geneid | 79959 |
---|---|
ensemblid | ENSG00000101624.11 |
hgncid | 25727 |
symbol | CEP76 |
name | centrosomal protein 76 |
refseq_nuc | NM_024899.4 |
refseq_prot | NP_079175.2 |
ensembl_nuc | ENST00000262127.7 |
ensembl_prot | ENSP00000262127.2 |
mane_status | MANE Select |
chr | chr18 |
start | 12672625 |
end | 12702723 |
strand | - |
ver | v1.2 |
region | chr18:12672625-12702723 |
region5000 | chr18:12667625-12707723 |
regionname0 | CEP76_chr18_12672625_12702723 |
regionname5000 | CEP76_chr18_12667625_12707723 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 659 | 365 | 88 | 67 | 154 | 12 | 42 | 121 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0002 | 0/0 | 659 | 11 | 0 | 3 | 8 | 0 | 0 | 7 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0003 | 0/0 | 659 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0004 | 0/0 | 659 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0005 | 0/0 | 659 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0006 | 0/0 | 659 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1980 | 365 | 88 | 67 | 154 | 12 | 42 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
c0002 | 0/0 | 1980 | 11 | 0 | 3 | 8 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
c0003 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
c0004 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
c0005 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
c0006 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 916 | 189 | 42 | 31 | 77 | 8 | 30 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0002 | 0/0 | 916 | 97 | 23 | 22 | 45 | 1 | 6 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0003 | 0/0 | 916 | 59 | 3 | 10 | 42 | 1 | 3 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0004 | 0/1 | 916 | 19 | 12 | 3 | 0 | 1 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0005 | 0/0 | 916 | 6 | 3 | 2 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0006 | 0/0 | 916 | 6 | 6 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0007 | 0/0 | 916 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0008 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0009 | 0/0 | 916 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
t0010 | 0/0 | 916 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0002 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0005 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0015 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0034 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1980 | 365 | 88 | 67 | 154 | 12 | 42 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0002c0002 | 0/0 | 1980 | 11 | 0 | 3 | 8 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0003c0003 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0004c0005 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0005c0004 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0006c0006 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2895 | 174 | 40 | 28 | 67 | 8 | 30 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0002 | 0/0 | 2895 | 97 | 23 | 22 | 45 | 1 | 6 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0003 | 0/0 | 2895 | 59 | 3 | 10 | 42 | 1 | 3 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0004 | 0/1 | 2895 | 19 | 12 | 3 | 0 | 1 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0005 | 0/0 | 2895 | 6 | 3 | 2 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0006 | 0/0 | 2895 | 6 | 6 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0007 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0008 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0009 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0001c0001t0010 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0002c0002t0001 | 0/0 | 2895 | 11 | 0 | 3 | 8 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0003c0003t0001 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0004c0005t0001 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0005c0004t0001 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
a0006c0006t0001 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | copy fasta | chr18 | 12667625 | 12707723 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0034 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0002 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0005 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0004c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0005c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
a0006c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0114 | EUR | FIN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0197 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0113 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02965 | hp1 | a0006 | c0006 | t0001 | g0057 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0196 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03486 | hp1 | a0005 | c0004 | t0001 | g0191 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0280 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0267 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19011 | hp2 | a0004 | c0005 | t0001 | g0138 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ASW | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0259 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0187 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0111 | REF | REF | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0034 | REF | REF | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:12674674
|
C | T | 1 | a0004 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1703G>A | p.Arg568His | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/12 | 1878/2895 | 1703/1980 | 568/659 | chr18 | 12674674 | ||
chr18:12686401
|
C | T | 1 | a0003 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.983G>A | p.Arg328Gln | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/12 | 1158/2895 | 983/1980 | 328/659 | chr18 | 12686401 | ||
chr18:12697231
|
A | G | 1 | a0005 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.698T>C | p.Met233Thr | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/12 | 873/2895 | 698/1980 | 233/659 | chr18 | 12697231 | ||
chr18:12697355
|
T | C | 1 | a0006 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.574A>G | p.Ile192Val | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/12 | 749/2895 | 574/1980 | 192/659 | chr18 | 12697355 | ||
chr18:12698984
|
C | T | 2 | a0002a0003 | 12 | HG01192.hp1 HG01257.hp1 HG02004.hp1 others(9): Show |
missense_variant | MODERATE | c.515G>A | p.Ser172Asn | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/12 | 690/2895 | 515/1980 | 172/659 | chr18 | 12698984 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:12672656
|
A | G | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0007 | 26 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 709 | chr18 | 12672656 | |||||
chr18:12672934
|
G | A | 1 | a0001c0001t0010 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 431 | chr18 | 12672934 | |||||
chr18:12672957
|
A | G | 1 | a0001c0001t0007 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*408T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 408 | chr18 | 12672957 | |||||
chr18:12673137
|
C | G | 1 | a0001c0001t0006 | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 228 | chr18 | 12673137 | |||||
chr18:12673188
|
T | C | 2 | a0001c0001t0006a0001c0001t0008 | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 177 | chr18 | 12673188 | |||||
chr18:12673196
|
G | A | 1 | a0001c0001t0005 | 6 | HG01243.hp2 HG01256.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*169C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 169 | chr18 | 12673196 | |||||
chr18:12673232
|
T | G | 1 | a0001c0001t0006 | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*133A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 133 | chr18 | 12673232 | |||||
chr18:12702594
|
C | T | 1 | a0001c0001t0009 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/12 | 46 | chr18 | 12702594 | |||||
chr18:12702611
|
G | A | 2 | a0001c0001t0002a0001c0001t0009 | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/12 | chr18 | 12702611 | ||||||
chr18:12702706
|
G | C | 2 | a0001c0001t0003a0001c0001t0010 | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-158C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/12 | 158 | chr18 | 12702706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:12673532
|
TAAG | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0236 | 4 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842-32_1842-30del others(3): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673532 | ||||||
chr18:12673540
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842-37C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673540 | ||||||
chr18:12673575
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1842-72G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673575 | ||||||
chr18:12673708
|
C | T | 3 | a0001c0001t0004g0009a0001c0001t0004g0180a0001c0001t0004g0181 | 6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1842-205G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673708 | ||||||
chr18:12673722
|
A | G | 52 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(49): Show | 71 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1842-219T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673722 | ||||||
