geneid | 95681 |
---|---|
ensemblid | ENSG00000106477.20 |
hgncid | 12370 |
symbol | CEP41 |
name | centrosomal protein 41 |
refseq_nuc | NM_018718.3 |
refseq_prot | NP_061188.1 |
ensembl_nuc | ENST00000223208.10 |
ensembl_prot | ENSP00000223208.4 |
mane_status | MANE Select |
chr | chr7 |
start | 130393771 |
end | 130441016 |
strand | - |
ver | v1.2 |
region | chr7:130393771-130441016 |
region5000 | chr7:130388771-130446016 |
regionname0 | CEP41_chr7_130393771_130441016 |
regionname5000 | CEP41_chr7_130388771_130446016 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 373 | 343 | 82 | 69 | 138 | 14 | 38 | 106 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0002 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0003 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0004 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1122 | 342 | 82 | 69 | 137 | 14 | 38 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
c0002 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
c0003 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
c0004 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
c0005 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5171 | 46 | 2 | 15 | 24 | 1 | 4 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0002 | 0/0 | 5173 | 39 | 11 | 10 | 15 | 1 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0003 | 1/0 | 5171 | 25 | 12 | 3 | 4 | 3 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0004 | 0/0 | 5171 | 19 | 0 | 3 | 10 | 0 | 6 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0005 | 0/0 | 5172 | 12 | 0 | 2 | 10 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0006 | 0/0 | 5172 | 11 | 10 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0007 | 0/0 | 5172 | 11 | 1 | 2 | 4 | 0 | 4 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0008 | 0/0 | 5173 | 11 | 3 | 3 | 3 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0009 | 0/0 | 5172 | 10 | 0 | 3 | 0 | 4 | 3 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0010 | 0/0 | 5171 | 10 | 0 | 2 | 7 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0011 | 0/0 | 5172 | 8 | 0 | 3 | 3 | 1 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0012 | 0/0 | 5172 | 7 | 3 | 2 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0013 | 0/0 | 5168 | 6 | 0 | 1 | 5 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0014 | 0/0 | 5172 | 6 | 0 | 0 | 6 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0015 | 0/0 | 5174 | 5 | 1 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0016 | 0/0 | 5173 | 5 | 2 | 3 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0017 | 0/0 | 5171 | 5 | 0 | 2 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0018 | 0/0 | 5172 | 5 | 0 | 1 | 1 | 0 | 3 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0019 | 0/0 | 5171 | 4 | 4 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0020 | 0/0 | 5171 | 4 | 0 | 0 | 4 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0021 | 0/0 | 5174 | 4 | 0 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0022 | 0/0 | 5172 | 3 | 3 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0023 | 0/0 | 5173 | 3 | 3 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0024 | 0/0 | 5171 | 3 | 2 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0025 | 0/0 | 5170 | 3 | 1 | 0 | 1 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0026 | 0/0 | 5172 | 3 | 2 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0027 | 0/0 | 5171 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0028 | 0/0 | 5171 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0029 | 0/0 | 5171 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0030 | 0/0 | 5173 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0031 | 0/0 | 5170 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0032 | 0/0 | 5172 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0033 | 0/0 | 5173 | 2 | 0 | 2 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0034 | 0/0 | 5173 | 2 | 1 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0035 | 0/0 | 5172 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0036 | 0/0 | 5172 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0037 | 0/0 | 5172 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0038 | 0/0 | 5171 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0039 | 0/0 | 5172 | 2 | 0 | 0 | 1 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0040 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0041 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0042 | 0/0 | 5173 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0043 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0044 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0045 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0046 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0047 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0048 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0049 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0050 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0051 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0052 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0053 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0054 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0055 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0056 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0057 | 0/0 | 5171 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0058 | 0/0 | 5171 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0059 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0060 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0061 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0062 | 0/0 | 5161 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0063 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0064 | 0/1 | 5171 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0065 | 0/0 | 5170 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0066 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0067 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0068 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0069 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0070 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0071 | 0/0 | 5172 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0072 | 0/0 | 5171 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0073 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0074 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0075 | 0/0 | 5171 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0076 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0077 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0078 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0079 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0080 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0081 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0082 | 0/0 | 5170 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0083 | 0/0 | 5170 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0084 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0085 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0086 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0087 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0088 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
t0089 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0015 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1122 | 342 | 82 | 69 | 137 | 14 | 38 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0005 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0002c0002 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0003c0004 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0004c0003 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6292 | 45 | 2 | 15 | 23 | 1 | 4 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0002 | 0/0 | 6294 | 39 | 11 | 10 | 15 | 1 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0003 | 1/0 | 6292 | 25 | 12 | 3 | 4 | 3 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0004 | 0/0 | 6292 | 19 | 0 | 3 | 10 | 0 | 6 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0005 | 0/0 | 6293 | 11 | 0 | 1 | 10 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0006 | 0/0 | 6293 | 11 | 10 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0007 | 0/0 | 6293 | 11 | 1 | 2 | 4 | 0 | 4 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0008 | 0/0 | 6294 | 11 | 3 | 3 | 3 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0009 | 0/0 | 6293 | 10 | 0 | 3 | 0 | 4 | 3 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0010 | 0/0 | 6292 | 10 | 0 | 2 | 7 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0011 | 0/0 | 6293 | 8 | 0 | 3 | 3 | 1 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0012 | 0/0 | 6293 | 7 | 3 | 2 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0013 | 0/0 | 6289 | 6 | 0 | 1 | 5 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0014 | 0/0 | 6293 | 6 | 0 | 0 | 6 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0015 | 0/0 | 6295 | 5 | 1 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0016 | 0/0 | 6294 | 5 | 2 | 3 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0017 | 0/0 | 6292 | 5 | 0 | 2 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0018 | 0/0 | 6293 | 5 | 0 | 1 | 1 | 0 | 3 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0019 | 0/0 | 6292 | 4 | 4 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0020 | 0/0 | 6292 | 4 | 0 | 0 | 4 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0021 | 0/0 | 6295 | 4 | 0 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0022 | 0/0 | 6293 | 3 | 3 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0023 | 0/0 | 6294 | 3 | 3 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0024 | 0/0 | 6292 | 3 | 2 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0025 | 0/0 | 6291 | 3 | 1 | 0 | 1 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0026 | 0/0 | 6293 | 3 | 2 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0027 | 0/0 | 6292 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0028 | 0/0 | 6292 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0029 | 0/0 | 6292 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0030 | 0/0 | 6294 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0031 | 0/0 | 6291 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0032 | 0/0 | 6293 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0033 | 0/0 | 6294 | 2 | 0 | 2 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0034 | 0/0 | 6294 | 2 | 1 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0035 | 0/0 | 6293 | 2 | 0 | 1 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0036 | 0/0 | 6293 | 2 | 2 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0037 | 0/0 | 6293 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0038 | 0/0 | 6292 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0039 | 0/0 | 6293 | 2 | 0 | 0 | 1 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0040 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0041 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0042 | 0/0 | 6294 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0043 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0044 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0045 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0046 | 0/0 | 6293 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0047 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0048 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0049 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0050 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0051 | 0/0 | 6291 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0052 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0053 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0054 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0055 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0056 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0057 | 0/0 | 6292 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0058 | 0/0 | 6292 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0059 | 0/0 | 6293 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0060 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0061 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0062 | 0/0 | 6282 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0063 | 0/0 | 6293 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0064 | 0/1 | 6292 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0065 | 0/0 | 6291 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0066 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0068 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0069 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0070 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0071 | 0/0 | 6293 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0072 | 0/0 | 6292 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0073 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0074 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0075 | 0/0 | 6292 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0076 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0077 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0078 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0079 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0080 | 0/0 | 6293 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0082 | 0/0 | 6291 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0083 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0084 | 0/0 | 6293 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0085 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0086 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0087 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0088 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0001t0089 | 0/0 | 6335 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0001c0005t0001 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0002c0002t0005 | 0/0 | 6293 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0003c0004t0081 | 0/0 | 6291 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
a0004c0003t0067 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | copy fasta | chr7 | 130388771 | 130446016 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0015 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0010g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0010g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0010g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0011g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0013g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0013g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0013g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0014g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0014g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0014g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0014g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0015g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0015g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0015g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0016g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0016g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0017g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0017g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0017g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0018g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0018g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0018g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0018g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0018g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0019g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0019g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0020g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0020g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0021g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0021g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0021g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0022g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0022g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0022g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0023g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0023g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0023g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0024g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0024g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0025g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0025g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0025g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0026g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0026g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0026g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0027g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0027g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0027g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0028g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0028g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0029g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0029g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0030g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0030g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0031g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0031g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0032g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0032g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0033g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0033g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0034g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0034g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0035g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0035g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0036g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0036g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0037g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0037g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0038g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0038g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0039g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