): Show |
1 | a0001c0022t0004g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1770+204_1770+205i others(363): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884561 | |||||
chr14:104884561
|
CGGCGAGT others(45): Show |
C | 1 | a0016c0076t0004g0058 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1770+45_1770+96del others(52): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884561 | |||||
chr14:104884576
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1770+27C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884576 | ||||||
chr14:104884579
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0070others(20): Show | 25 | HG00438.hp2 HG00673.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.1770+30G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884579 | ||||||
chr14:104884587
|
CG | C | 23 | a0001c0001t0001g0109a0001c0005t0003g0014a0001c0005t0003g0032others(20): Show | 27 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1770+45delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884587 | |||||
chr14:104884588
|
G | GGGGGGGT others(44): Show |
9 | a0001c0002t0002g0197a0001c0020t0002g0026a0001c0020t0002g0160others(6): Show | 9 | HG02129.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1770+103_1770+153d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884588 | |||||
chr14:104884588
|
G | GGGGGGGT others(96): Show |
1 | a0003c0026t0002g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1770+96_1770+97ins others(103): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884588 | |||||
chr14:104884593
|
G | A | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1770+44G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884593 | ||||||
chr14:104884601
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1770+52C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884601 | ||||||
chr14:104884607
|
C | CG | 5 | a0001c0001t0001g0149a0001c0008t0003g0265a0009c0024t0001g0096others(2): Show | 5 | HG02055.hp1 HG03486.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+63dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884607 | |||||
chr14:104884652
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1770+103C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884652 | ||||||
chr14:104884652
|
CGATGCCG others(199): Show |
C | 12 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0035others(9): Show | 15 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1770+180_1770+385d others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884652 | |||||
chr14:104884653
|
G | A | 1 | a0003c0026t0002g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1770+104G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884653 | ||||||
chr14:104884653
|
G | GATGCCGG others(44): Show |
5 | a0001c0017t0002g0173a0001c0017t0002g0174a0001c0019t0002g0167others(2): Show | 5 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+153_1770+154i others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884653 | |||||
chr14:104884669
|
A | G | 1 | a0001c0070t0001g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1770+120A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884669 | ||||||
chr14:104884690
|
CGGGGGGT others(96): Show |
C | 18 | a0001c0002t0002g0002a0001c0002t0002g0205a0001c0002t0002g0224others(15): Show | 23 | HG00140.hp2 HG00438.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1770+193_1770+295d others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884690 | |||||
chr14:104884690
|
CGGGGGGT others(148): Show |
C | 2 | a0001c0003t0002g0193a0001c0003t0002g0201 | 2 | NA20905.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1770+193_1770+347d others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884690 | |||||
chr14:104884691
|
G | C | 6 | a0001c0001t0001g0109a0001c0003t0002g0232a0001c0003t0002g0235others(3): Show | 6 | HG01109.hp2 HG01192.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1770+142G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884691 | ||||||
chr14:104884691
|
GGGGGGTG others(44): Show |
G | 4 | a0001c0082t0002g0200a0002c0028t0002g0206a0002c0064t0002g0171others(1): Show | 4 | HG02698.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+193_1770+243d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884691 | |||||
chr14:104884703
|
T | C | 95 | a0001c0002t0002g0005a0001c0002t0002g0027a0001c0002t0002g0180others(92): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1770+154T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884703 | ||||||
chr14:104884703
|
T | TGATGCCG others(44): Show |
1 | a0001c0001t0001g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1770+192_1770+193i others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884703 | |||||
chr14:104884703
|
T | TGATGCCG others(180): Show |
1 | a0001c0003t0002g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1770+192_1770+193i others(189): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884703 | |||||
chr14:104884703
|
T | TGATGCCG others(179): Show |
4 | a0001c0003t0002g0235a0001c0003t0002g0239a0001c0003t0002g0240others(1): Show | 4 | HG01192.hp1 HG01928.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+192_1770+193i others(188): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884703 | |||||
chr14:104884718
|
C | T | 1 | a0007c0047t0004g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1770+169C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884718 | ||||||
chr14:104884729
|
C | A | 1 | a0020c0084t0002g0236 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1770+180C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884729 | ||||||
chr14:104884741
|
C | CG | 4 | a0001c0003t0002g0191a0001c0074t0002g0161a0001c0087t0002g0209others(1): Show | 4 | HG01175.hp1 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1770+192_1770+193i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | ||||||
chr14:104884741
|
C | CGGGGGGG others(148): Show |
1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1770+192_1770+193i others(157): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | ||||||
chr14:104884741
|
C | CGGGGGGT others(147): Show |
1 | a0003c0078t0002g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1770+192_1770+193i others(156): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | ||||||
chr14:104884741
|
C | CGGGGGGT others(199): Show |
2 | a0003c0026t0002g0025a0003c0067t0002g0025 | 2 | HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1770+192_1770+193i others(208): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | ||||||
chr14:104884741
|
CCGGGGGT others(45): Show |
C | 46 | a0001c0002t0002g0005a0001c0002t0002g0180a0001c0002t0002g0182others(43): Show | 58 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1770+193_1770+244d others(54): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | ||||||
chr14:104884742
|
C | CGGGGGTG others(96): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(2): Show | 5 | HG02559.hp2 HG02683.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1770+199_1770+301d others(105): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884742 | |||||
chr14:104884742
|