chr18:12673807
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1842-304C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673807 | ||||||
chr18:12673849
|
A | C | 191 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0017others(188): Show | 252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1842-346T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673849 | ||||||
chr18:12673868
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1842-365C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673868 | ||||||
chr18:12674422
|
G | T | 1 | a0006c0006t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1841+114C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12674422 | ||||||
chr18:12674441
|
T | TA | 6 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0156others(3): Show | 6 | HG01928.hp2 HG03710.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1841+94dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12674441 | ||||||
chr18:12674441
|
TA | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(27): Show | 34 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1841+94delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12674441 | ||||||
chr18:12674778
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1624-25T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12674778 | ||||||
chr18:12674852
|
G | T | 10 | a0001c0001t0002g0212a0001c0001t0002g0220a0001c0001t0002g0221others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1624-99C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12674852 | ||||||
chr18:12674965
|
C | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0236 | 4 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-212G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12674965 | ||||||
chr18:12675077
|
T | TACATTTT others(3): Show |
6 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-325_1624-324i others(12): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675077 | ||||||
chr18:12675077
|
T | TATATTTT others(3): Show |
66 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(63): Show | 89 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1624-334_1624-325d others(12): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675077 | ||||||
chr18:12675159
|
G | C | 2 | a0001c0001t0006g0047a0001c0001t0006g0062 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1624-406C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675159 | ||||||
chr18:12675318
|
T | C | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1624-565A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675318 | ||||||
chr18:12675345
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1624-592C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675345 | ||||||
chr18:12675568
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0140 | 2 | HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1624-815A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675568 | ||||||
chr18:12675680
|
AT | A | 6 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-928delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675680 | ||||||
chr18:12675700
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1624-947T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675700 | ||||||
chr18:12675904
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1624-1151T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675904 | ||||||
chr18:12675924
|
C | T | 45 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1624-1171G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675924 | ||||||
chr18:12675937
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1624-1184C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675937 | ||||||
chr18:12675958
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1624-1205G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675958 | ||||||
chr18:12676010
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1624-1257C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676010 | ||||||
chr18:12676174
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1624-1421G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676174 | ||||||
chr18:12676175
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(3): Show | 7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-1422C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676175 | ||||||
chr18:12676279
|
C | CT | 78 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0053others(75): Show | 103 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1624-1527dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676279 | ||||||
chr18:12676279
|
C | CTT | 5 | a0001c0001t0002g0217a0001c0001t0002g0229a0001c0001t0003g0043others(2): Show | 6 | HG03688.hp1 NA18944.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-1528_1624-152 others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676279 | ||||||
chr18:12676350
|
C | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1624-1597G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676350 | ||||||
chr18:12676459
|
G | GAGAT | 71 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0010others(68): Show | 96 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1623+1646_1623+164 others(8): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676459 | ||||||
chr18:12676476
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1623+1633G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676476 | ||||||
chr18:12676765
|
G | A | 189 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0017others(186): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1623+1344C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676765 | ||||||
chr18:12676773
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1623+1336T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676773 | ||||||
chr18:12676786
|
A | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0127others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+1323T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676786 | ||||||
chr18:12677033
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1623+1076T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677033 | ||||||
chr18:12677045
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1623+1064G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677045 | ||||||
chr18:12677184
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1623+925C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677184 | ||||||
chr18:12677237
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0136a0001c0001t0001g0151 | 4 | HG01081.hp2 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+872G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677237 | ||||||
chr18:12677299
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1623+810C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677299 | ||||||
chr18:12677394
|
C | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG01952.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1623+715G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677394 | ||||||
chr18:12677422
|
G | A | 3 | a0001c0001t0002g0040a0001c0001t0002g0213a0001c0001t0002g0231 | 4 | HG00558.hp1 HG00597.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+687C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677422 | ||||||
chr18:12677458
|
C | CA | 27 | a0001c0001t0001g0046a0001c0001t0001g0072a0001c0001t0001g0073others(24): Show | 29 | HG00621.hp1 HG00621.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1623+650dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677458 | ||||||
chr18:12677458
|
CA | C | 38 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(35): Show | 46 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1623+650delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677458 | ||||||
chr18:12677458
|
CAA | C | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(49): Show | 71 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1623+649_1623+650d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677458 | ||||||
chr18:12677696
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1623+413G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677696 | ||||||
chr18:12677740
|
T | C | 1 | a0001c0001t0003g0281 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1623+369A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677740 | ||||||
chr18:12677935
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1623+174C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677935 | ||||||
chr18:12678031
|
C | T | 2 | a0001c0001t0001g0048a0006c0006t0001g0057 | 2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1623+78G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12678031 | ||||||
chr18:12678487
|
A | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1290-45T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678487 | ||||||
chr18:12678697
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290-255C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678697 | ||||||
chr18:12678699
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1290-257A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678699 | ||||||
chr18:12678722
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1290-280C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678722 | ||||||