0039g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0040g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0041g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0042g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0043g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0044g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0045g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0046g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0047g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0048g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0049g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0050g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0051g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0052g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0053g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0054g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0055g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0056g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0057g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0058g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0059g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0060g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0061g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0062g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0063g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0064g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0065g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0066g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0068g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0069g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0070g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0071g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0072g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0073g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0074g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0075g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0076g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0077g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0078g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0079g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0080g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0082g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0083g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0084g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0085g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0086g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0087g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0088g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0001t0089g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0001c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0003c0004t0081g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
a0004c0003t0067g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0071 | g0298 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00099 | hp2 | a0001 | c0001 | t0009 | g0110 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0125 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00140 | hp2 | a0001 | c0001 | t0011 | g0092 | EUR | GBR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00280 | hp1 | a0001 | c0001 | t0059 | g0089 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00280 | hp2 | a0001 | c0001 | t0009 | g0108 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00323 | hp2 | a0001 | c0001 | t0058 | g0109 | EUR | FIN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00408 | hp1 | a0001 | c0001 | t0089 | g0310 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00438 | hp1 | a0001 | c0001 | t0079 | g0257 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0279 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00558 | hp1 | a0001 | c0001 | t0021 | g0020 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00558 | hp2 | a0001 | c0001 | t0013 | g0028 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00597 | hp1 | a0001 | c0001 | t0011 | g0134 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00621 | hp1 | a0001 | c0001 | t0035 | g0268 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00621 | hp2 | a0001 | c0001 | t0011 | g0131 | EAS | CHS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0128 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00733 | hp1 | a0001 | c0001 | t0033 | g0212 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01070 | hp1 | a0001 | c0001 | t0017 | g0019 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01071 | hp1 | a0001 | c0001 | t0017 | g0019 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0087 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01081 | hp2 | a0001 | c0001 | t0009 | g0088 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0282 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0261 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0266 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01168 | hp1 | a0001 | c0001 | t0011 | g0180 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01175 | hp1 | a0001 | c0001 | t0042 | g0155 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01192 | hp1 | a0001 | c0001 | t0072 | g0243 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01192 | hp2 | a0001 | c0001 | t0016 | g0113 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0106 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01256 | hp1 | a0001 | c0001 | t0009 | g0090 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01256 | hp2 | a0001 | c0001 | t0021 | g0210 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01257 | hp1 | a0001 | c0001 | t0065 | g0286 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0213 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01261 | hp1 | a0001 | c0001 | t0012 | g0146 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01346 | hp2 | a0001 | c0001 | t0062 | g0100 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01358 | hp1 | a0001 | c0001 | t0084 | g0241 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01361 | hp1 | a0001 | c0001 | t0030 | g0135 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01361 | hp2 | a0001 | c0001 | t0018 | g0188 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0013 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0152 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01517 | hp1 | a0001 | c0001 | t0009 | g0013 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01517 | hp2 | a0001 | c0001 | t0025 | g0281 | EUR | IBS | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01884 | hp1 | a0001 | c0001 | t0031 | g0149 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01884 | hp2 | a0001 | c0001 | t0022 | g0171 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01891 | hp1 | a0001 | c0001 | t0024 | g0011 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01891 | hp2 | a0001 | c0001 | t0068 | g0292 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01934 | hp1 | a0001 | c0001 | t0013 | g0029 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01943 | hp1 | a0001 | c0001 | t0024 | g0011 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0116 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01978 | hp2 | a0001 | c0001 | t0063 | g0093 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01993 | hp1 | a0001 | c0001 | t0008 | g0209 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01993 | hp2 | a0001 | c0001 | t0026 | g0305 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02004 | hp1 | a0001 | c0001 | t0033 | g0181 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02004 | hp2 | a0002 | c0002 | t0005 | g0074 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02055 | hp2 | a0004 | c0003 | t0067 | g0309 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02056 | hp1 | a0001 | c0001 | t0015 | g0040 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02056 | hp2 | a0001 | c0001 | t0030 | g0132 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02074 | hp2 | a0001 | c0001 | t0040 | g0154 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02080 | hp2 | a0001 | c0001 | t0039 | g0207 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0214 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02135 | hp2 | a0001 | c0001 | t0011 | g0137 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02148 | hp1 | a0001 | c0001 | t0012 | g0075 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02148 | hp2 | a0001 | c0001 | t0015 | g0053 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02165 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | CDX | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0117 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02273 | hp2 | a0001 | c0001 | t0035 | g0239 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02523 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | KHV | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02572 | hp1 | a0001 | c0001 | t0056 | g0026 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0072 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02615 | hp1 | a0001 | c0001 | t0044 | g0121 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02615 | hp2 | a0001 | c0001 | t0034 | g0304 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0307 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02698 | hp1 | a0001 | c0001 | t0007 | g0258 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02698 | hp2 | a0001 | c0001 | t0009 | g0107 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02717 | hp1 | a0001 | c0001 | t0048 | g0027 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0291 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02738 | hp2 | a0001 | c0001 | t0018 | g0280 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02809 | hp2 | a0001 | c0001 | t0023 | g0179 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02818 | hp2 | a0001 | c0001 | t0019 | g0157 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02886 | hp1 | a0001 | c0001 | t0026 | g0303 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0163 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02896 | hp1 | a0001 | c0001 | t0023 | g0085 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02896 | hp2 | a0001 | c0001 | t0031 | g0066 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02897 | hp1 | a0001 | c0001 | t0023 | g0084 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02922 | hp1 | a0001 | c0001 | t0060 | g0025 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02965 | hp2 | a0001 | c0001 | t0026 | g0308 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02970 | hp2 | a0001 | c0001 | t0036 | g0294 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02976 | hp2 | a0001 | c0001 | t0045 | g0060 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0256 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03041 | hp2 | a0001 | c0001 | t0055 | g0024 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03098 | hp1 | a0001 | c0001 | t0022 | g0172 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03098 | hp2 | a0001 | c0001 | t0066 | g0290 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0297 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03195 | hp1 | a0001 | c0001 | t0015 | g0095 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03195 | hp2 | a0001 | c0001 | t0036 | g0293 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03209 | hp1 | a0001 | c0001 | t0050 | g0022 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0306 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03225 | hp1 | a0001 | c0001 | t0076 | g0288 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03490 | hp1 | a0001 | c0001 | t0037 | g0300 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0006 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03491 | hp2 | a0001 | c0001 | t0057 | g0136 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0006 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03492 | hp2 | a0001 | c0001 | t0037 | g0301 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03516 | hp2 | a0001 | c0001 | t0029 | g0167 | AFR | ESN | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03540 | hp2 | a0001 | c0001 | t0024 | g0067 | AFR | GWD | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0099 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0032 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03688 | hp2 | a0001 | c0001 | t0038 | g0253 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0119 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03710 | hp1 | a0001 | c0001 | t0034 | g0272 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03710 | hp2 | a0001 | c0001 | t0046 | g0081 | SAS | PJL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03831 | hp1 | a0001 | c0001 | t0018 | g0202 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03834 | hp1 | a0001 | c0001 | t0011 | g0115 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03834 | hp2 | a0001 | c0001 | t0082 | g0236 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03927 | hp2 | a0001 | c0001 | t0018 | g0200 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03942 | hp2 | a0001 | c0001 | t0038 | g0246 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0299 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04184 | hp2 | a0001 | c0001 | t0039 | g0208 | SAS | BEB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0273 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04199 | hp2 | a0001 | c0001 | t0075 | g0270 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04228 | hp1 | a0001 | c0001 | t0009 | g0114 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG04228 | hp2 | a0001 | c0001 | t0008 | g0206 | SAS | STU | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18522 | hp2 | a0001 | c0001 | t0054 | g0023 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18747 | hp1 | a0001 | c0001 | t0020 | g0014 | EAS | CHB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18747 | hp2 | a0001 | c0001 | t0061 | g0133 | EAS | CHB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18943 | hp1 | a0001 | c0001 | t0078 | g0277 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18943 | hp2 | a0001 | c0005 | t0001 | g0284 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18944 | hp1 | a0001 | c0001 | t0021 | g0020 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18944 | hp2 | a0001 | c0001 | t0014 | g0186 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18945 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18949 | hp1 | a0001 | c0001 | t0012 | g0124 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18949 | hp2 | a0001 | c0001 | t0032 | g0127 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18950 | hp1 | a0001 | c0001 | t0012 | g0076 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18950 | hp2 | a0001 | c0001 | t0017 | g0244 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18954 | hp2 | a0001 | c0001 | t0047 | g0054 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18959 | hp1 | a0001 | c0001 | t0025 | g0249 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18959 | hp2 | a0001 | c0001 | t0010 | g0031 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18962 | hp1 | a0001 | c0001 | t0080 | g0215 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18962 | hp2 | a0001 | c0001 | t0027 | g0276 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18964 | hp2 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18969 | hp2 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18972 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18972 | hp2 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18978 | hp1 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18978 | hp2 | a0001 | c0001 | t0049 | g0062 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18982 | hp1 | a0001 | c0001 | t0027 | g0275 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18982 | hp2 | a0001 | c0001 | t0020 | g0122 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18983 | hp2 | a0001 | c0001 | t0013 | g0168 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18984 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18984 | hp2 | a0001 | c0001 | t0074 | g0218 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18986 | hp2 | a0001 | c0001 | t0032 | g0033 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18987 | hp1 | a0001 | c0001 | t0041 | g0144 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18987 | hp2 | a0001 | c0001 | t0014 | g0233 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18990 | hp1 | a0001 | c0001 | t0083 | g0201 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18994 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18994 | hp2 | a0001 | c0001 | t0020 | g0014 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18999 | hp1 | a0001 | c0001 | t0014 | g0228 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA18999 | hp2 | a0001 | c0001 | t0086 | g0283 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19000 | hp1 | a0001 | c0001 | t0014 | g0285 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19000 | hp2 | a0001 | c0001 | t0053 | g0165 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19003 | hp1 | a0001 | c0001 | t0017 | g0230 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19003 | hp2 | a0001 | c0001 | t0052 | g0042 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19004 | hp2 | a0001 | c0001 | t0017 | g0229 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19007 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19009 | hp1 | a0001 | c0001 | t0027 | g0278 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19009 | hp2 | a0001 | c0001 | t0077 | g0264 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19030 | hp2 | a0001 | c0001 | t0043 | g0059 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19043 | hp1 | a0003 | c0004 | t0081 | g0296 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19043 | hp2 | a0001 | c0001 | t0022 | g0170 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19060 | hp1 | a0001 | c0001 | t0069 | g0211 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19062 | hp1 | a0001 | c0001 | t0028 | g0017 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19064 | hp1 | a0001 | c0001 | t0028 | g0017 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19064 | hp2 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19065 | hp1 | a0001 | c0001 | t0021 | g0216 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19068 | hp2 | a0001 | c0001 | t0088 | g0238 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19072 | hp2 | a0001 | c0001 | t0070 | g0189 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19074 | hp1 | a0001 | c0001 | t0014 | g0248 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19078 | hp2 | a0001 | c0001 | t0015 | g0061 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19079 | hp1 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19079 | hp2 | a0001 | c0001 | t0085 | g0235 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19080 | hp2 | a0001 | c0001 | t0018 | g0191 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19082 | hp1 | a0001 | c0001 | t0028 | g0197 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0056 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19090 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | JPT | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | YRI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ASW | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA20129 | hp2 | a0001 | c0001 | t0087 | g0295 | AFR | ASW | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0071 | EUR | TSI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01123 | hp1 | a0001 | c0001 | t0016 | g0035 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0083 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02486 | hp1 | a0001 | c0001 | t0073 | g0289 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0164 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02559 | hp1 | a0001 | c0001 | t0051 | g0178 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG02559 | hp2 | a0001 | c0001 | t0025 | g0182 | AFR | ACB | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | MSL | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | USA | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | USA | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA21309 | hp1 | a0001 | c0001 | t0019 | g0145 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