C | G | 32 | a0001c0001t0001g0109a0001c0002t0002g0027a0001c0002t0002g0192others(29): Show | 34 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1770+193C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884742 | ||||||
chr14:104884742
|
CGGGGGTG others(45): Show |
C | 15 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0089others(12): Show | 17 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1770+302_1770+353d others(54): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884742 | |||||
chr14:104884754
|
T | C | 29 | a0001c0002t0002g0027a0001c0002t0002g0192a0001c0002t0002g0202others(26): Show | 31 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1770+205T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884754 | ||||||
chr14:104884780
|
C | A | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1770+231C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884780 | ||||||
chr14:104884792
|
C | CCGGGGGT others(95): Show |
1 | a0002c0012t0002g0029 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1770+243_1770+244i others(104): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884792 | ||||||
chr14:104884792
|
CG | C | 29 | a0001c0003t0002g0204a0001c0003t0002g0225a0001c0003t0002g0232others(26): Show | 31 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1770+250delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884792 | |||||
chr14:104884793
|
G | C | 1 | a0002c0012t0002g0029 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1770+244G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884793 | ||||||
chr14:104884793
|
G | GGGGGGGT others(44): Show |
14 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(11): Show | 14 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1770+251_1770+301d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | |||||
chr14:104884793
|
G | GGGGGGTG others(94): Show |
1 | a0002c0012t0002g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1770+249_1770+250i others(103): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | |||||
chr14:104884793
|
G | GGGGGGTG others(504): Show |
1 | a0001c0003t0002g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1770+249_1770+250i others(513): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | |||||
chr14:104884793
|
G | GGGGGGTG others(351): Show |
1 | a0001c0087t0002g0209 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1770+249_1770+250i others(360): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | |||||
chr14:104884794
|
G | C | 9 | a0001c0015t0001g0108a0001c0061t0017g0178a0001c0062t0002g0177others(6): Show | 9 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1770+245G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884794 | ||||||
chr14:104884794
|
G | GGGGGTGG others(94): Show |
1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1770+249_1770+250i others(103): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884794 | |||||
chr14:104884795
|
G | T | 1 | a0007c0047t0004g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1770+246G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884795 | ||||||
chr14:104884806
|
T | C | 79 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0180others(76): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1770+257T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884806 | ||||||
chr14:104884806
|
T | TGATGCCG others(197): Show |
1 | a0006c0030t0002g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1770+301_1770+302i others(206): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884806 | |||||
chr14:104884806
|
T | TGATGCCG others(146): Show |
1 | a0001c0010t0002g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1770+301_1770+302i others(155): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884806 | |||||
chr14:104884812
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1770+263C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884812 | ||||||
chr14:104884813
|
GGGGGTGG others(44): Show |
G | 1 | a0001c0002t0002g0192 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1770+269_1770+319d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884813 | |||||
chr14:104884832
|
C | A | 2 | a0002c0004t0002g0179a0002c0004t0002g0181 | 2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1770+283C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884832 | ||||||
chr14:104884844
|
C | T | 1 | a0001c0032t0024g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1770+295C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884844 | ||||||
chr14:104884844
|
CG | C | 19 | a0001c0002t0002g0027a0001c0002t0002g0202a0001c0002t0002g0231others(16): Show | 23 | HG00642.hp1 HG00733.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1770+302delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884844 | |||||
chr14:104884845
|
G | GGGGGGGT others(95): Show |
1 | a0001c0003t0002g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1770+308_1770+309i others(104): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884845 | |||||
chr14:104884845
|
G | GGGGGGTG others(43): Show |
1 | a0001c0032t0024g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1770+301_1770+302i others(52): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884845 | |||||
chr14:104884845
|
G | GGGGGGTG others(455): Show |
1 | a0001c0083t0002g0226 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1770+301_1770+302i others(464): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884845 | |||||
chr14:104884858
|
T | C | 10 | a0001c0003t0002g0193a0001c0003t0002g0201a0001c0003t0002g0204others(7): Show | 10 | HG01081.hp1 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1770+309T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884858 | ||||||
chr14:104884884
|
C | A | 4 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270others(1): Show | 4 | HG00733.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+335C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884884 | ||||||
chr14:104884896
|
C | CGGGGGGG others(45): Show |
1 | a0001c0001t0001g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1770+302_1770+353d others(54): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884896 | |||||
chr14:104884896
|
C | CGGGGGGG others(97): Show |
1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1770+250_1770+353d others(106): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884896 | |||||
chr14:104884896
|
C | CGGGGGGT others(96): Show |
1 | a0001c0015t0001g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1770+385_1770+386i others(105): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884896 | |||||
chr14:104884896
|
C | T | 20 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(17): Show | 20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770+347C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884896 | ||||||
chr14:104884897
|
G | C | 2 | a0001c0083t0002g0226a0018c0068t0019g0080 | 2 | HG01099.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1770+348G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884897 | ||||||
chr14:104884897
|
G | GGGGGGGT others(249): Show |
4 | a0001c0005t0003g0032a0001c0005t0003g0257a0001c0005t0003g0260others(1): Show | 5 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+353_1770+354i others(258): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884897 | |||||