chr18:12678726
|
CA | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0192a0005c0004t0001g0191 | 5 | HG01884.hp2 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1290-285delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678726 | ||||||
chr18:12678729
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1290-287C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678729 | ||||||
chr18:12678784
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290-342G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678784 | ||||||
chr18:12678842
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290-400C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678842 | ||||||
chr18:12678926
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1290-484G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678926 | ||||||
chr18:12678950
|
A | G | 22 | a0001c0001t0004g0009a0001c0001t0004g0033a0001c0001t0004g0056others(19): Show | 26 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1290-508T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678950 | ||||||
chr18:12679093
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1290-651C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679093 | ||||||
chr18:12679326
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1290-884T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679326 | ||||||
chr18:12679388
|
G | GAGGCAGG others(12): Show |
1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1290-965_1290-947d others(21): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679388 | ||||||
chr18:12679401
|
C | T | 1 | a0006c0006t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1290-959G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679401 | ||||||
chr18:12679413
|
G | GGAAGCAC others(12): Show |
1 | a0001c0001t0005g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1290-990_1290-972d others(21): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679413 | ||||||
chr18:12679413
|
GGAAGCAC others(12): Show |
G | 1 | a0001c0001t0002g0234 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1290-990_1290-972d others(21): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679413 | ||||||
chr18:12679760
|
C | G | 2 | a0001c0001t0006g0047a0001c0001t0006g0062 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1289+902G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679760 | ||||||
chr18:12679829
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1289+833C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679829 | ||||||
chr18:12679864
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1289+798T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679864 | ||||||
chr18:12680052
|
C | CA | 9 | a0001c0001t0002g0035a0001c0001t0003g0281a0001c0001t0004g0110others(6): Show | 10 | HG00280.hp2 HG01192.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1289+609dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680052 | ||||||
chr18:12680084
|
AT | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 6 | NA18946.hp2 NA18950.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1289+577delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680084 | ||||||
chr18:12680274
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1289+388A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680274 | ||||||
chr18:12680519
|
C | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1289+143G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680519 | ||||||
chr18:12680522
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1289+140C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680522 | ||||||
chr18:12680562
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1289+100T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680562 | ||||||
chr18:12680596
|
C | CA | 5 | a0001c0001t0002g0035a0001c0001t0002g0211a0001c0001t0002g0223others(2): Show | 6 | HG00738.hp1 HG01361.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1289+65dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680596 | ||||||
chr18:12680596
|
CA | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(161): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1289+65delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680596 | ||||||
chr18:12680596
|
CAA | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(23): Show | 29 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1289+64_1289+65del others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680596 | ||||||
chr18:12680969
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1123-141G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12680969 | ||||||
chr18:12681130
|
G | A | 1 | a0001c0001t0006g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1123-302C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681130 | ||||||
chr18:12681198
|
C | CA | 31 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(28): Show | 34 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1123-371dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681198 | ||||||
chr18:12681255
|
CA | C | 1 | a0001c0001t0002g0013 | 3 | HG01884.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1123-428delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681255 | ||||||
chr18:12681256
|
A | AT | 35 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(32): Show | 40 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1123-429dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | ||||||
chr18:12681256
|
A | ATT | 22 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0068others(19): Show | 26 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1123-430_1123-429d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | ||||||
chr18:12681256
|
A | T | 7 | a0001c0001t0001g0171a0001c0001t0002g0037a0001c0001t0002g0216others(4): Show | 8 | HG00673.hp1 HG02027.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1123-428T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | ||||||
chr18:12681256
|
AT | A | 21 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(18): Show | 23 | HG00408.hp1 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.1123-429delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | ||||||
chr18:12681256
|
ATT | A | 38 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(35): Show | 56 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1123-430_1123-429d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | ||||||
chr18:12681437
|
CAG | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1123-611_1123-610d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681437 | ||||||
chr18:12681691
|
A | G | 22 | a0001c0001t0004g0009a0001c0001t0004g0033a0001c0001t0004g0056others(19): Show | 26 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1123-863T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681691 | ||||||
chr18:12681711
|
GAAC | G | 5 | a0001c0001t0006g0047a0001c0001t0006g0059a0001c0001t0006g0060others(2): Show | 5 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1123-886_1123-884d others(5): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681711 | ||||||
chr18:12681947
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 7 | HG02257.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-1119C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681947 | ||||||
chr18:12681996
|
T | TA | 7 | a0001c0001t0001g0147a0001c0001t0006g0047a0001c0001t0006g0058others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-1169dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681996 | ||||||
chr18:12682135
|
G | T | 7 | a0001c0001t0002g0036a0001c0001t0002g0203a0001c0001t0002g0204others(4): Show | 8 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123-1307C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682135 | ||||||
chr18:12682171
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1123-1343A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682171 | ||||||
chr18:12682214
|
G | A | 22 | a0001c0001t0004g0009a0001c0001t0004g0033a0001c0001t0004g0056others(19): Show | 26 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1123-1386C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682214 | ||||||
chr18:12682698
|
G | A | 1 | a0001c0001t0003g0275 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1123-1870C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682698 | ||||||
chr18:12682936
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1123-2108C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682936 | ||||||
chr18:12682970
|
A | T | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1123-2142T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682970 | ||||||
chr18:12683116
|
C | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-2288G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683116 | ||||||
chr18:12683119
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1123-2291C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683119 | ||||||
chr18:12683186
|
C | CA | 28 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0046others(25): Show | 33 | HG00642.hp2 HG00741.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1123-2359dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAA | 7 | a0001c0001t0002g0214a0001c0001t0006g0047a0001c0001t0006g0058others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-2360_1123-235 others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAA | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(5): Show | 11 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1123-2364_1123-235 others(10): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1123-2370_1123-235 others(16): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(6): Show |