NA21309 | hp2 | a0001 | c0001 | t0029 | g0166 | AFR | LWK | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0064 | g0274 | REF | REF | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0015 | REF | REF | CEP41_chr7_130388771_130446016 | CEP41 | chr7 | 130388771 | 130446016 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:130398948
|
G | C | 1 | a0003 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1065C>G | p.Ser355Arg | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1115/6292 | 1065/1122 | 355/373 | chr7 | 130398948 | ||
chr7:130400746
|
A | C | 1 | a0004 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.718T>G | p.Cys240Gly | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/11 | 768/6292 | 718/1122 | 240/373 | chr7 | 130400746 | ||
chr7:130404579
|
C | T | 1 | a0002 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.407G>A | p.Arg136His | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/11 | 457/6292 | 407/1122 | 136/373 | chr7 | 130404579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:130412181
|
G | A | 1 | a0001c0005 | 1 | NA18943.hp2 | splice_region_variant&synonymous_variant | LOW | c.205C>T | p.Leu69Leu | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/11 | 255/6292 | 205/1122 | 69/373 | chr7 | 130412181 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:130393789
|
C | T | 60 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(57): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*5102G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 5102 | chr7 | 130393789 | |||||
chr7:130393826
|
C | CT | 2 | a0001c0001t0013a0001c0001t0066 | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5064dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 5064 | chr7 | 130393826 | |||||
chr7:130393833
|
C | A | 1 | a0001c0001t0056 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5058G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 5058 | chr7 | 130393833 | |||||
chr7:130393897
|
A | G | 1 | a0001c0001t0075 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4994T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4994 | chr7 | 130393897 | |||||
chr7:130394296
|
C | T | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4595G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4595 | chr7 | 130394296 | |||||
chr7:130394297
|
G | A | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4594C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4594 | chr7 | 130394297 | |||||
chr7:130394577
|
A | G | 1 | a0001c0001t0022 | 3 | HG01884.hp2 HG03098.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4314T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4314 | chr7 | 130394577 | |||||
chr7:130394596
|
C | G | 33 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(30): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4295G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4295 | chr7 | 130394596 | |||||
chr7:130394645
|
A | G | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4246T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4246 | chr7 | 130394645 | |||||
chr7:130394675
|
G | A | 1 | a0001c0001t0042 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4216C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4216 | chr7 | 130394675 | |||||
chr7:130394700
|
G | C | 1 | a0001c0001t0048 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4191C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4191 | chr7 | 130394700 | |||||
chr7:130394776
|
T | C | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4115A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4115 | chr7 | 130394776 | |||||
chr7:130394854
|
T | C | 17 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(14): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4037A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 4037 | chr7 | 130394854 | |||||
chr7:130394963
|
G | A | 2 | a0001c0001t0073a0001c0001t0076 | 2 | HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3928C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3928 | chr7 | 130394963 | |||||
chr7:130394981
|
G | C | 1 | a0001c0001t0049 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3910C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3910 | chr7 | 130394981 | |||||
chr7:130394983
|
G | A | 1 | a0001c0001t0077 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3908C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3908 | chr7 | 130394983 | |||||
chr7:130395004
|
G | C | 12 | a0001c0001t0004a0001c0001t0010a0001c0001t0018others(9): Show | 49 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3887C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3887 | chr7 | 130395004 | |||||
chr7:130395108
|
A | G | 1 | a0001c0001t0033 | 2 | HG00733.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3783T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3783 | chr7 | 130395108 | |||||
chr7:130395126
|
C | A | 2 | a0001c0001t0037a0001c0001t0071 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3765G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3765 | chr7 | 130395126 | |||||
chr7:130395140
|
C | T | 1 | a0001c0001t0074 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3751G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3751 | chr7 | 130395140 | |||||
chr7:130395350
|
C | T | 1 | a0001c0001t0073 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3541G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3541 | chr7 | 130395350 | |||||
chr7:130395364
|
G | GA | 38 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(35): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*3526dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3526 | chr7 | 130395364 | |||||
chr7:130395384
|
G | A | 2 | a0001c0001t0037a0001c0001t0071 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3507C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3507 | chr7 | 130395384 | |||||
chr7:130395447
|
G | T | 1 | a0001c0001t0024 | 3 | HG01891.hp1 HG01943.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3444C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3444 | chr7 | 130395447 | |||||
chr7:130395698
|
G | A | 1 | a0001c0001t0028 | 3 | NA19062.hp1 NA19064.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3193C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3193 | chr7 | 130395698 | |||||
chr7:130395880
|
T | TA | 8 | a0001c0001t0004a0001c0001t0010a0001c0001t0018others(5): Show | 44 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3010dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3010 | chr7 | 130395880 | |||||
chr7:130395880
|
TA | T | 6 | a0001c0001t0025a0001c0001t0031a0001c0001t0051others(3): Show | 9 | HG00323.hp2 HG01517.hp2 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3010delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 3010 | chr7 | 130395880 | |||||
chr7:130395995
|
C | T | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2896G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2896 | chr7 | 130395995 | |||||
chr7:130396012
|
T | C | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2879A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2879 | chr7 | 130396012 | |||||
chr7:130396079
|
C | T | 1 | a0001c0001t0066 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2812G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2812 | chr7 | 130396079 | |||||
chr7:130396409
|
T | A | 5 | a0001c0001t0035a0001c0001t0053a0001c0001t0079others(2): Show | 6 | HG00438.hp1 HG00621.hp1 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2482A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2482 | chr7 | 130396409 | |||||
chr7:130396410
|
A | T | 1 | a0001c0001t0038 | 2 | HG03688.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2481T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2481 | chr7 | 130396410 | |||||
chr7:130396477
|
C | T | 1 | a0001c0001t0047 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2414G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2414 | chr7 | 130396477 | |||||
chr7:130396527
|
C | T | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2364 | chr7 | 130396527 | |||||
chr7:130396665
|
C | T | 1 | a0001c0001t0054 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2226G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2226 | chr7 | 130396665 | |||||
chr7:130396775
|
A | G | 1 | a0001c0001t0045 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2116 | chr7 | 130396775 | |||||
chr7:130396850
|
C | T | 22 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(19): Show | 58 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2041 | chr7 | 130396850 | |||||
chr7:130396868
|
T | C | 1 | a0001c0001t0080 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 2023 | chr7 | 130396868 | |||||
chr7:130396960
|
G | A | 14 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(11): Show | 48 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1931C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1931 | chr7 | 130396960 | |||||
chr7:130396991
|
C | T | 1 | a0001c0001t0072 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1900G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1900 | chr7 | 130396991 | |||||
chr7:130397032
|
C | A | 19 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(16): Show | 53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1859 | chr7 | 130397032 | |||||
chr7:130397245
|
C | T | 1 | a0001c0001t0069 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1646G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1646 | chr7 | 130397245 | |||||
chr7:130397247
|
T | C | 1 | a0001c0001t0043 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1644A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1644 | chr7 | 130397247 | |||||
chr7:130397324
|
T | G | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1567A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1567 | chr7 | 130397324 | |||||
chr7:130397351
|
T | C | 1 | a0001c0001t0044 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1540A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1540 | chr7 | 130397351 | |||||
chr7:130397357
|
A | G | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1534T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1534 | chr7 | 130397357 | |||||
chr7:130397379
|
G | A | 2 | a0001c0001t0036a0001c0001t0068 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1512C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1512 | chr7 | 130397379 | |||||
chr7:130397506
|
A | AT | 25 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(22): Show | 117 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1384dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1384 | chr7 | 130397506 | |||||
chr7:130397506
|
A | ATT | 10 | a0001c0001t0015a0001c0001t0021a0001c0001t0041others(7): Show | 17 | HG00558.hp1 HG01175.hp1 HG01256.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1383_*1384dupAA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1384 | chr7 | 130397506 | |||||
chr7:130397506
|
A | C | 1 | a0001c0001t0071 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1385T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1385 | chr7 | 130397506 | |||||
chr7:130397506
|
AT | A | 10 | a0001c0001t0004a0001c0001t0010a0001c0001t0027others(7): Show | 41 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1384delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1384 | chr7 | 130397506 | |||||
chr7:130397506
|
ATTTT | A | 1 | a0001c0001t0013 | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1381_*1384delAAAA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1381 | chr7 | 130397506 | |||||
chr7:130397506
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0062 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374_*1384delAAAA others(7): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1374 | chr7 | 130397506 | |||||
chr7:130397702
|
G | A | 1 | a0001c0001t0084 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1189C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 1189 | chr7 | 130397702 | |||||
chr7:130397964
|
A | G | 2 | a0001c0001t0064a0001c0001t0065 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 927 | chr7 | 130397964 | |||||
chr7:130397972
|
G | A | 1 | a0001c0001t0063 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*919C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 919 | chr7 | 130397972 | |||||
chr7:130398086
|
T | C | 3 | a0001c0001t0020a0001c0001t0085a0001c0001t0086 | 6 | NA18747.hp1 NA18982.hp2 NA18994.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*805A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 805 | chr7 | 130398086 | |||||
chr7:130398115
|
C | T | 1 | a0001c0001t0040 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 776 | chr7 | 130398115 | |||||
chr7:130398236
|
G | A | 2 | a0001c0001t0013a0001c0001t0029 | 8 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*655C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 655 | chr7 | 130398236 | |||||
chr7:130398508
|
G | A | 1 | a0001c0001t0087 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 383 | chr7 | 130398508 | |||||
chr7:130398748
|
G | C | 1 | a0001c0001t0088 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 143 | chr7 | 130398748 | |||||
chr7:130398806
|
G | T | 1 | a0001c0001t0029 | 2 | HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*85C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 11/11 | 85 | chr7 | 130398806 | |||||
chr7:130440971
|
T | G | 46 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(43): Show | 159 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
5_prime_UTR_variant | MODIFIER | c.-5A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/11 | 5 | chr7 | 130440971 | |||||
chr7:130440986
|
G | GTTCGGGG others(36): Show |
1 | a0001c0001t0089 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63_-21dupGGAAGCTA others(35): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/11 | 21 | chr7 | 130440986 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:130399187
|
G | GGCCT | 37 | a0001c0001t0004g0005a0001c0001t0004g0018a0001c0001t0004g0184others(34): Show | 45 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.974-152_974-149dup others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399187 | ||||||
chr7:130399426
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-387G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399426 | ||||||
chr7:130399544
|
G | A | 2 | a0001c0001t0002g0097a0001c0001t0016g0116 | 2 | HG01978.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.973+495C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399544 | ||||||
chr7:130399654
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.973+385G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399654 | ||||||
chr7:130399734
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.973+305G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399734 | ||||||
chr7:130399819
|
C | CA | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(169): Show | 199 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.973+219dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399819 | ||||||
chr7:130399819
|
C | CAA | 119 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(116): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.973+218_973+219dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399819 | ||||||
chr7:130399819
|
C | CAAA | 6 | a0001c0001t0006g0111a0001c0001t0006g0112a0001c0001t0036g0293others(3): Show | 6 | HG01346.hp2 HG01891.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+217_973+219dup others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399819 | ||||||
chr7:130399833
|
G | A | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.973+206C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399833 | ||||||
chr7:130399835
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.973+204G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 10/10 | chr7 | 130399835 | ||||||
chr7:130400408
|
A | T | 1 | a0001c0001t0003g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.758-154T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/10 | chr7 | 130400408 | ||||||
chr7:130400510
|
A | C | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.757+197T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/10 | chr7 | 130400510 | ||||||
chr7:130400604
|
T | C | 1 | a0001c0001t0032g0033 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.757+103A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 9/10 | chr7 | 130400604 | ||||||
chr7:130400987
|