chr14:104884897
|
G | GGGGGGGT others(402): Show |
1 | a0001c0005t0003g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1770+353_1770+354i others(411): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884897 | |||||
chr14:104884897
|
G | GGGGGGGT others(352): Show |
4 | a0001c0008t0003g0261a0001c0008t0003g0262a0001c0018t0003g0013others(1): Show | 6 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1770+353_1770+354i others(361): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884897 | |||||
chr14:104884902
|
G | A | 1 | a0001c0032t0024g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1770+353G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884902 | ||||||
chr14:104884909
|
T | C | 19 | a0001c0003t0002g0193a0001c0003t0002g0201a0001c0003t0002g0204others(16): Show | 22 | HG00733.hp1 HG01081.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1770+360T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884909 | ||||||
chr14:104884909
|
T | TGATGCCG others(301): Show |
1 | a0001c0008t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1770+371_1770+372i others(310): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | |||||
chr14:104884909
|
T | TGATGCCG others(303): Show |
1 | a0011c0027t0003g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1770+385_1770+386i others(312): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | |||||
chr14:104884909
|
T | TGATGCCG others(300): Show |
10 | a0001c0005t0003g0014a0001c0005t0003g0251a0001c0005t0003g0253others(7): Show | 11 | HG01255.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1770+385_1770+386i others(309): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | |||||
chr14:104884909
|
T | TGATGCCG others(197): Show |
1 | a0004c0021t0006g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1770+385_1770+386i others(206): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | |||||
chr14:104884934
|
C | T | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1770+385C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884934 | ||||||
chr14:104884935
|
A | C | 9 | a0001c0001t0027g0132a0001c0002t0002g0027a0001c0002t0002g0202others(6): Show | 10 | HG00733.hp1 HG01257.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1770+386A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884935 | ||||||
chr14:104884947
|
C | T | 2 | a0001c0058t0001g0076a0028c0045t0001g0144 | 2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1770+398C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884947 | ||||||
chr14:104884948
|
G | C | 1 | a0028c0045t0001g0144 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1770+399G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884948 | ||||||
chr14:104884955
|
G | A | 1 | a0001c0005t0003g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1770+406G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884955 | ||||||
chr14:104884960
|
C | T | 2 | a0001c0015t0001g0108a0018c0068t0019g0080 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-409C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884960 | ||||||
chr14:104884967
|
G | A | 2 | a0001c0054t0001g0079a0029c0052t0001g0047 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1771-402G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884967 | ||||||
chr14:104884975
|
C | T | 2 | a0001c0001t0004g0008a0001c0023t0004g0008 | 3 | NA19007.hp2 NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1771-394C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884975 | ||||||
chr14:104884985
|
C | T | 1 | a0028c0045t0001g0144 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1771-384C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884985 | ||||||
chr14:104884986
|
C | A | 2 | a0018c0068t0019g0080a0028c0045t0001g0144 | 2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-383C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884986 | ||||||
chr14:104884998
|
T | C | 2 | a0018c0068t0019g0080a0028c0045t0001g0144 | 2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-371T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884998 | ||||||
chr14:104884999
|
C | G | 2 | a0018c0068t0019g0080a0028c0045t0001g0144 | 2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-370C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884999 | ||||||
chr14:104885004
|
G | A | 1 | a0001c0058t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1771-365G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885004 | ||||||
chr14:104885005
|
T | G | 1 | a0001c0015t0001g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1771-364T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885005 | ||||||
chr14:104885018
|
G | A | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1771-351G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885018 | ||||||
chr14:104885030
|
T | A | 1 | a0001c0007t0001g0018 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1771-339T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885030 | ||||||
chr14:104885036
|
T | C | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1771-333T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885036 | ||||||
chr14:104885049
|
C | CG | 8 | a0001c0001t0001g0125a0001c0003t0002g0187a0001c0003t0002g0232others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1771-314dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104885049 | |||||
chr14:104885103
|
G | C | 120 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(117): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1771-266G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885103 | ||||||
chr14:104885242
|
G | A | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1771-127G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885242 | ||||||
chr14:104885267
|
G | A | 1 | a0001c0066t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1771-102G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885267 | ||||||
chr14:104885300
|
A | G | 142 | a0001c0001t0001g0066a0001c0002t0002g0002a0001c0002t0002g0005others(139): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1771-69A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885300 | ||||||
chr14:104885313
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1771-56G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885313 | ||||||
chr14:104885336
|
C | T | 119 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(116): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1771-33C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885336 | ||||||
chr14:104885731
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1944+189T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885731 | ||||||
chr14:104885781
|
C | T | 9 | a0001c0014t0001g0017a0001c0014t0001g0077a0001c0070t0001g0166others(6): Show | 10 | HG00733.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1944+239C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885781 | ||||||
chr14:104885841
|
G | A | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945-199G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885841 | ||||||
chr14:104885867
|