23 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0003g0003others(20): Show | 33 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1123-2371_1123-235 others(17): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(7): Show |
23 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0052others(20): Show | 33 | HG00544.hp1 HG00673.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1123-2372_1123-235 others(18): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0051a0001c0001t0003g0280 | 2 | HG03579.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1123-2373_1123-235 others(19): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1123-2374_1123-235 others(20): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1123-2376_1123-235 others(22): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(13): Show |
1 | a0006c0006t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1123-2359_1123-235 others(24): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683186
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1123-2359_1123-235 others(27): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | ||||||
chr18:12683345
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1123-2517G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683345 | ||||||
chr18:12683469
|
A | G | 7 | a0001c0001t0002g0036a0001c0001t0002g0203a0001c0001t0002g0204others(4): Show | 8 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123-2641T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683469 | ||||||
chr18:12683550
|
A | C | 1 | a0001c0001t0005g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1122+2712T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683550 | ||||||
chr18:12683567
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1122+2695T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683567 | ||||||
chr18:12683640
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1122+2622T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683640 | ||||||
chr18:12683806
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1122+2456T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683806 | ||||||
chr18:12683991
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1122+2271T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683991 | ||||||
chr18:12683999
|
T | C | 1 | a0001c0001t0002g0035 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1122+2263A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683999 | ||||||
chr18:12684033
|
A | C | 1 | a0001c0001t0002g0215 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1122+2229T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684033 | ||||||
chr18:12684045
|
G | T | 1 | a0001c0001t0002g0215 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1122+2217C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684045 | ||||||
chr18:12684049
|
G | T | 1 | a0001c0001t0002g0215 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1122+2213C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684049 | ||||||
chr18:12684063
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1122+2199G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684063 | ||||||
chr18:12684064
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1122+2198C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684064 | ||||||
chr18:12684088
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+2174C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684088 | ||||||
chr18:12684088
|
G | T | 1 | a0001c0001t0007g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1122+2174C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684088 | ||||||
chr18:12684097
|
T | C | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+2165A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684097 | ||||||
chr18:12684171
|
G | A | 1 | a0001c0001t0005g0187 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1122+2091C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684171 | ||||||
chr18:12684180
|
A | T | 1 | a0001c0001t0003g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1122+2082T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684180 | ||||||
chr18:12684202
|
C | T | 1 | a0001c0001t0002g0035 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1122+2060G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684202 | ||||||
chr18:12684282
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1122+1980A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684282 | ||||||
chr18:12684335
|
G | C | 6 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122+1927C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684335 | ||||||
chr18:12684421
|
C | T | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122+1841G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684421 | ||||||
chr18:12684460
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1122+1802A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684460 | ||||||
chr18:12684485
|
GT | G | 71 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 94 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1122+1776delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684485 | ||||||
chr18:12684492
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1122+1770A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684492 | ||||||
chr18:12684536
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1122+1726C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684536 | ||||||
chr18:12684697
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1122+1565C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684697 | ||||||
chr18:12684700
|
C | G | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122+1562G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684700 | ||||||
chr18:12684925
|
C | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(16): Show | 26 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1122+1337G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684925 | ||||||
chr18:12685005
|
A | T | 1 | a0001c0001t0009g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1122+1257T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685005 | ||||||
chr18:12685113
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1122+1149C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685113 | ||||||
chr18:12685202
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0123 | 3 | HG02698.hp2 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122+1060C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685202 | ||||||
chr18:12685322
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1122+940C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685322 | ||||||
chr18:12685346
|
C | G | 64 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0010others(61): Show | 88 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1122+916G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685346 | ||||||
chr18:12685396
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1122+866G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685396 | ||||||
chr18:12685405
|
A | G | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+857T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685405 | ||||||
chr18:12685575
|
G | A | 45 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1122+687C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685575 | ||||||
chr18:12685607
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1122+655G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685607 | ||||||
chr18:12685637
|
AT | A | 67 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 90 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1122+624delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685637 | ||||||
chr18:12685638
|
T | G | 1 | a0001c0001t0002g0213 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1122+624A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685638 | ||||||
chr18:12685639
|
T | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1122+623A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685639 | ||||||
chr18:12685658
|
T | A | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1122+604A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685658 | ||||||
chr18:12685695
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122+567C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685695 | ||||||
chr18:12685717
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1122+545G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685717 | ||||||
chr18:12685751
|
C | T | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1122+511G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685751 | ||||||
chr18:12685900
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1122+362C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685900 | ||||||
chr18:12685904
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1122+358A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685904 | ||||||
chr18:12685974