T | G | 15 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(12): Show | 16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-166A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130400987 | ||||||
chr7:130401119
|
T | A | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.643-298A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401119 | ||||||
chr7:130401325
|
G | A | 7 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(4): Show | 8 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-504C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401325 | ||||||
chr7:130401325
|
G | C | 15 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(12): Show | 16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-504C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401325 | ||||||
chr7:130401365
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.642+516A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401365 | ||||||
chr7:130401467
|
TATAAG | T | 123 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(120): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.642+409_642+413del others(5): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401467 | ||||||
chr7:130401656
|
T | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+225A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401656 | ||||||
chr7:130401797
|
T | C | 7 | a0001c0001t0005g0098a0001c0001t0014g0228a0001c0001t0014g0233others(4): Show | 7 | HG01243.hp1 NA18950.hp2 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+84A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 8/10 | chr7 | 130401797 | ||||||
chr7:130402251
|
T | C | 1 | a0001c0001t0039g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.575-303A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402251 | ||||||
chr7:130402335
|
G | C | 1 | a0001c0001t0043g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+313C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402335 | ||||||
chr7:130402343
|
C | CA | 44 | a0001c0001t0002g0051a0001c0001t0005g0130a0001c0001t0005g0156others(41): Show | 46 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.574+304dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402343 | ||||||
chr7:130402343
|
C | CAA | 13 | a0001c0001t0003g0078a0001c0001t0006g0103a0001c0001t0009g0106others(10): Show | 14 | HG00099.hp1 HG00558.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.574+303_574+304dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402343 | ||||||
chr7:130402345
|
A | AC | 5 | a0001c0001t0006g0111a0001c0001t0006g0112a0001c0001t0016g0113others(2): Show | 5 | HG01192.hp2 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.574+302_574+303ins others(1): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402345 | ||||||
chr7:130402353
|
AC | A | 48 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(45): Show | 56 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.574+294delG | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402353 | ||||||
chr7:130402354
|
C | A | 146 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(143): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.574+294G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402354 | ||||||
chr7:130402379
|
A | G | 1 | a0001c0001t0031g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574+269T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402379 | ||||||
chr7:130402418
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.574+230C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402418 | ||||||
chr7:130402606
|
T | C | 1 | a0001c0001t0014g0233 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.574+42A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402606 | ||||||
chr7:130402607
|
G | T | 1 | a0001c0001t0014g0233 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.574+41C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 7/10 | chr7 | 130402607 | ||||||
chr7:130402833
|
T | C | 1 | a0001c0001t0008g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.423-34A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402833 | ||||||
chr7:130402856
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-57G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402856 | ||||||
chr7:130402906
|
G | A | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.423-107C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402906 | ||||||
chr7:130402910
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-111C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402910 | ||||||
chr7:130402934
|
C | T | 6 | a0001c0001t0002g0139a0001c0001t0013g0007a0001c0001t0013g0028others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-135G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130402934 | ||||||
chr7:130403043
|
C | T | 1 | a0001c0001t0014g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.423-244G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403043 | ||||||
chr7:130403048
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.423-249G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403048 | ||||||
chr7:130403139
|
G | A | 57 | a0001c0001t0003g0078a0001c0001t0005g0130a0001c0001t0006g0012others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.423-340C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403139 | ||||||
chr7:130403258
|
C | T | 6 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0064g0274others(3): Show | 6 | HG01257.hp1 HG01891.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-459G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403258 | ||||||
chr7:130403299
|
C | T | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-500G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403299 | ||||||
chr7:130403301
|
T | G | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-502A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403301 | ||||||
chr7:130403303
|
C | G | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-504G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403303 | ||||||
chr7:130403304
|
A | T | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-505T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403304 | ||||||
chr7:130403305
|
T | A | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.423-506A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403305 | ||||||
chr7:130403350
|
T | A | 1 | a0001c0001t0038g0246 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.423-551A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403350 | ||||||
chr7:130403360
|
T | G | 1 | a0001c0001t0051g0178 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.423-561A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403360 | ||||||
chr7:130403550
|
C | T | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.423-751G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403550 | ||||||
chr7:130403671
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-872C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403671 | ||||||
chr7:130403724
|
A | G | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.422+840T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403724 | ||||||
chr7:130403770
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.422+794C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403770 | ||||||
chr7:130403772
|
A | T | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+792T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403772 | ||||||
chr7:130403773
|
A | G | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+791T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403773 | ||||||
chr7:130403774
|
C | T | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+790G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403774 | ||||||
chr7:130403776
|
G | C | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422+788C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403776 | ||||||
chr7:130403837
|
G | A | 1 | a0001c0001t0005g0148 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.422+727C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130403837 | ||||||
chr7:130404089
|
A | G | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422+475T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130404089 | ||||||
chr7:130404196
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422+368C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130404196 | ||||||
chr7:130404322
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.422+242G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 6/10 | chr7 | 130404322 | ||||||
chr7:130404810
|
A | G | 2 | a0001c0001t0009g0088a0001c0001t0009g0090 | 2 | HG01081.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.278-102T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130404810 | ||||||
chr7:130405194
|
G | A | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-486C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405194 | ||||||
chr7:130405221
|
G | A | 2 | a0001c0001t0073g0289a0001c0001t0076g0288 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.278-513C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405221 | ||||||
chr7:130405229
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-521G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405229 | ||||||
chr7:130405836
|
A | G | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-1128T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405836 | ||||||
chr7:130405842
|
G | A | 199 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(196): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.278-1134C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405842 | ||||||
chr7:130405922
|
G | A | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.278-1214C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130405922 | ||||||
chr7:130406110
|
TAATA | T | 108 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(105): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.278-1406_278-1403d others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406110 | ||||||
chr7:130406278
|
G | GT | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-1571dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406278 | ||||||
chr7:130406285
|
T | A | 3 | a0001c0001t0023g0084a0001c0001t0023g0085a0001c0001t0034g0304 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.278-1577A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406285 | ||||||
chr7:130406305
|
C | T | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.278-1597G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406305 | ||||||
chr7:130406417
|
C | T | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.278-1709G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406417 | ||||||
chr7:130406514
|
G | A | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.278-1806C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406514 | ||||||
chr7:130406824
|
T | TG | 8 | a0001c0001t0001g0265a0001c0001t0002g0045a0001c0001t0002g0086others(5): Show | 8 | HG00140.hp2 HG01261.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-2117dupC | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406824 | ||||||
chr7:130406829
|
G | GA | 6 | a0001c0001t0002g0043a0001c0001t0002g0175a0001c0001t0006g0112others(3): Show | 6 | HG02258.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2122_278-2121i others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406829 | ||||||
chr7:130406832
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2124G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406832 | ||||||
chr7:130406928
|
G | C | 200 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(197): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.278-2220C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406928 | ||||||
chr7:130406964
|
A | G | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2256T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406964 | ||||||
chr7:130406989
|
T | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2281A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130406989 | ||||||
chr7:130407206
|
G | A | 70 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(67): Show | 79 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.278-2498C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407206 | ||||||
chr7:130407219
|
A | T | 1 | a0001c0001t0018g0188 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.278-2511T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407219 | ||||||
chr7:130407253
|
A | AAC | 23 | a0001c0001t0001g0254a0001c0001t0003g0151a0001c0001t0005g0130others(20): Show | 23 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.278-2547_278-2546d others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
A | AACAC | 7 | a0001c0001t0001g0219a0001c0001t0035g0239a0001c0001t0035g0268others(4): Show | 7 | HG00438.hp1 HG00621.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-2549_278-2546d others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
A | AACACAC | 4 | a0001c0001t0016g0099a0001c0001t0016g0116a0001c0001t0022g0172others(1): Show | 4 | HG01978.hp1 HG01978.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2551_278-2546d others(8): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
AAC | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(164): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.278-2547_278-2546d others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
AACAC | A | 26 | a0001c0001t0001g0227a0001c0001t0001g0287a0001c0001t0001g0302others(23): Show | 26 | HG00733.hp1 HG00738.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.278-2549_278-2546d others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
AACACAC | A | 14 | a0001c0001t0001g0224a0001c0001t0001g0269a0001c0001t0002g0049others(11): Show | 14 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.278-2551_278-2546d others(8): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
AACACACA others(1): Show |
A | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-2553_278-2546d others(10): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407253
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0002g0041a0003c0004t0081g0296 | 2 | HG02523.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.278-2555_278-2546d others(12): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407253 | ||||||
chr7:130407255
|
C | CAA | 4 | a0001c0001t0002g0086a0001c0001t0026g0303a0001c0001t0034g0272others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2548_278-2547i others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407255 | ||||||
chr7:130407257
|
C | A | 6 | a0001c0001t0002g0176a0001c0001t0008g0307a0001c0001t0010g0128others(3): Show | 6 | HG00639.hp1 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-2549G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407257 | ||||||
chr7:130407259
|
C | A | 42 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(39): Show | 50 | HG01070.hp2 HG01099.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.278-2551G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407259 | ||||||
chr7:130407261
|
C | A | 4 | a0001c0001t0004g0198a0001c0001t0023g0084a0001c0001t0023g0085others(1): Show | 4 | HG00738.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2553G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407261 | ||||||
chr7:130407263
|
C | A | 1 | a0001c0001t0023g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.278-2555G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407263 | ||||||
chr7:130407567
|
T | C | 56 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(53): Show | 64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.278-2859A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407567 | ||||||
chr7:130407825
|
C | T | 70 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(67): Show | 79 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.278-3117G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407825 | ||||||
chr7:130407991
|
A | T | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.277+3131T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130407991 | ||||||
chr7:130408097
|
T | G | 4 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0066g0290others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+3025A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408097 | ||||||
chr7:130408134
|
G | A | 3 | a0001c0001t0002g0094a0001c0001t0008g0273a0001c0001t0034g0272 | 3 | HG01070.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.277+2988C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408134 | ||||||
chr7:130408211
|
C | A | 1 | a0001c0001t0058g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.277+2911G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408211 | ||||||
chr7:130408309
|
A | G | 1 | a0001c0001t0013g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.277+2813T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408309 | ||||||
chr7:130408322
|
T | A | 20 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(17): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.277+2800A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408322 | ||||||
chr7:130408349
|
G | A | 1 | a0001c0001t0044g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.277+2773C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408349 | ||||||
chr7:130408387
|
A | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+2735T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408387 | ||||||
chr7:130408806
|
G | GA | 7 | a0001c0001t0009g0013a0001c0001t0009g0107a0001c0001t0009g0108others(4): Show | 8 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+2315dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408806 | ||||||
chr7:130408943
|
G | A | 1 | a0001c0001t0013g0028 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.277+2179C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130408943 | ||||||
chr7:130409009
|
T | C | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277+2113A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409009 | ||||||
chr7:130409236
|
G | A | 1 | a0001c0001t0017g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.277+1886C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409236 | ||||||
chr7:130409237
|
C | A | 1 | a0001c0001t0017g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.277+1885G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409237 | ||||||
chr7:130409608
|
T | G | 1 | a0001c0001t0006g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.277+1514A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409608 | ||||||
chr7:130409765
|