T | C | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0094others(6): Show | 9 | NA18952.hp2 NA18960.hp1 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1945-173T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885867 | ||||||
chr14:104885918
|
T | A | 140 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(137): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1945-122T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885918 | ||||||
chr14:104886196
|
G | A | 1 | a0001c0003t0002g0242 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2035+66G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/18 | chr14 | 104886196 | ||||||
chr14:104886199
|
C | T | 12 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(9): Show | 13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035+69C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/18 | chr14 | 104886199 | ||||||
chr14:104886246
|
C | T | 3 | a0001c0005t0003g0032a0001c0005t0003g0256a0001c0005t0003g0257 | 4 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2036-29C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/18 | chr14 | 104886246 | ||||||
chr14:104888023
|
C | G | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3739+45C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888023 | ||||||
chr14:104888138
|
T | A | 1 | a0001c0001t0015g0042 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3739+160T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888138 | ||||||
chr14:104888151
|
G | A | 1 | a0022c0079t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3739+173G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888151 | ||||||
chr14:104888161
|
C | T | 20 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(17): Show | 20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3739+183C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888161 | ||||||
chr14:104888208
|
A | G | 141 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(138): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.3739+230A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888208 | ||||||
chr14:104888733
|
A | C | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3739+755A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888733 | ||||||
chr14:104888735
|
G | A | 24 | a0002c0004t0002g0007a0002c0004t0002g0028a0002c0004t0002g0030others(21): Show | 33 | HG00408.hp2 HG00544.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.3739+757G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888735 | ||||||
chr14:104888848
|
G | T | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3740-772G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888848 | ||||||
chr14:104888964
|
C | T | 1 | a0001c0010t0002g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3740-656C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888964 | ||||||
chr14:104889015
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3740-605A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889015 | ||||||
chr14:104889042
|
C | T | 3 | a0001c0007t0008g0136a0001c0007t0008g0137a0001c0007t0008g0140 | 3 | HG02055.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3740-578C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889042 | ||||||
chr14:104889108
|
T | A | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3740-512T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889108 | ||||||
chr14:104889212
|
C | T | 119 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(116): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3740-408C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889212 | ||||||
chr14:104889294
|
C | T | 1 | a0012c0031t0001g0103 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3740-326C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889294 | ||||||
chr14:104889333
|
TG | T | 38 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(35): Show | 39 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.3740-285delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 104889333 | |||||
chr14:104889455
|
A | G | 1 | a0001c0005t0003g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3740-165A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889455 | ||||||
chr14:104889582
|
C | T | 1 | a0002c0009t0012g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3740-38C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889582 | ||||||
chr14:104889617
|
C | A | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | splice_region_variant&intron_variant | LOW | c.3740-3C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889617 | ||||||
chr14:104889800
|
G | C | 141 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(138): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.3878+42G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889800 | ||||||
chr14:104889834
|
C | T | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+76C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889834 | ||||||
chr14:104889872
|
C | T | 3 | a0001c0073t0002g0162a0001c0075t0002g0163a0026c0072t0002g0165 | 3 | HG02647.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3878+114C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889872 | ||||||
chr14:104889890
|
CTGGATGG others(25): Show |
C | 2 | a0008c0086t0002g0220a0021c0085t0002g0223 | 2 | NA18960.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.3878+145_3878+176d others(34): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889890 | |||||
chr14:104889903
|
CAAAT | C | 16 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(13): Show | 16 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878+146_3878+149d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889903 | ||||||
chr14:104889903
|
CAAATGGA others(1): Show |
C | 16 | a0001c0006t0005g0023a0001c0006t0007g0024a0001c0020t0002g0026others(13): Show | 17 | HG00438.hp1 HG01071.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3878+146_3878+153d others(10): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889903 | ||||||
chr14:104889903
|
CAAATGGA others(5): Show |
C | 79 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(76): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.3878+146_3878+157d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889903 | ||||||
chr14:104889904
|
A | G | 6 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(3): Show | 6 | HG01496.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3878+146A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889904 | ||||||
chr14:104889905
|
A | AATGG | 22 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0059others(19): Show | 25 | HG00741.hp2 HG01346.hp1 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.3878+191_3878+194d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | |||||
chr14:104889905
|
A | AATGGATG others(1): Show |
4 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0151others(1): Show | 4 | HG01496.hp2 NA18952.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.3878+187_3878+194d others(10): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | |||||
chr14:104889905
|
A | AATGGATG others(5): Show |
3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0085 | 3 | HG01167.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3878+183_3878+194d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | |||||