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1122+288T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685974 | ||||||
chr18:12685984
|
A | T | 45 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1122+278T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685984 | ||||||
chr18:12686029
|
A | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(3): Show | 7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+233T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686029 | ||||||
chr18:12686050
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122+212T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686050 | ||||||
chr18:12686063
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1122+199A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686063 | ||||||
chr18:12686091
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1122+171G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686091 | ||||||
chr18:12686247
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 7 | HG02257.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+15T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686247 | ||||||
chr18:12686464
|
G | C | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-14C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12686464 | ||||||
chr18:12686674
|
G | A | 45 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.934-224C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12686674 | ||||||
chr18:12686764
|
G | C | 39 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(36): Show | 58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.934-314C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12686764 | ||||||
chr18:12687028
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.934-578C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687028 | ||||||
chr18:12687139
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-689G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687139 | ||||||
chr18:12687254
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-804A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687254 | ||||||
chr18:12687414
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.934-964A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687414 | ||||||
chr18:12687454
|
A | AT | 13 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0001g0103others(10): Show | 13 | HG00438.hp2 HG01109.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-1005dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687454 | ||||||
chr18:12687454
|
AT | A | 18 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0049others(15): Show | 20 | HG00140.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.934-1005delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687454 | ||||||
chr18:12687474
|
G | T | 1 | a0001c0001t0003g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.934-1024C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687474 | ||||||
chr18:12687669
|
T | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0244 | 2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.934-1219A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687669 | ||||||
chr18:12687693
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.934-1243A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687693 | ||||||
chr18:12687713
|
A | G | 6 | a0001c0001t0001g0106a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | NA18948.hp2 NA18955.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-1263T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687713 | ||||||
chr18:12687773
|
AAC | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.934-1325_934-1324d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687773 | ||||||
chr18:12687906
|
G | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(3): Show | 7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-1456C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687906 | ||||||
chr18:12687926
|
T | G | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.934-1476A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687926 | ||||||
chr18:12687970
|
A | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0153a0001c0001t0004g0110others(2): Show | 5 | HG02738.hp2 HG03239.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-1520T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687970 | ||||||
chr18:12688087
|
C | CA | 3 | a0001c0001t0004g0009a0001c0001t0004g0180a0001c0001t0004g0181 | 6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-1638dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688087 | ||||||
chr18:12688146
|
G | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.934-1696C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688146 | ||||||
chr18:12688156
|
G | C | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-1706C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688156 | ||||||
chr18:12688228
|
C | CA | 8 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0003g0281others(5): Show | 8 | HG01169.hp2 HG01361.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-1779dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688228 | ||||||
chr18:12688228
|
CA | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.934-1779delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688228 | ||||||
chr18:12688243
|
A | C | 2 | a0001c0001t0001g0063a0001c0001t0004g0181 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.934-1793T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688243 | ||||||
chr18:12688279
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(13): Show | 23 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.934-1829C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688279 | ||||||
chr18:12688390
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.934-1940A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688390 | ||||||
chr18:12688423
|
C | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(3): Show | 7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-1973G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688423 | ||||||
chr18:12688609
|
C | A | 2 | a0001c0001t0006g0047a0001c0001t0006g0062 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.934-2159G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688609 | ||||||
chr18:12688633
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.934-2183C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688633 | ||||||
chr18:12688684
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.934-2234G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688684 | ||||||
chr18:12688701
|
A | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(16): Show | 26 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.934-2251T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688701 | ||||||
chr18:12688729
|
T | A | 1 | a0001c0001t0005g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.934-2279A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688729 | ||||||
chr18:12688880
|
C | T | 1 | a0006c0006t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.934-2430G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688880 | ||||||
chr18:12688892
|
G | T | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0010others(58): Show | 83 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.934-2442C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688892 | ||||||
chr18:12688911
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.933+2448C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688911 | ||||||
chr18:12689014
|
T | C | 61 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(58): Show | 81 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.933+2345A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689014 | ||||||
chr18:12689280
|
A | AAGC | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+2076_933+2078d others(5): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689280 | ||||||
chr18:12689587
|
T | TTCAG | 43 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0003g0003others(40): Show | 62 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.933+1771_933+1772i others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689587 | ||||||
chr18:12689638
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 12 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+1721A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689638 | ||||||
chr18:12689764
|
T | TTA | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(10): Show | 16 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+1593_933+1594d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689764 | ||||||
chr18:12689782
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.933+1577T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689782 | ||||||
chr18:12689786
|
T | C | 7 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+1573A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689786 | ||||||
chr18:12689859
|
C | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(16): Show | 26 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.933+1500G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689859 | ||||||
chr18:12689866
|
T | A | 1 | a0001c0001t0003g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.933+1493A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689866 | ||||||
chr18:12689911
|