T | C | 2 | a0001c0001t0003g0079a0001c0001t0012g0076 | 2 | NA18950.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.277+1357A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409765 | ||||||
chr7:130409930
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.277+1192G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409930 | ||||||
chr7:130409979
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.277+1143G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130409979 | ||||||
chr7:130410024
|
G | GTCTTCTT others(8): Show |
1 | a0001c0001t0004g0204 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.277+1083_277+1097d others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410024 | ||||||
chr7:130410026
|
C | CTTCTTTT others(6): Show |
5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+1083_277+1095d others(15): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410026 | ||||||
chr7:130410026
|
C | CTTCTTTT others(7): Show |
3 | a0001c0001t0023g0085a0001c0001t0027g0276a0001c0001t0087g0295 | 3 | HG02896.hp1 NA18962.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.277+1082_277+1095d others(16): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410026 | ||||||
chr7:130410026
|
C | CTTCTTTT others(8): Show |
165 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(162): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.277+1081_277+1095d others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410026 | ||||||
chr7:130410029
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0037g0300a0001c0001t0037g0301a0001c0001t0048g0027 | 3 | HG02717.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.277+1092_277+1093i others(18): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410029 | ||||||
chr7:130410029
|
C | CTTTTTTT others(10): Show |
1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277+1092_277+1093i others(19): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410029 | ||||||
chr7:130410030
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0071g0298 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.277+1091_277+1092i others(16): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410030 | ||||||
chr7:130410041
|
T | G | 1 | a0001c0001t0014g0285 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.277+1081A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410041 | ||||||
chr7:130410048
|
C | T | 11 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0038others(8): Show | 13 | HG01261.hp2 HG01975.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.277+1074G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410048 | ||||||
chr7:130410060
|
G | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0034a0001c0001t0002g0043others(3): Show | 7 | HG02015.hp2 HG02074.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+1062C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410060 | ||||||
chr7:130410087
|
G | A | 1 | a0001c0001t0008g0306 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.277+1035C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410087 | ||||||
chr7:130410129
|
A | G | 179 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(176): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.277+993T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410129 | ||||||
chr7:130410197
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.277+925A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410197 | ||||||
chr7:130410262
|
C | T | 1 | a0001c0001t0004g0192 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.277+860G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410262 | ||||||
chr7:130410274
|
G | A | 1 | a0001c0001t0042g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.277+848C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410274 | ||||||
chr7:130410279
|
G | T | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277+843C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410279 | ||||||
chr7:130410331
|
G | A | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277+791C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410331 | ||||||
chr7:130410526
|
T | C | 108 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(105): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.277+596A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410526 | ||||||
chr7:130410692
|
C | T | 6 | a0001c0001t0011g0131a0001c0001t0011g0134a0001c0001t0011g0137others(3): Show | 6 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+430G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410692 | ||||||
chr7:130410720
|
T | A | 1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277+402A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 5/10 | chr7 | 130410720 | ||||||
chr7:130411196
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG03669.hp1 | splice_region_variant&intron_variant | LOW | c.208-5A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411196 | ||||||
chr7:130411229
|
T | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.208-38A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411229 | ||||||
chr7:130411364
|
A | G | 4 | a0001c0001t0003g0129a0001c0001t0037g0300a0001c0001t0037g0301others(1): Show | 4 | HG00099.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-173T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411364 | ||||||
chr7:130411383
|
T | C | 2 | a0001c0001t0006g0104a0001c0001t0006g0118 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.208-192A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411383 | ||||||
chr7:130411480
|
T | G | 1 | a0001c0001t0026g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-289A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411480 | ||||||
chr7:130411568
|
C | T | 4 | a0001c0001t0023g0084a0001c0001t0023g0085a0001c0001t0023g0179others(1): Show | 4 | HG02615.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-377G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411568 | ||||||
chr7:130411601
|
C | T | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-410G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411601 | ||||||
chr7:130411640
|
T | C | 54 | a0001c0001t0003g0129a0001c0001t0005g0130a0001c0001t0006g0012others(51): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.208-449A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411640 | ||||||
chr7:130411781
|
C | T | 5 | a0001c0001t0003g0063a0001c0001t0003g0065a0001c0001t0003g0069others(2): Show | 5 | HG01167.hp2 HG02129.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+398G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130411781 | ||||||
chr7:130412053
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.207+126C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 4/10 | chr7 | 130412053 | ||||||
chr7:130412394
|
A | T | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-154T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412394 | ||||||
chr7:130412395
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-155C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412395 | ||||||
chr7:130412396
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-156C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412396 | ||||||
chr7:130412397
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-157A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412397 | ||||||
chr7:130412398
|
A | C | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-158T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412398 | ||||||
chr7:130412399
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-159C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412399 | ||||||
chr7:130412404
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-164T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412404 | ||||||
chr7:130412405
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-165A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412405 | ||||||
chr7:130412406
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-166G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412406 | ||||||
chr7:130412407
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-167T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412407 | ||||||
chr7:130412409
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146-169G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412409 | ||||||
chr7:130412420
|
G | T | 1 | a0001c0001t0008g0306 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.146-180C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412420 | ||||||
chr7:130412448
|
T | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-208A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412448 | ||||||
chr7:130412546
|
G | A | 1 | a0001c0001t0019g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146-306C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412546 | ||||||
chr7:130412563
|
C | T | 71 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(68): Show | 80 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.146-323G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130412563 | ||||||
chr7:130413060
|
C | T | 1 | a0001c0001t0046g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146-820G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413060 | ||||||
chr7:130413155
|
C | T | 3 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0068g0292 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.146-915G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413155 | ||||||
chr7:130413270
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.146-1030G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413270 | ||||||
chr7:130413282
|
C | T | 50 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.146-1042G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413282 | ||||||
chr7:130413367
|
T | C | 181 | a0001c0001t0001g0242a0001c0001t0001g0262a0001c0001t0002g0004others(178): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.146-1127A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413367 | ||||||
chr7:130413380
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.146-1140A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413380 | ||||||
chr7:130413584
|
A | C | 12 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(9): Show | 13 | HG00558.hp2 HG01257.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.146-1344T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413584 | ||||||
chr7:130413590
|
C | A | 2 | a0001c0001t0002g0039a0001c0001t0072g0243 | 2 | HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.146-1350G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413590 | ||||||
chr7:130413590
|
C | CA | 174 | a0001c0001t0001g0242a0001c0001t0001g0262a0001c0001t0002g0004others(171): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.146-1351dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413590 | ||||||
chr7:130413814
|
A | G | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-1574T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413814 | ||||||
chr7:130413859
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.146-1619G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130413859 | ||||||
chr7:130414227
|
A | G | 6 | a0001c0001t0014g0228a0001c0001t0014g0233a0001c0001t0014g0285others(3): Show | 6 | NA18950.hp2 NA18987.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1987T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414227 | ||||||
chr7:130414298
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.146-2058G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414298 | ||||||
chr7:130414483
|
T | C | 1 | a0001c0001t0019g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.146-2243A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414483 | ||||||
chr7:130414611
|
T | C | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.145+2308A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414611 | ||||||
chr7:130414706
|
G | A | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.145+2213C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414706 | ||||||
chr7:130414802
|
G | A | 1 | a0001c0001t0025g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.145+2117C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414802 | ||||||
chr7:130414844
|
G | A | 1 | a0001c0001t0010g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.145+2075C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130414844 | ||||||
chr7:130415271
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0231a0001c0001t0001g0267others(2): Show | 11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.145+1648A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415271 | ||||||
chr7:130415443
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+1476C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415443 | ||||||
chr7:130415589
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.145+1330G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415589 | ||||||
chr7:130415637
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+1282C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415637 | ||||||
chr7:130415678
|
G | T | 54 | a0001c0001t0003g0129a0001c0001t0005g0130a0001c0001t0006g0012others(51): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.145+1241C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415678 | ||||||
chr7:130415848
|
A | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+1071T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415848 | ||||||
chr7:130415875
|
T | C | 1 | a0001c0001t0011g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.145+1044A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415875 | ||||||
chr7:130415883
|
G | A | 1 | a0001c0001t0073g0289 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.145+1036C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415883 | ||||||
chr7:130415889
|
G | A | 1 | a0001c0001t0024g0011 | 2 | HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.145+1030C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415889 | ||||||
chr7:130415922
|
T | C | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.145+997A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130415922 | ||||||
chr7:130416041
|
A | C | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145+878T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416041 | ||||||
chr7:130416245
|
C | A | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.145+674G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416245 | ||||||
chr7:130416468
|
C | T | 4 | a0001c0001t0003g0129a0001c0001t0037g0300a0001c0001t0037g0301others(1): Show | 4 | HG00099.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+451G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416468 | ||||||
chr7:130416481
|
C | T | 1 | a0001c0001t0009g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.145+438G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416481 | ||||||
chr7:130416520
|
AG | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+398delC | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416520 | ||||||
chr7:130416532
|
A | G | 56 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(53): Show | 64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.145+387T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416532 | ||||||
chr7:130416547
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+372G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416547 | ||||||
chr7:130416561
|
T | C | 4 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0066g0290others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+358A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416561 | ||||||
chr7:130416593
|
T | C | 1 | a0001c0001t0005g0148 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.145+326A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416593 | ||||||
chr7:130416608
|
T | G | 5 | a0001c0001t0050g0022a0001c0001t0054g0023a0001c0001t0055g0024others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+311A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416608 | ||||||
chr7:130416623
|
A | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+296T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416623 | ||||||
chr7:130416642
|
G | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+277C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416642 | ||||||
chr7:130416861
|
C | G | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.145+58G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 3/10 | chr7 | 130416861 | ||||||
chr7:130417036
|
A | G | 1 | a0001c0001t0044g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98-70T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417036 | ||||||
chr7:130417263
|
A | G | 1 | a0001c0001t0016g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.98-297T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417263 | ||||||
chr7:130417320
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-354C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417320 | ||||||
chr7:130417378
|
G | A | 1 | a0001c0001t0035g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.98-412C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417378 | ||||||
chr7:130417414
|
G | A | 1 | a0001c0001t0066g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.98-448C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417414 | ||||||
chr7:130417862
|
C | G | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-896G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130417862 | ||||||
chr7:130418110
|
T | G | 3 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0068g0292 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.98-1144A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418110 | ||||||
chr7:130418259
|
T | C | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.98-1293A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418259 | ||||||
chr7:130418333
|
C | CTCTG | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-1368_98-1367ins others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418333 | ||||||
chr7:130418334
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-1368C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418334 | ||||||
chr7:130418347
|
A | G | 1 | a0002c0002t0005g0074 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.98-1381T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418347 | ||||||
chr7:130418405
|
A | G | 50 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.98-1439T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418405 | ||||||
chr7:130418550
|