chr14:104889905
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3878+147A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889905 | ||||||
chr14:104889905
|
AATGG | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0035others(20): Show | 27 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.3878+191_3878+194d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | |||||
chr14:104889909
|
G | A | 16 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(13): Show | 16 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878+151G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889909 | ||||||
chr14:104889913
|
G | A | 16 | a0001c0006t0005g0023a0001c0006t0007g0024a0001c0020t0002g0026others(13): Show | 17 | HG00438.hp1 HG01071.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3878+155G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889913 | ||||||
chr14:104889915
|
T | G | 3 | a0001c0005t0003g0260a0001c0008t0003g0266a0001c0008t0003g0267 | 3 | HG02258.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3878+157T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889915 | ||||||
chr14:104889917
|
G | A | 79 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(76): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.3878+159G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889917 | ||||||
chr14:104889941
|
GATGGATG others(5): Show |
G | 4 | a0001c0005t0003g0032a0001c0005t0003g0256a0001c0008t0003g0265others(1): Show | 5 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3878+195_3878+206d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889941 | |||||
chr14:104889945
|
GATGGATG others(1): Show |
G | 11 | a0001c0005t0003g0014a0001c0005t0003g0260a0001c0008t0003g0014others(8): Show | 14 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3878+195_3878+202d others(10): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889945 | |||||
chr14:104889949
|
G | GATGGATG others(9): Show |
1 | a0001c0001t0001g0099 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.3878+194_3878+195i others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889949 | |||||
chr14:104889949
|
GATGA | G | 5 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0005t0003g0251others(2): Show | 5 | HG01255.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3878+195_3878+198d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889949 | |||||
chr14:104889951
|
TGAATGGA others(4): Show |
T | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+194_3878+204d others(13): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889951 | ||||||
chr14:104889953
|
A | G | 11 | a0001c0001t0001g0142a0001c0005t0003g0253a0001c0005t0003g0254others(8): Show | 12 | HG00733.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3878+195A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889953 | ||||||
chr14:104889957
|
G | A | 7 | a0001c0014t0001g0017a0001c0014t0001g0077a0004c0021t0006g0245others(4): Show | 8 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3878+199G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889957 | ||||||
chr14:104889963
|
T | A | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+205T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889963 | ||||||
chr14:104889966
|
A | C | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+208A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889966 | ||||||
chr14:104889968
|
A | G | 8 | a0001c0014t0001g0017a0001c0014t0001g0077a0004c0021t0006g0245others(5): Show | 9 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3878+210A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889968 | ||||||
chr14:104889969
|
G | GA | 7 | a0001c0014t0001g0017a0001c0014t0001g0077a0004c0021t0006g0245others(4): Show | 8 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3878+211_3878+212i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889969 | ||||||
chr14:104889970
|
G | T | 7 | a0001c0014t0001g0017a0001c0014t0001g0077a0004c0021t0006g0245others(4): Show | 8 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3878+212G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889970 | ||||||
chr14:104889971
|
A | AGGGT | 117 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(114): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.3878+224_3878+227d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889971 | |||||
chr14:104889971
|
A | T | 1 | a0018c0068t0019g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+213A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889971 | ||||||
chr14:104889986
|
A | G | 2 | a0001c0001t0001g0048a0001c0015t0001g0064 | 2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3878+228A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889986 | ||||||
chr14:104890044
|
A | G | 141 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(138): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.3878+286A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890044 | ||||||
chr14:104890103
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3878+345T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890103 | ||||||
chr14:104890136
|
G | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+378G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890136 | ||||||
chr14:104890161
|
CATGGATG others(5): Show |
C | 20 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(17): Show | 20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3878+420_3878+431d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890161 | |||||
chr14:104890186
|
A | G | 3 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3878+428A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890186 | ||||||
chr14:104890214
|
A | G | 19 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(16): Show | 19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3878+456A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890214 | ||||||
chr14:104890346
|
G | GTGGA | 22 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(19): Show | 26 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3878+603_3878+606d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890346 | |||||
chr14:104890354
|
A | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+596A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890354 | ||||||
chr14:104890358
|
A | ATGGAT | 119 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(116): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3878+601_3878+605d others(7): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890358 | |||||
chr14:104890373
|
G | C | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3878+615G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890373 | ||||||
chr14:104890390
|
G | GTGGA | 4 | a0001c0054t0001g0079a0008c0086t0002g0220a0021c0085t0002g0223others(1): Show | 4 | HG02809.hp2 HG02922.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3878+659_3878+662d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | |||||
chr14:104890390
|
G | GTGGATGG others(5): Show |
10 | a0001c0014t0001g0077a0001c0058t0001g0076a0001c0059t0001g0075others(7): Show | 10 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.3878+651_3878+662d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | |||||