C | T | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+1448G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689911 | ||||||
chr18:12689923
|
G | T | 1 | a0001c0001t0001g0017 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.933+1436C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689923 | ||||||
chr18:12689986
|
G | A | 5 | a0001c0001t0006g0047a0001c0001t0006g0059a0001c0001t0006g0060others(2): Show | 5 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+1373C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689986 | ||||||
chr18:12690030
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.933+1329G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690030 | ||||||
chr18:12690078
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.933+1281G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690078 | ||||||
chr18:12690080
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.933+1279G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690080 | ||||||
chr18:12690085
|
GGC | G | 45 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.933+1272_933+1273d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690085 | ||||||
chr18:12690102
|
C | T | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+1257G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690102 | ||||||
chr18:12690163
|
T | C | 1 | a0001c0001t0003g0044 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.933+1196A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690163 | ||||||
chr18:12690375
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.933+984T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690375 | ||||||
chr18:12690462
|
G | GT | 10 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0002g0036others(7): Show | 11 | HG01167.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.933+896dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690462 | ||||||
chr18:12690462
|
G | GTT | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.933+895_933+896dup others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690462 | ||||||
chr18:12690478
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.933+881G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690478 | ||||||
chr18:12690503
|
C | T | 1 | a0001c0001t0003g0261 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.933+856G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690503 | ||||||
chr18:12690504
|
G | A | 1 | a0001c0001t0003g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.933+855C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690504 | ||||||
chr18:12690532
|
T | C | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+827A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690532 | ||||||
chr18:12690548
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.933+811G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690548 | ||||||
chr18:12690581
|
G | A | 2 | a0001c0001t0001g0048a0006c0006t0001g0057 | 2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.933+778C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690581 | ||||||
chr18:12690606
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.933+753G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690606 | ||||||
chr18:12690706
|
C | T | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.933+653G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690706 | ||||||
chr18:12690840
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.933+519A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690840 | ||||||
chr18:12690939
|
G | GC | 50 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0050others(47): Show | 71 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.933+419dupG | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690939 | ||||||
chr18:12690941
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.933+418G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690941 | ||||||
chr18:12691043
|
G | GTTAAACA others(27): Show |
1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.933+282_933+315dup others(34): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12691043 | ||||||
chr18:12691546
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.805-59A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691546 | ||||||
chr18:12691558
|
T | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.805-71A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691558 | ||||||
chr18:12691611
|
A | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.805-124T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691611 | ||||||
chr18:12691630
|
C | G | 1 | a0006c0006t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805-143G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691630 | ||||||
chr18:12691646
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.805-159G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691646 | ||||||
chr18:12691684
|
T | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.805-197A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691684 | ||||||
chr18:12691709
|
A | AT | 67 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0022others(64): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.805-223dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691709 | ||||||
chr18:12691817
|
G | A | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.805-330C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691817 | ||||||
chr18:12691875
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.805-388A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691875 | ||||||
chr18:12691952
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.805-465G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691952 | ||||||
chr18:12691961
|
C | T | 7 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.805-474G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691961 | ||||||
chr18:12692038
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.805-551C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692038 | ||||||
chr18:12692241
|
G | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(9): Show | 15 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-754C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692241 | ||||||
chr18:12692265
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.805-778C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692265 | ||||||
chr18:12692273
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.805-786C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692273 | ||||||
chr18:12692315
|
C | CA | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 28 | HG00597.hp2 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.805-829dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692315 | ||||||
chr18:12692373
|
T | C | 1 | a0001c0001t0004g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805-886A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692373 | ||||||
chr18:12692447
|
G | A | 7 | a0001c0001t0002g0036a0001c0001t0002g0203a0001c0001t0002g0204others(4): Show | 8 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-960C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692447 | ||||||
chr18:12692477
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.805-990T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692477 | ||||||
chr18:12692561
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.805-1074G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692561 | ||||||
chr18:12692717
|
G | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.805-1230C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692717 | ||||||
chr18:12693066
|
C | T | 2 | a0001c0001t0005g0178a0001c0001t0005g0179 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.805-1579G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693066 | ||||||
chr18:12693334
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.805-1847C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693334 | ||||||
chr18:12693656
|
A | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+1598T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693656 | ||||||
chr18:12693676
|
A | G | 72 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0010others(69): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.804+1578T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693676 | ||||||
chr18:12693684
|
G | A | 6 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1570C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693684 | ||||||
chr18:12693707
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(17): Show | 27 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+1547G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693707 | ||||||
chr18:12693736
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1518A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693736 | ||||||
chr18:12693742
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1512G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693742 | ||||||
chr18:12693746
|
GCACTCCA others(39): Show |
G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1462_804+1507d others(48): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693746 | ||||||
chr18:12693768
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.804+1486G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693768 | ||||||
chr18:12693805
|