T | A | 1 | a0001c0001t0045g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98-1584A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418550 | ||||||
chr7:130418658
|
C | G | 56 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(53): Show | 64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.98-1692G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130418658 | ||||||
chr7:130419254
|
T | C | 1 | a0001c0001t0004g0203 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.98-2288A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419254 | ||||||
chr7:130419446
|
T | C | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-2480A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419446 | ||||||
chr7:130419467
|
GA | G | 4 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0066g0290others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2502delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419467 | ||||||
chr7:130419472
|
C | T | 1 | a0001c0001t0045g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98-2506G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419472 | ||||||
chr7:130419501
|
T | C | 1 | a0001c0001t0019g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-2535A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419501 | ||||||
chr7:130419535
|
T | G | 56 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(53): Show | 64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.98-2569A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419535 | ||||||
chr7:130419581
|
T | A | 93 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0036others(90): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.98-2615A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419581 | ||||||
chr7:130419581
|
T | TA | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-2616dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419581 | ||||||
chr7:130419582
|
A | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0262a0001c0001t0007g0261others(1): Show | 4 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2616T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419582 | ||||||
chr7:130419670
|
C | T | 9 | a0001c0001t0003g0021a0001c0001t0003g0068a0001c0001t0003g0082others(6): Show | 10 | HG01891.hp1 HG01943.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.98-2704G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419670 | ||||||
chr7:130419950
|
T | TAC | 34 | a0001c0001t0001g0240a0001c0001t0004g0195a0001c0001t0004g0203others(31): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.98-2986_98-2985dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130419950 | ||||||
chr7:130420124
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3158G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420124 | ||||||
chr7:130420215
|
A | G | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.98-3249T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420215 | ||||||
chr7:130420240
|
G | A | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-3274C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420240 | ||||||
chr7:130420328
|
C | CA | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(72): Show | 91 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.98-3363dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | ||||||
chr7:130420328
|
C | CAA | 57 | a0001c0001t0001g0219a0001c0001t0001g0254a0001c0001t0001g0259others(54): Show | 65 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.98-3364_98-3363dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | ||||||
chr7:130420328
|
CA | C | 96 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0036others(93): Show | 102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.98-3363delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | ||||||
chr7:130420328
|
CAA | C | 7 | a0001c0001t0005g0130a0001c0001t0022g0172a0001c0001t0030g0132others(4): Show | 7 | HG02056.hp2 HG02080.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-3364_98-3363del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | ||||||
chr7:130420328
|
CAAA | C | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-3365_98-3363del others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420328 | ||||||
chr7:130420410
|
G | A | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.98-3444C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420410 | ||||||
chr7:130420412
|
A | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3446T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420412 | ||||||
chr7:130420539
|
C | T | 5 | a0001c0001t0011g0131a0001c0001t0011g0134a0001c0001t0030g0132others(2): Show | 5 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-3573G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420539 | ||||||
chr7:130420600
|
C | T | 2 | a0001c0001t0019g0157a0001c0001t0019g0163 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.98-3634G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420600 | ||||||
chr7:130420643
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3677C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420643 | ||||||
chr7:130420687
|
G | A | 1 | a0001c0001t0030g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.98-3721C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420687 | ||||||
chr7:130420728
|
C | T | 1 | a0001c0001t0009g0107 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.98-3762G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420728 | ||||||
chr7:130420759
|
G | A | 5 | a0001c0001t0050g0022a0001c0001t0054g0023a0001c0001t0055g0024others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-3793C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420759 | ||||||
chr7:130420782
|
T | A | 45 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(42): Show | 49 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-3816A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420782 | ||||||
chr7:130420843
|
A | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3877T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420843 | ||||||
chr7:130420931
|
A | C | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-3965T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420931 | ||||||
chr7:130420965
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.98-3999C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130420965 | ||||||
chr7:130421257
|
G | C | 9 | a0001c0001t0006g0012a0001c0001t0006g0101a0001c0001t0006g0102others(6): Show | 10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-4291C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421257 | ||||||
chr7:130421737
|
G | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-4771C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421737 | ||||||
chr7:130421904
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.98-4938G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421904 | ||||||
chr7:130421991
|
A | G | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-5025T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130421991 | ||||||
chr7:130422026
|
A | G | 1 | a0001c0001t0003g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.98-5060T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422026 | ||||||
chr7:130422237
|
T | C | 2 | a0001c0001t0008g0213a0001c0001t0021g0210 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.98-5271A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422237 | ||||||
chr7:130422548
|
C | T | 101 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(98): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.97+5407G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422548 | ||||||
chr7:130422684
|
C | T | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.97+5271G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130422684 | ||||||
chr7:130423037
|
C | T | 1 | a0001c0001t0008g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.97+4918G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423037 | ||||||
chr7:130423239
|
C | T | 1 | a0001c0001t0008g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97+4716G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423239 | ||||||
chr7:130423348
|
A | G | 177 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.97+4607T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423348 | ||||||
chr7:130423592
|
T | C | 1 | a0001c0001t0063g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.97+4363A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423592 | ||||||
chr7:130423882
|
T | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+4073A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423882 | ||||||
chr7:130423967
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0262a0001c0001t0007g0261others(1): Show | 4 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3988T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130423967 | ||||||
chr7:130424029
|
G | A | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+3926C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424029 | ||||||
chr7:130424194
|
C | T | 3 | a0001c0001t0003g0063a0001c0001t0003g0065a0001c0001t0003g0071 | 3 | HG01167.hp2 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.97+3761G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424194 | ||||||
chr7:130424399
|
CA | C | 20 | a0001c0001t0001g0231a0001c0001t0001g0237a0001c0001t0001g0240others(17): Show | 21 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.97+3555delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424399 | ||||||
chr7:130424597
|
T | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+3358A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424597 | ||||||
chr7:130424646
|
T | C | 54 | a0001c0001t0003g0129a0001c0001t0005g0130a0001c0001t0006g0012others(51): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.97+3309A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424646 | ||||||
chr7:130424698
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+3257G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130424698 | ||||||
chr7:130425155
|
G | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0118 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.97+2800C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425155 | ||||||
chr7:130425217
|
A | G | 11 | a0001c0001t0002g0004a0001c0001t0002g0037a0001c0001t0002g0038others(8): Show | 13 | HG01261.hp2 HG01975.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+2738T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425217 | ||||||
chr7:130425238
|
A | AC | 197 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(194): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.97+2716dupG | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425238 | ||||||
chr7:130425263
|
A | C | 62 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(59): Show | 70 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.97+2692T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425263 | ||||||
chr7:130425474
|
T | C | 1 | a0001c0001t0016g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.97+2481A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425474 | ||||||
chr7:130425501
|
C | A | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+2454G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425501 | ||||||
chr7:130425513
|
A | G | 22 | a0001c0001t0003g0140a0001c0001t0005g0016a0001c0001t0005g0141others(19): Show | 24 | HG01175.hp1 HG02004.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+2442T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425513 | ||||||
chr7:130425588
|
T | C | 177 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.97+2367A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425588 | ||||||
chr7:130425638
|
T | C | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+2317A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425638 | ||||||
chr7:130425648
|
G | C | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.97+2307C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425648 | ||||||
chr7:130425699
|
A | C | 15 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(12): Show | 16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+2256T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425699 | ||||||
chr7:130425857
|
A | G | 2 | a0001c0001t0004g0190a0001c0001t0018g0188 | 2 | HG01361.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.97+2098T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425857 | ||||||
chr7:130425890
|
A | G | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+2065T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130425890 | ||||||
chr7:130426186
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1769G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426186 | ||||||
chr7:130426317
|
A | G | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+1638T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426317 | ||||||
chr7:130426367
|
G | A | 1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+1588C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426367 | ||||||
chr7:130426437
|
GGAAA | G | 9 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(6): Show | 10 | HG00558.hp2 HG01934.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+1514_97+1517del others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426437 | ||||||
chr7:130426438
|
GAAAGA | G | 62 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(59): Show | 70 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.97+1512_97+1516del others(5): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426438 | ||||||
chr7:130426445
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+1510T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426445 | ||||||
chr7:130426449
|
A | ATCAGTAA others(10): Show |
1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+1505_97+1506ins others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426449 | ||||||
chr7:130426452
|
A | C | 1 | a0001c0001t0005g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.97+1503T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426452 | ||||||
chr7:130426484
|
A | G | 1 | a0001c0001t0006g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+1471T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426484 | ||||||
chr7:130426556
|
C | T | 1 | a0001c0001t0045g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.97+1399G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426556 | ||||||
chr7:130426558
|
T | A | 1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+1397A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426558 | ||||||
chr7:130426979
|
CG | C | 64 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(61): Show | 72 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.97+975delC | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130426979 | ||||||
chr7:130427085
|
G | A | 1 | a0001c0001t0004g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.97+870C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427085 | ||||||
chr7:130427099
|
G | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+856C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427099 | ||||||
chr7:130427241
|
C | T | 64 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(61): Show | 72 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.97+714G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427241 | ||||||
chr7:130427281
|
A | C | 3 | a0001c0001t0022g0170a0001c0001t0022g0171a0001c0001t0022g0172 | 3 | HG01884.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.97+674T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427281 | ||||||
chr7:130427291
|
A | C | 4 | a0001c0001t0003g0140a0001c0001t0005g0153a0001c0001t0005g0159others(1): Show | 4 | NA18964.hp2 NA19060.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+664T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427291 | ||||||
chr7:130427374
|
G | A | 1 | a0001c0001t0007g0256 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.97+581C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427374 | ||||||
chr7:130427459
|
T | C | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+496A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427459 | ||||||
chr7:130427469
|
T | C | 1 | a0001c0001t0011g0180 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.97+486A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427469 | ||||||
chr7:130427477
|
C | A | 1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+478G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427477 | ||||||
chr7:130427478
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+477A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427478 | ||||||
chr7:130427481
|
A | T | 1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.97+474T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427481 | ||||||
chr7:130427525
|
T | C | 3 | a0001c0001t0022g0170a0001c0001t0022g0171a0001c0001t0022g0172 | 3 | HG01884.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.97+430A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427525 | ||||||
chr7:130427532
|
T | C | 2 | a0001c0001t0003g0064a0001c0001t0003g0078 | 2 | HG02895.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97+423A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427532 | ||||||
chr7:130427827
|
C | T | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.97+128G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427827 | ||||||
chr7:130427878
|
C | T | 1 | a0001c0001t0007g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.97+77G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427878 | ||||||
chr7:130427912
|
C | T | 1 | a0001c0001t0016g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97+43G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 2/10 | chr7 | 130427912 | ||||||
chr7:130428062
|
A | T | 1 | a0001c0001t0043g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.34-44T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428062 | ||||||
chr7:130428162
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.34-144C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428162 | ||||||
chr7:130428163
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-145G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428163 | ||||||
chr7:130428331
|
G | A | 4 | a0001c0001t0029g0166a0001c0001t0029g0167a0001c0001t0064g0274others(1): Show | 4 | HG01257.hp1 HG03516.hp2 NA21309.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-313C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428331 | ||||||
chr7:130428425
|
A | T | 1 | a0001c0001t0002g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.34-407T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428425 | ||||||