chr14:104890390
|
G | GTGGATGG others(9): Show |
1 | a0001c0070t0001g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3878+647_3878+662d others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | |||||
chr14:104890390
|
G | GTGGATGG others(109): Show |
1 | a0001c0014t0001g0017 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3878+662_3878+663i others(118): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | |||||
chr14:104890390
|
GTGGA | G | 15 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0111others(12): Show | 18 | HG01074.hp2 HG01256.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.3878+659_3878+662d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | |||||
chr14:104890421
|
A | G | 2 | a0001c0054t0001g0079a0029c0052t0001g0047 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3878+663A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890421 | ||||||
chr14:104890531
|
T | C | 1 | a0001c0007t0001g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3878+773T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890531 | ||||||
chr14:104890566
|
G | GTGGA | 116 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(113): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.3878+828_3878+831d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890566 | |||||
chr14:104890566
|
G | GTGGATGG others(5): Show |
19 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(16): Show | 23 | HG01167.hp2 HG01255.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.3878+820_3878+831d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890566 | |||||
chr14:104890566
|
G | GTGGATGG others(9): Show |
1 | a0011c0027t0003g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3878+816_3878+831d others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890566 | |||||
chr14:104890590
|
G | A | 14 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(11): Show | 15 | HG00280.hp1 HG00438.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3878+832G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890590 | ||||||
chr14:104890593
|
A | G | 14 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(11): Show | 15 | HG00280.hp1 HG00438.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3878+835A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890593 | ||||||
chr14:104890662
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3878+904G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890662 | ||||||
chr14:104890698
|
G | GTGGATGG others(5): Show |
1 | a0001c0035t0013g0158 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3878+947_3878+958d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890698 | |||||
chr14:104890719
|
T | TG | 23 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(20): Show | 27 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.3878+963dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890719
|
T | TGGGTGGG others(34): Show |
1 | a0001c0010t0002g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3878+963_3878+964i others(43): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890719
|
T | TGGGTGGG others(33): Show |
1 | a0021c0085t0002g0223 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3878+963_3878+964i others(42): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890719
|
T | TGGGTGGG others(34): Show |
109 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(106): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3878+963_3878+964i others(43): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890719
|
T | TGGGTGGG others(74): Show |
4 | a0001c0062t0002g0177a0001c0065t0002g0268a0010c0025t0002g0269others(1): Show | 4 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3878+963_3878+964i others(83): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890719
|
T | TGGGTGGG others(78): Show |
1 | a0001c0061t0017g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3878+963_3878+964i others(87): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890719
|
T | TGGGTGGG others(34): Show |
2 | a0001c0017t0002g0173a0001c0017t0002g0174 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3878+963_3878+964i others(43): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | |||||
chr14:104890738
|
T | A | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+980T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890738 | ||||||
chr14:104890740
|
GATGA | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0142 | 3 | HG00639.hp1 HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3878+986_3878+989d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890740 | |||||
chr14:104890829
|
A | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1071A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890829 | ||||||
chr14:104890848
|
A | AATGAGTG others(25): Show |
1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3878+1107_3878+113 others(36): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890848 | |||||
chr14:104890897
|
A | G | 2 | a0001c0061t0017g0178a0001c0062t0002g0177 | 2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3878+1139A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890897 | ||||||
chr14:104890972
|
G | GGTGT | 4 | a0001c0007t0001g0114a0005c0016t0001g0021a0005c0016t0014g0088others(1): Show | 5 | HG02572.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3878+1218_3878+122 others(8): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890972 | |||||
chr14:104890989
|
G | A | 119 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(116): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3878+1231G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890989 | ||||||
chr14:104891014
|
A | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1256A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891014 | ||||||
chr14:104891048
|
T | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1290T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891048 | ||||||
chr14:104891050
|
A | T | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1292A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891050 | ||||||
chr14:104891052
|
T | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1294T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891052 | ||||||
chr14:104891053
|
G | T | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1295G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891053 | ||||||
chr14:104891058
|
G | C | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1300G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891058 | ||||||
chr14:104891068
|
TGGATGGA others(29): Show |
T | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1313_3878+134 others(40): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104891068 | |||||
chr14:104891110
|
G | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1352G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891110 | ||||||
chr14:104891124
|
T | G | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1366T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891124 | ||||||
chr14:104891126
|
C | T | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1368C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891126 | ||||||