T | A | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.804+1449A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693805 | ||||||
chr18:12693852
|
A | ATGTATAT others(6): Show |
1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1401_804+1402i others(15): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693852 | ||||||
chr18:12693853
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1401C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693853 | ||||||
chr18:12694058
|
GCTGGACT others(18): Show |
G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1171_804+1195d others(27): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694058 | ||||||
chr18:12694085
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1169A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694085 | ||||||
chr18:12694089
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1165G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694089 | ||||||
chr18:12694090
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1164G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694090 | ||||||
chr18:12694122
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1132T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694122 | ||||||
chr18:12694133
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1121A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694133 | ||||||
chr18:12694137
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1117G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694137 | ||||||
chr18:12694138
|
A | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0118 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.804+1116T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694138 | ||||||
chr18:12694143
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1111C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694143 | ||||||
chr18:12694159
|
A | C | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1095T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694159 | ||||||
chr18:12694162
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1092G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694162 | ||||||
chr18:12694174
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1080G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694174 | ||||||
chr18:12694175
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1079T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694175 | ||||||
chr18:12694180
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1074T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694180 | ||||||
chr18:12694182
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1072T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694182 | ||||||
chr18:12694185
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1069G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694185 | ||||||
chr18:12694191
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1063T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694191 | ||||||
chr18:12694196
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1058T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694196 | ||||||
chr18:12694216
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1038T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694216 | ||||||
chr18:12694224
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1030T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694224 | ||||||
chr18:12694228
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1026T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694228 | ||||||
chr18:12694239
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1015T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694239 | ||||||
chr18:12694257
|
G | T | 1 | a0001c0001t0006g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.804+997C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694257 | ||||||
chr18:12694285
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.804+969A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694285 | ||||||
chr18:12694368
|
A | G | 1 | a0001c0001t0002g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804+886T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694368 | ||||||
chr18:12694380
|
G | A | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+874C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694380 | ||||||
chr18:12694530
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+724C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694530 | ||||||
chr18:12694708
|
C | CT | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | NA18940.hp2 NA19002.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+545dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694708 | ||||||
chr18:12694734
|
T | TG | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.804+519dupC | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694734 | ||||||
chr18:12694867
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.804+387G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694867 | ||||||
chr18:12694935
|
A | T | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+319T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694935 | ||||||
chr18:12694939
|
T | G | 1 | a0001c0001t0004g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.804+315A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694939 | ||||||
chr18:12694986
|
A | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+268T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694986 | ||||||
chr18:12694995
|
G | A | 22 | a0001c0001t0004g0009a0001c0001t0004g0033a0001c0001t0004g0056others(19): Show | 26 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.804+259C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694995 | ||||||
chr18:12694997
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.804+257C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694997 | ||||||
chr18:12695027
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.804+227G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12695027 | ||||||
chr18:12695087
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.804+167T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12695087 | ||||||
chr18:12695416
|
C | A | 39 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(36): Show | 58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.707-65G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695416 | ||||||
chr18:12695652
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0192a0005c0004t0001g0191 | 5 | HG01884.hp2 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-301T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695652 | ||||||
chr18:12695852
|
C | CCA | 79 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(76): Show | 97 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.707-503_707-502dup others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
C | CCACA | 46 | a0001c0001t0001g0032a0001c0001t0001g0166a0001c0001t0001g0167others(43): Show | 65 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.707-505_707-502dup others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
C | CCACACA | 11 | a0001c0001t0001g0063a0001c0001t0001g0083a0001c0001t0002g0038others(8): Show | 12 | HG01168.hp1 HG01928.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.707-507_707-502dup others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
C | CCACACAC others(1): Show |
11 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0085others(8): Show | 13 | HG00639.hp1 HG00741.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.707-509_707-502dup others(8): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
C | CCACACAC others(3): Show |
1 | a0001c0001t0001g0022 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.707-511_707-502dup others(10): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
CCA | C | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 26 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.707-503_707-502del others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
CCACACA | C | 13 | a0001c0001t0004g0009a0001c0001t0004g0180a0001c0001t0004g0181others(10): Show | 16 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.707-507_707-502del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695852
|
CCACACAC others(1): Show |
C | 5 | a0001c0001t0004g0033a0001c0001t0004g0177a0001c0001t0006g0059others(2): Show | 6 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-509_707-502del others(8): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | ||||||
chr18:12695867
|
C | G | 1 | a0001c0001t0006g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.707-516G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695867 | ||||||
chr18:12695886
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.707-535A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695886 | ||||||
chr18:12696124
|
G | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | NA18944.hp1 NA18969.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.707-773C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696124 | ||||||
chr18:12696232
|
G | A | 16 | a0001c0001t0004g0009a0001c0001t0004g0033a0001c0001t0004g0056others(13): Show | 20 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.707-881C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696232 | ||||||
chr18:12696449