chr7:130428428
|
C | CA | 103 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0004others(100): Show | 115 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.34-411dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | ||||||
chr7:130428428
|
C | CAA | 52 | a0001c0001t0002g0086a0001c0001t0002g0176a0001c0001t0003g0129others(49): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.34-412_34-411dupTT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | ||||||
chr7:130428428
|
C | CAAA | 12 | a0001c0001t0006g0105a0001c0001t0006g0118a0001c0001t0011g0115others(9): Show | 12 | HG01192.hp2 HG01361.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.34-413_34-411dupTT others(1): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | ||||||
chr7:130428428
|
CA | C | 15 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0003g0140others(12): Show | 16 | HG02074.hp2 NA18944.hp2 NA18964.hp1 others(13): Show |
intron_variant | MODIFIER | c.34-411delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | ||||||
chr7:130428428
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34-421_34-411delTT others(9): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428428 | ||||||
chr7:130428688
|
T | C | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-670A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428688 | ||||||
chr7:130428696
|
AAGGTCAG others(1): Show |
A | 2 | a0001c0001t0004g0018a0001c0001t0004g0205 | 3 | HG03490.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.34-686_34-679delCC others(6): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428696 | ||||||
chr7:130428718
|
T | C | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-700A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428718 | ||||||
chr7:130428792
|
C | T | 1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34-774G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428792 | ||||||
chr7:130428857
|
G | A | 1 | a0001c0001t0008g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.34-839C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428857 | ||||||
chr7:130428914
|
A | AAAAT | 12 | a0001c0001t0002g0045a0001c0001t0003g0140a0001c0001t0005g0153others(9): Show | 12 | HG00621.hp2 HG01175.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.34-900_34-897dupAT others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428914 | ||||||
chr7:130428917
|
AT | A | 3 | a0001c0001t0064g0274a0001c0001t0065g0286a0001c0001t0066g0290 | 3 | HG01257.hp1 HG03098.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-900delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428917 | ||||||
chr7:130428918
|
T | A | 64 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(61): Show | 73 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.34-900A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428918 | ||||||
chr7:130428922
|
T | A | 9 | a0001c0001t0004g0185a0001c0001t0004g0198a0001c0001t0023g0179others(6): Show | 9 | HG00738.hp2 HG01257.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.34-904A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428922 | ||||||
chr7:130428925
|
A | AAT | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-908_34-907insAT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428925 | ||||||
chr7:130428926
|
T | A | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-908A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428926 | ||||||
chr7:130428960
|
G | T | 2 | a0001c0001t0003g0073a0001c0001t0007g0232 | 2 | NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.34-942C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130428960 | ||||||
chr7:130429034
|
A | G | 1 | a0001c0001t0066g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34-1016T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429034 | ||||||
chr7:130429051
|
G | T | 29 | a0001c0001t0005g0130a0001c0001t0009g0013a0001c0001t0009g0088others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.34-1033C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429051 | ||||||
chr7:130429329
|
CAT | C | 7 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0173others(4): Show | 7 | HG01099.hp1 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-1313_34-1312del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429329 | ||||||
chr7:130429471
|
T | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0071 | 2 | HG01167.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.34-1453A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429471 | ||||||
chr7:130429508
|
T | G | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-1490A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429508 | ||||||
chr7:130429527
|
A | G | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-1509T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429527 | ||||||
chr7:130429540
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-1522C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429540 | ||||||
chr7:130429569
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.34-1551G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429569 | ||||||
chr7:130429624
|
T | C | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.34-1606A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429624 | ||||||
chr7:130429654
|
T | C | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.34-1636A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429654 | ||||||
chr7:130429724
|
C | T | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.34-1706G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429724 | ||||||
chr7:130429983
|
C | T | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.34-1965G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429983 | ||||||
chr7:130429984
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.34-1966C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130429984 | ||||||
chr7:130430054
|
A | T | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-2036T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430054 | ||||||
chr7:130430401
|
C | T | 2 | a0001c0001t0005g0148a0001c0001t0031g0149 | 2 | HG01884.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.34-2383G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430401 | ||||||
chr7:130430412
|
TTG | T | 62 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(59): Show | 70 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.34-2396_34-2395del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430412 | ||||||
chr7:130430427
|
C | A | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.34-2409G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430427 | ||||||
chr7:130430508
|
T | C | 54 | a0001c0001t0003g0129a0001c0001t0005g0130a0001c0001t0006g0012others(51): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.34-2490A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430508 | ||||||
chr7:130430700
|
C | T | 1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34-2682G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430700 | ||||||
chr7:130430729
|
C | T | 2 | a0001c0001t0048g0027a0004c0003t0067g0309 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.34-2711G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430729 | ||||||
chr7:130430768
|
G | A | 60 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(57): Show | 68 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.34-2750C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430768 | ||||||
chr7:130430872
|
G | C | 1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34-2854C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430872 | ||||||
chr7:130430995
|
G | A | 1 | a0001c0001t0012g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.34-2977C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130430995 | ||||||
chr7:130431125
|
T | TAAAA | 62 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(59): Show | 70 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.34-3111_34-3108dup others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431125 | ||||||
chr7:130431183
|
CT | C | 176 | a0001c0001t0001g0259a0001c0001t0002g0004a0001c0001t0002g0009others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.34-3166delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431183 | ||||||
chr7:130431192
|
T | A | 1 | a0001c0001t0003g0079 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.34-3174A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431192 | ||||||
chr7:130431369
|
T | C | 1 | a0001c0001t0043g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.34-3351A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431369 | ||||||
chr7:130431391
|
T | C | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.34-3373A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431391 | ||||||
chr7:130431493
|
G | A | 56 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(53): Show | 64 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.34-3475C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431493 | ||||||
chr7:130431681
|
A | G | 68 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(65): Show | 77 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.34-3663T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431681 | ||||||
chr7:130431738
|
A | G | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-3720T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431738 | ||||||
chr7:130431756
|
G | A | 15 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(12): Show | 16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.34-3738C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431756 | ||||||
chr7:130431780
|
G | A | 6 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 7 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-3762C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431780 | ||||||
chr7:130431962
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.34-3944A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431962 | ||||||
chr7:130431996
|
C | G | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-3978G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130431996 | ||||||
chr7:130432063
|
C | G | 1 | a0001c0001t0005g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.34-4045G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432063 | ||||||
chr7:130432069
|
T | C | 1 | a0001c0001t0066g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34-4051A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432069 | ||||||
chr7:130432171
|
AT | A | 68 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(65): Show | 77 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.34-4154delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432171 | ||||||
chr7:130432390
|
G | C | 1 | a0001c0001t0006g0177 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.34-4372C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432390 | ||||||
chr7:130432423
|
G | A | 5 | a0001c0001t0050g0022a0001c0001t0054g0023a0001c0001t0055g0024others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.34-4405C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432423 | ||||||
chr7:130432554
|
C | T | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-4536G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432554 | ||||||
chr7:130432588
|
C | CA | 51 | a0001c0001t0001g0260a0001c0001t0001g0262a0001c0001t0001g0263others(48): Show | 52 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.34-4571dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432588
|
C | CAA | 8 | a0001c0001t0002g0139a0001c0001t0005g0159a0001c0001t0013g0007others(5): Show | 9 | HG01891.hp2 HG01934.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.34-4572_34-4571dup others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432588
|
C | CAAA | 8 | a0001c0001t0013g0028a0001c0001t0027g0275a0001c0001t0036g0293others(5): Show | 8 | HG00558.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-4573_34-4571dup others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432588
|
C | CAAAA | 40 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0173others(37): Show | 45 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.34-4574_34-4571dup others(4): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432588
|
C | CAAAAA | 14 | a0001c0001t0002g0086a0001c0001t0002g0097a0001c0001t0002g0175others(11): Show | 17 | HG01106.hp1 HG01123.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.34-4575_34-4571dup others(5): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432588
|
CA | C | 10 | a0001c0001t0003g0021a0001c0001t0009g0119a0001c0001t0014g0228others(7): Show | 10 | HG02630.hp1 HG02922.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.34-4571delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432588
|
CAAAAAAA | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG00408.hp2 HG02015.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-4577_34-4571del others(7): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432588 | ||||||
chr7:130432656
|
G | C | 1 | a0001c0001t0045g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.34-4638C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432656 | ||||||
chr7:130432657
|
A | G | 70 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(67): Show | 79 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.34-4639T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432657 | ||||||
chr7:130432777
|
C | T | 1 | a0001c0001t0011g0087 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.34-4759G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432777 | ||||||
chr7:130432937
|
A | C | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-4919T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432937 | ||||||
chr7:130432961
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-4943C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130432961 | ||||||
chr7:130433064
|
G | C | 1 | a0001c0001t0046g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.34-5046C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433064 | ||||||
chr7:130433082
|
G | A | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-5064C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433082 | ||||||
chr7:130433254
|
A | G | 15 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(12): Show | 16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.34-5236T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433254 | ||||||
chr7:130433960
|
G | A | 2 | a0001c0001t0064g0274a0001c0001t0065g0286 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.34-5942C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130433960 | ||||||
chr7:130434000
|
T | G | 1 | a0001c0001t0041g0144 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.34-5982A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434000 | ||||||
chr7:130434217
|
A | G | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.34-6199T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434217 | ||||||
chr7:130434258
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-6240G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434258 | ||||||
chr7:130434259
|
C | T | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-6241G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434259 | ||||||
chr7:130434293
|
T | C | 25 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(22): Show | 27 | HG00558.hp2 HG01167.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.34-6275A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434293 | ||||||
chr7:130434356
|
T | A | 65 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(62): Show | 73 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.34-6338A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434356 | ||||||
chr7:130434357
|
A | T | 6 | a0001c0001t0009g0106a0001c0001t0013g0007a0001c0001t0013g0028others(3): Show | 7 | HG00558.hp2 HG01255.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-6339T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434357 | ||||||
chr7:130434372
|
T | G | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34-6354A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434372 | ||||||
chr7:130434389
|
G | T | 172 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(169): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.34-6371C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434389 | ||||||
chr7:130434403
|
G | C | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.34-6385C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434403 | ||||||
chr7:130434501
|
A | G | 4 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0066g0290others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+6433T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130434501 | ||||||
chr7:130435156
|
C | A | 1 | a0001c0001t0008g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.33+5778G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435156 | ||||||
chr7:130435442
|
G | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0101a0001c0001t0006g0102others(6): Show | 10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+5492C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435442 | ||||||
chr7:130435482
|
C | T | 3 | a0001c0001t0003g0147a0001c0001t0012g0146a0001c0001t0025g0281 | 3 | HG01261.hp1 HG01496.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.33+5452G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435482 | ||||||
chr7:130435529
|
C | T | 50 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.33+5405G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435529 | ||||||
chr7:130435667
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.33+5267C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435667 | ||||||
chr7:130435680
|
G | A | 1 | a0001c0001t0004g0203 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.33+5254C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435680 | ||||||
chr7:130435737
|
C | T | 1 | a0004c0003t0067g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33+5197G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435737 | ||||||
chr7:130435771
|
A | G | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+5163T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435771 | ||||||
chr7:130435893
|
G | A | 1 | a0001c0001t0015g0061 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.33+5041C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130435893 | ||||||
chr7:130436041
|
C | T | 1 | a0001c0001t0019g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33+4893G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436041 | ||||||