chr14:104891139
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3878+1381C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891139 | ||||||
chr14:104891146
|
T | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1388T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891146 | ||||||
chr14:104891147
|
A | T | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1389A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891147 | ||||||
chr14:104891149
|
A | C | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1391A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891149 | ||||||
chr14:104891150
|
A | C | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1392A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891150 | ||||||
chr14:104891153
|
A | C | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1395A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891153 | ||||||
chr14:104891154
|
G | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1396G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891154 | ||||||
chr14:104891169
|
T | G | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1411T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891169 | ||||||
chr14:104891171
|
T | A | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1413T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891171 | ||||||
chr14:104891181
|
A | C | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1423A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891181 | ||||||
chr14:104891182
|
T | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1424T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891182 | ||||||
chr14:104891248
|
T | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1490T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891248 | ||||||
chr14:104891269
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3878+1511G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891269 | ||||||
chr14:104891299
|
T | A | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1541T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891299 | ||||||
chr14:104891325
|
G | C | 2 | a0001c0001t0001g0081a0001c0055t0001g0082 | 2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1567G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891325 | ||||||
chr14:104891326
|
G | T | 2 | a0001c0001t0001g0081a0001c0055t0001g0082 | 2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1568G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891326 | ||||||
chr14:104891328
|
G | A | 2 | a0001c0001t0001g0081a0001c0055t0001g0082 | 2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1570G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891328 | ||||||
chr14:104891329
|
C | A | 2 | a0001c0001t0001g0081a0001c0055t0001g0082 | 2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1571C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891329 | ||||||
chr14:104891332
|
G | T | 1 | a0001c0070t0001g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3878+1574G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891332 | ||||||
chr14:104891334
|
A | AG | 11 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0125others(8): Show | 12 | HG00544.hp1 HG00642.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.3878+1583dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104891334 | |||||
chr14:104891432
|
G | GGGAGGCC others(56): Show |
1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1543_3879-154 others(67): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104891432 | |||||
chr14:104891434
|
C | T | 18 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(15): Show | 19 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.3879-1542C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891434 | ||||||
chr14:104891435
|
G | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1541G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891435 | ||||||
chr14:104891437
|
C | G | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1539C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891437 | ||||||
chr14:104891439
|
C | A | 1 | a0002c0004t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1537C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891439 | ||||||
chr14:104891695
|
G | A | 81 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(78): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.3879-1281G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891695 | ||||||
chr14:104891777
|
A | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-1199A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891777 | ||||||
chr14:104891797
|
G | C | 1 | a0001c0010t0002g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3879-1179G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891797 | ||||||
chr14:104891798
|
C | G | 1 | a0001c0010t0002g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3879-1178C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891798 | ||||||
chr14:104891839
|
C | T | 1 | a0001c0003t0021g0199 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3879-1137C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891839 | ||||||
chr14:104891978
|
T | C | 119 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(116): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3879-998T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891978 | ||||||
chr14:104891983
|
G | A | 2 | a0022c0079t0001g0033a0028c0045t0001g0144 | 2 | HG00733.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3879-993G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891983 | ||||||
chr14:104891993
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3879-983C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891993 | ||||||
chr14:104891994
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3879-982T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891994 | ||||||
chr14:104892012
|
C | T | 119 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0027others(116): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.3879-964C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892012 | ||||||
chr14:104892175
|
G | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-801G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892175 | ||||||
chr14:104892188
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3879-788T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892188 | ||||||
chr14:104892224
|
A | G | 1 | a0001c0019t0002g0168 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3879-752A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892224 | ||||||
chr14:104892227
|
TGACGAGG others(6): Show |
T | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3879-747_3879-735d others(15): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104892227 | |||||
chr14:104892230
|
C | T | 1 | a0001c0005t0003g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3879-746C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892230 | ||||||
chr14:104892251
|
A | T | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-725A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892251 | ||||||
chr14:104892275
|