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.706+774C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696449 | ||||||
chr18:12696502
|
A | AAAT | 7 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0059others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.706+718_706+720dup others(3): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696502 | ||||||
chr18:12696502
|
AAAT | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.706+718_706+720del others(3): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696502 | ||||||
chr18:12696502
|
AAATAAT | A | 17 | a0001c0001t0001g0176a0001c0001t0004g0009a0001c0001t0004g0033others(14): Show | 21 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.706+715_706+720del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696502 | ||||||
chr18:12696593
|
G | A | 1 | a0001c0001t0006g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.706+630C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696593 | ||||||
chr18:12696871
|
T | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0045others(14): Show | 24 | HG00609.hp1 HG01346.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.706+352A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696871 | ||||||
chr18:12696930
|
CTTATAT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.706+287_706+292del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696930 | ||||||
chr18:12696993
|
A | G | 2 | a0001c0001t0002g0198a0001c0001t0002g0199 | 2 | NA19065.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.706+230T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696993 | ||||||
chr18:12697082
|
T | G | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.706+141A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697082 | ||||||
chr18:12697084
|
A | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.706+139T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697084 | ||||||
chr18:12697109
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.706+114A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697109 | ||||||
chr18:12697207
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | NA18967.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.706+16T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697207 | ||||||
chr18:12697712
|
A | G | 72 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0010others(69): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.521-304T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697712 | ||||||
chr18:12697776
|
C | A | 1 | a0001c0001t0002g0252 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.521-368G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697776 | ||||||
chr18:12697796
|
T | C | 3 | a0001c0001t0002g0039a0001c0001t0002g0253a0001c0001t0002g0254 | 4 | HG02258.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-388A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697796 | ||||||
chr18:12697819
|
G | GC | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.521-412dupG | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697819 | ||||||
chr18:12697821
|
A | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.521-413T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697821 | ||||||
chr18:12697826
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.521-418C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697826 | ||||||
chr18:12697975
|
C | T | 1 | a0002c0002t0001g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.521-567G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697975 | ||||||
chr18:12698080
|
C | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0045others(14): Show | 24 | HG00609.hp1 HG01346.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.521-672G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698080 | ||||||
chr18:12698158
|
TTATTTA | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(10): Show | 14 | HG00639.hp1 HG02055.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.521-756_521-751del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698158 | ||||||
chr18:12698205
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.520+774A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698205 | ||||||
chr18:12698365
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 7 | HG02257.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.520+614G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698365 | ||||||
chr18:12698459
|
A | G | 1 | a0006c0006t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.520+520T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698459 | ||||||
chr18:12698607
|
C | T | 73 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(70): Show | 96 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.520+372G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698607 | ||||||
chr18:12699268
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.296-65A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 3/11 | chr18 | 12699268 | ||||||
chr18:12699287
|
C | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(8): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-84G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 3/11 | chr18 | 12699287 | ||||||
chr18:12699913
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | splice_region_variant&intron_variant | LOW | c.220-8C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12699913 | ||||||
chr18:12700093
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(281): Show | 371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.220-188T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700093 | ||||||
chr18:12700198
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.220-293A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700198 | ||||||
chr18:12700311
|
A | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0050others(3): Show | 7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-406T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700311 | ||||||
chr18:12700376
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220-471T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700376 | ||||||
chr18:12700513
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.219+445A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700513 | ||||||
chr18:12700690
|
C | A | 72 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0010others(69): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.219+268G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700690 | ||||||
chr18:12700850
|
G | A | 73 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(70): Show | 96 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.219+108C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700850 | ||||||
chr18:12700906
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.219+52C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700906 | ||||||
chr18:12700919
|
CATAT | C | 41 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0016others(38): Show | 60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.219+35_219+38delAT others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700919 | ||||||
chr18:12701327
|
A | C | 45 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.64-214T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701327 | ||||||
chr18:12701444
|
T | G | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-331A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701444 | ||||||
chr18:12701453
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.64-340C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701453 | ||||||
chr18:12701555
|
T | C | 1 | a0001c0001t0003g0290 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64-442A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701555 | ||||||
chr18:12701633
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-520T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701633 | ||||||
chr18:12701662
|
GCACT | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.64-553_64-550delAG others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701662 | ||||||
chr18:12701762
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-649T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701762 | ||||||
chr18:12701938
|
C | G | 73 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(70): Show | 96 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.63+548G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701938 | ||||||
chr18:12702081
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.63+405C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702081 | ||||||
chr18:12702124
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.63+362T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702124 | ||||||
chr18:12702146
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+340A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702146 | ||||||
chr18:12702218
|
C | T | 1 | a0001c0001t0006g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+268G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702218 | ||||||
chr18:12702374
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63+112T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702374 | ||||||
chr18:12702433
|
G | C | 1 | a0001c0001t0002g0040 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.63+53C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702433 |