chr7:130436062
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33+4872C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436062 | ||||||
chr7:130436082
|
C | T | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+4852G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436082 | ||||||
chr7:130436113
|
C | T | 1 | a0001c0001t0041g0144 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.33+4821G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436113 | ||||||
chr7:130436191
|
C | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0101a0001c0001t0006g0102others(6): Show | 10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+4743G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436191 | ||||||
chr7:130436266
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.33+4668G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436266 | ||||||
chr7:130436285
|
GA | G | 15 | a0001c0001t0003g0021a0001c0001t0003g0063a0001c0001t0003g0065others(12): Show | 16 | HG01167.hp2 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.33+4648delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436285 | ||||||
chr7:130436304
|
C | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+4630G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436304 | ||||||
chr7:130436342
|
A | T | 177 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.33+4592T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436342 | ||||||
chr7:130436407
|
T | C | 1 | a0001c0001t0089g0310 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.33+4527A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436407 | ||||||
chr7:130436578
|
TGTACTCA others(19): Show |
T | 50 | a0001c0001t0005g0130a0001c0001t0006g0012a0001c0001t0006g0101others(47): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.33+4330_33+4355del others(26): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436578 | ||||||
chr7:130436605
|
G | A | 50 | a0001c0001t0005g0130a0001c0001t0006g0012a0001c0001t0006g0101others(47): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.33+4329C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436605 | ||||||
chr7:130436641
|
CTA | C | 10 | a0001c0001t0002g0176a0001c0001t0004g0018a0001c0001t0004g0205others(7): Show | 11 | HG01257.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.33+4291_33+4292del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436641 | ||||||
chr7:130436642
|
TA | T | 54 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(51): Show | 61 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.33+4291delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436642 | ||||||
chr7:130436643
|
A | T | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+4291T>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436643 | ||||||
chr7:130436643
|
AT | A | 53 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(50): Show | 57 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.33+4290delA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436643 | ||||||
chr7:130436643
|
ATT | A | 57 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(54): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.33+4289_33+4290del others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436643 | ||||||
chr7:130436655
|
T | C | 1 | a0001c0001t0013g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.33+4279A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436655 | ||||||
chr7:130436762
|
A | G | 66 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(63): Show | 74 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.33+4172T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436762 | ||||||
chr7:130436765
|
G | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(104): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.33+4169C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436765 | ||||||
chr7:130436821
|
G | T | 2 | a0001c0001t0005g0142a0001c0001t0005g0160 | 2 | NA19011.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.33+4113C>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436821 | ||||||
chr7:130436844
|
C | G | 1 | a0001c0001t0087g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33+4090G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436844 | ||||||
chr7:130436940
|
G | A | 50 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 54 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.33+3994C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130436940 | ||||||
chr7:130437012
|
C | G | 66 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(63): Show | 74 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.33+3922G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437012 | ||||||
chr7:130437055
|
C | A | 66 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(63): Show | 74 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.33+3879G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437055 | ||||||
chr7:130437173
|
G | A | 5 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0029others(2): Show | 6 | HG00558.hp2 HG01934.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+3761C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437173 | ||||||
chr7:130437365
|
C | CA | 171 | a0001c0001t0001g0269a0001c0001t0002g0004a0001c0001t0002g0009others(168): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.33+3568dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437365 | ||||||
chr7:130437412
|
A | G | 173 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(170): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.33+3522T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437412 | ||||||
chr7:130437581
|
G | A | 1 | a0001c0001t0005g0160 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.33+3353C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437581 | ||||||
chr7:130437595
|
A | AC | 106 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(103): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.33+3338dupG | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437595 | ||||||
chr7:130437759
|
T | A | 3 | a0001c0001t0036g0293a0001c0001t0036g0294a0001c0001t0068g0292 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.33+3175A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437759 | ||||||
chr7:130437764
|
C | CA | 9 | a0001c0001t0001g0271a0001c0001t0001g0302a0001c0001t0003g0082others(6): Show | 9 | HG00597.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.33+3169dupT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | ||||||
chr7:130437764
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0013g0007a0001c0001t0013g0028a0001c0001t0013g0168 | 4 | HG00558.hp2 NA18969.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+3153_33+3169dup others(17): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | ||||||
chr7:130437764
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0013g0029 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.33+3152_33+3169dup others(18): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | ||||||
chr7:130437764
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0013g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.33+3147_33+3169dup others(23): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | ||||||
chr7:130437764
|
CA | C | 6 | a0001c0001t0001g0219a0001c0001t0003g0063a0001c0001t0003g0064others(3): Show | 6 | HG01167.hp2 HG01934.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+3169delT | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437764 | ||||||
chr7:130437774
|
AAAAAAAA others(14): Show |
A | 1 | a0003c0004t0081g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.33+3139_33+3159del others(21): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437774 | ||||||
chr7:130437775
|
AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33+3139_33+3158del others(20): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437775 | ||||||
chr7:130437777
|
A | AAAG | 37 | a0001c0001t0004g0005a0001c0001t0004g0018a0001c0001t0004g0184others(34): Show | 45 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.33+3156_33+3157ins others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437777 | ||||||
chr7:130437777
|
A | AAG | 20 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(17): Show | 20 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.33+3156_33+3157ins others(2): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437777 | ||||||
chr7:130437784
|
AAAAAGAA others(4): Show |
A | 3 | a0001c0001t0008g0306a0001c0001t0016g0099a0001c0001t0026g0308 | 3 | HG02965.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.33+3139_33+3149del others(11): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437784 | ||||||
chr7:130437785
|
AAAAGAAA others(3): Show |
A | 38 | a0001c0001t0003g0129a0001c0001t0005g0130a0001c0001t0006g0012others(35): Show | 40 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.33+3139_33+3148del others(10): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437785 | ||||||
chr7:130437786
|
AAAGAAAA others(2): Show |
A | 44 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0036others(41): Show | 47 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.33+3139_33+3147del others(9): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437786 | ||||||
chr7:130437787
|
AAGAAAAA others(1): Show |
A | 15 | a0001c0001t0002g0010a0001c0001t0002g0051a0001c0001t0002g0052others(12): Show | 16 | HG02015.hp2 HG02074.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.33+3139_33+3146del others(8): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437787 | ||||||
chr7:130437789
|
G | A | 1 | a0001c0001t0029g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.33+3145C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437789 | ||||||
chr7:130437795
|
G | A | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+3139C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130437795 | ||||||
chr7:130438112
|
G | A | 1 | a0001c0001t0004g0204 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.33+2822C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438112 | ||||||
chr7:130438312
|
C | T | 1 | a0001c0001t0018g0188 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.33+2622G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438312 | ||||||
chr7:130438332
|
C | T | 65 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(62): Show | 73 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.33+2602G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438332 | ||||||
chr7:130438401
|
C | A | 171 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(168): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.33+2533G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438401 | ||||||
chr7:130438450
|
C | T | 176 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.33+2484G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438450 | ||||||
chr7:130438455
|
A | C | 1 | a0001c0001t0003g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.33+2479T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438455 | ||||||
chr7:130438473
|
T | C | 31 | a0001c0001t0002g0086a0001c0001t0002g0094a0001c0001t0002g0096others(28): Show | 31 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.33+2461A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438473 | ||||||
chr7:130438610
|
C | T | 1 | a0001c0001t0012g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.33+2324G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438610 | ||||||
chr7:130438771
|
A | C | 4 | a0001c0001t0020g0014a0001c0001t0020g0122a0001c0001t0020g0123others(1): Show | 5 | NA18747.hp1 NA18982.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+2163T>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438771 | ||||||
chr7:130438860
|
T | C | 1 | a0001c0001t0066g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33+2074A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438860 | ||||||
chr7:130438869
|
T | A | 5 | a0001c0001t0008g0279a0001c0001t0027g0275a0001c0001t0027g0276others(2): Show | 5 | HG00438.hp2 NA18943.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+2065A>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438869 | ||||||
chr7:130438998
|
T | C | 1 | a0001c0001t0005g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33+1936A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130438998 | ||||||
chr7:130439009
|
A | G | 1 | a0001c0001t0048g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.33+1925T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439009 | ||||||
chr7:130439023
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0008g0307 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.33+1911A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439023 | ||||||
chr7:130439078
|
C | T | 2 | a0001c0001t0066g0290a0001c0001t0087g0295 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33+1856G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439078 | ||||||
chr7:130439084
|
C | T | 1 | a0001c0001t0066g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33+1850G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439084 | ||||||
chr7:130439149
|
T | G | 2 | a0001c0001t0002g0086a0001c0001t0008g0307 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.33+1785A>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439149 | ||||||
chr7:130439171
|
C | G | 1 | a0001c0001t0066g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33+1763G>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439171 | ||||||
chr7:130439251
|
G | C | 8 | a0001c0001t0002g0086a0001c0001t0002g0173a0001c0001t0002g0174others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+1683C>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439251 | ||||||
chr7:130439298
|
G | A | 38 | a0001c0001t0002g0086a0001c0001t0002g0120a0001c0001t0006g0012others(35): Show | 40 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.33+1636C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439298 | ||||||
chr7:130439349
|
G | GT | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(252): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.33+1584dupA | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439349 | ||||||
chr7:130439468
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(205): Show | 239 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.33+1466G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439468 | ||||||
chr7:130439554
|
G | A | 1 | a0001c0001t0023g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33+1380C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439554 | ||||||
chr7:130439573
|
C | T | 4 | a0001c0001t0004g0184a0001c0001t0004g0185a0001c0001t0014g0186others(1): Show | 4 | NA18944.hp2 NA18964.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+1361G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439573 | ||||||
chr7:130439641
|
C | T | 5 | a0001c0001t0050g0022a0001c0001t0054g0023a0001c0001t0055g0024others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+1293G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439641 | ||||||
chr7:130439675
|
C | T | 1 | a0001c0001t0071g0298 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.33+1259G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439675 | ||||||
chr7:130439715
|
A | G | 5 | a0001c0001t0050g0022a0001c0001t0054g0023a0001c0001t0055g0024others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+1219T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439715 | ||||||
chr7:130439862
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.33+1072G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439862 | ||||||
chr7:130439993
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(131): Show | 155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.33+941G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130439993 | ||||||
chr7:130440006
|
C | T | 1 | a0001c0001t0025g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.33+928G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440006 | ||||||
chr7:130440050
|
G | A | 11 | a0001c0001t0001g0302a0001c0001t0004g0299a0001c0001t0008g0306others(8): Show | 11 | HG00099.hp1 HG01993.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.33+884C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440050 | ||||||
chr7:130440056
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(134): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.33+878T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440056 | ||||||
chr7:130440107
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0183others(135): Show | 159 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.33+827A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440107 | ||||||
chr7:130440136
|
C | T | 3 | a0001c0001t0001g0287a0001c0001t0073g0289a0001c0001t0076g0288 | 3 | HG02486.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+798G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440136 | ||||||
chr7:130440144
|
C | A | 1 | a0001c0001t0019g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.33+790G>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440144 | ||||||
chr7:130440188
|
T | C | 1 | a0001c0001t0053g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.33+746A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440188 | ||||||
chr7:130440314
|
G | A | 2 | a0001c0001t0029g0166a0001c0001t0029g0167 | 2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+620C>T | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440314 | ||||||
chr7:130440363
|
A | G | 1 | a0001c0001t0003g0021 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33+571T>C | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440363 | ||||||
chr7:130440699
|
T | C | 23 | a0001c0001t0001g0287a0001c0001t0001g0302a0001c0001t0004g0299others(20): Show | 23 | HG00099.hp1 HG01891.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.33+235A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440699 | ||||||
chr7:130440782
|
G | GCCCGC | 12 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0002g0175others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.33+147_33+151dupGC others(3): Show |
CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440782 | ||||||
chr7:130440793
|
C | T | 1 | a0001c0001t0033g0181 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.33+141G>A | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440793 | ||||||
chr7:130440890
|
T | C | 1 | a0001c0001t0011g0180 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.33+44A>G | CEP41 | ENSG00000106477.20 | transcript | ENST00000223208.10 | protein_coding | 1/10 | chr7 | 130440890 |