C | T | 21 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(18): Show | 25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.3879-701C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892275 | ||||||
chr14:104892292
|
C | T | 20 | a0001c0017t0002g0170a0001c0017t0002g0173a0001c0017t0002g0174others(17): Show | 20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3879-684C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892292 | ||||||
chr14:104892306
|
T | A | 1 | a0009c0024t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-670T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892306 | ||||||
chr14:104892322
|
T | C | 22 | a0001c0005t0003g0014a0001c0005t0003g0032a0001c0005t0003g0251others(19): Show | 26 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3879-654T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892322 | ||||||
chr14:104892391
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3879-585T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892391 | ||||||
chr14:104892441
|
ATCTGCCC others(10): Show |
A | 21 | a0001c0006t0005g0036a0001c0006t0005g0074a0001c0006t0005g0154others(18): Show | 22 | HG00733.hp1 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.3879-504_3879-488d others(19): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104892441 | |||||
chr14:104892547
|
C | T | 1 | a0001c0002t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3879-429C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892547 | ||||||
chr14:104892662
|
C | G | 3 | a0001c0065t0002g0268a0010c0025t0002g0269a0010c0025t0002g0270 | 3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3879-314C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892662 | ||||||
chr14:104892670
|
G | T | 1 | a0001c0003t0002g0222 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3879-306G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892670 | ||||||
chr14:104892706
|
T | C | 1 | a0019c0044t0001g0129 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3879-270T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892706 | ||||||
chr14:104892740
|
C | T | 1 | a0001c0002t0002g0224 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3879-236C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892740 | ||||||
chr14:104892956
|
G | A | 9 | a0001c0014t0001g0017a0001c0014t0001g0077a0001c0070t0001g0166others(6): Show | 10 | HG00733.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3879-20G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892956 | ||||||
chr14:104892968
|
G | A | 13 | a0001c0006t0005g0023a0001c0006t0005g0036a0001c0006t0005g0074others(10): Show | 14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.3879-8G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892968 | ||||||
chr14:104892969
|
G | C | 120 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(117): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
splice_region_variant&intron_variant | LOW | c.3879-7G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892969 | ||||||
chr14:104892970
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA18982.hp1 | splice_region_variant&intron_variant | LOW | c.3879-6C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892970 | ||||||
chr14:104893179
|
C | T | 2 | a0010c0025t0002g0269a0010c0025t0002g0270 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4038+44C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893179 | ||||||
chr14:104893180
|
G | A | 1 | a0001c0053t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4038+45G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893180 | ||||||
chr14:104893211
|
T | C | 1 | a0001c0015t0001g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4038+76T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893211 | ||||||
chr14:104893219
|
C | T | 1 | a0001c0037t0005g0157 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4038+84C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893219 | ||||||
chr14:104893297
|
C | T | 1 | a0001c0011t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4038+162C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893297 | ||||||
chr14:104893306
|
C | G | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4038+171C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893306 | ||||||
chr14:104893322
|
C | T | 120 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(117): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.4038+187C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893322 | ||||||
chr14:104893413
|
C | T | 1 | a0001c0002t0002g0027 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4039-110C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893413 | ||||||
chr14:104893490
|
T | C | 155 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(152): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.4039-33T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893490 | ||||||
chr14:104893941
|
G | A | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4271+92G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893941 | ||||||
chr14:104893954
|
C | G | 1 | a0001c0019t0002g0168 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4271+105C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893954 | ||||||
chr14:104893956
|
C | T | 5 | a0001c0061t0017g0178a0001c0062t0002g0177a0001c0065t0002g0268others(2): Show | 5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4271+107C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893956 | ||||||
chr14:104893964
|
C | T | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4271+115C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893964 | ||||||
chr14:104893991
|
G | A | 1 | a0001c0008t0003g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4271+142G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893991 | ||||||
chr14:104894018
|
C | T | 81 | a0001c0001t0002g0243a0001c0002t0002g0002a0001c0002t0002g0005others(78): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.4271+169C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894018 | ||||||
chr14:104894026
|
A | T | 1 | a0002c0064t0002g0171 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4271+177A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894026 | ||||||
chr14:104894164
|
C | T | 1 | a0001c0010t0002g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4272-121C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894164 | ||||||
chr14:104894228
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4272-57C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894228 | ||||||
chr14:104894385
|
G | A | 1 | a0030c0040t0011g0273 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.4365+7G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 17/18 | chr14 | 104894385 | ||||||
chr14:104894409
|
T | C | 155 | a0001c0001t0001g0056a0001c0001t0002g0243a0001c0002t0002g0002others(152): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.4365+31T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 17/18 | chr14 | 104894409 | ||||||
chr14:104894610
|
G | A | 1 | a0001c0003t0020g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4417+22G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 18/18 | chr14 | 104894610 |