Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84131 |
|---|---|
| ensemblid | ENSG00000148019.14 |
| hgncid | 25740 |
| symbol | CEP78 |
| name | centrosomal protein 78 |
| refseq_nuc | NM_001330691.3 |
| refseq_prot | NP_001317620.1 |
| ensembl_nuc | ENST00000643273.2 |
| ensembl_prot | ENSP00000496423.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 78236075 |
| end | 78279690 |
| strand | + |
| ver | v1.2 |
| region | chr9:78236075-78279690 |
| region5000 | chr9:78231075-78284690 |
| regionname0 | CEP78_chr9_78236075_78279690 |
| regionname5000 | CEP78_chr9_78231075_78284690 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 705 | 335 | 84 | 72 | 127 | 14 | 36 | 91 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0002 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0003 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0004 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0005 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0006 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2118 | 205 | 43 | 45 | 82 | 11 | 23 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0002 | 0/1 | 2118 | 85 | 14 | 21 | 38 | 2 | 9 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0003 | 0/0 | 2118 | 25 | 9 | 5 | 6 | 1 | 4 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0004 | 0/0 | 2118 | 11 | 10 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0005 | 0/0 | 2118 | 6 | 6 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0006 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0007 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0008 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0009 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0010 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0011 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0012 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| c0013 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 9116 | 88 | 7 | 19 | 38 | 7 | 16 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0002 | 0/1 | 9117 | 56 | 1 | 14 | 33 | 0 | 7 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0003 | 0/0 | 9121 | 18 | 4 | 2 | 8 | 2 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0004 | 0/0 | 9121 | 12 | 0 | 3 | 6 | 0 | 3 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0005 | 0/0 | 9118 | 7 | 6 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0006 | 0/0 | 9116 | 7 | 0 | 0 | 7 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0007 | 0/0 | 9116 | 6 | 5 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0008 | 0/0 | 9117 | 6 | 0 | 1 | 5 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0009 | 0/0 | 9122 | 5 | 4 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0010 | 0/0 | 9117 | 5 | 0 | 0 | 3 | 0 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0011 | 0/0 | 9112 | 5 | 5 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0012 | 0/0 | 9122 | 5 | 0 | 5 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0013 | 0/0 | 9121 | 4 | 1 | 3 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0014 | 0/0 | 9126 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0015 | 0/0 | 9122 | 4 | 1 | 1 | 1 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0016 | 0/0 | 9121 | 4 | 0 | 2 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0017 | 0/0 | 9116 | 3 | 3 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0018 | 0/0 | 9117 | 3 | 1 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0019 | 0/0 | 9117 | 3 | 1 | 1 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0020 | 0/0 | 9108 | 3 | 1 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0021 | 0/0 | 9137 | 3 | 3 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0022 | 0/0 | 9118 | 2 | 0 | 1 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0023 | 0/0 | 9123 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0024 | 0/0 | 9117 | 2 | 1 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0025 | 0/0 | 9117 | 2 | 0 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0026 | 0/0 | 9118 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0027 | 0/0 | 9121 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0028 | 0/0 | 9125 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0029 | 0/0 | 9116 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0030 | 0/0 | 9116 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0031 | 0/0 | 9116 | 2 | 0 | 0 | 0 | 0 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0032 | 0/0 | 9112 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0033 | 0/0 | 9131 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0034 | 0/0 | 9122 | 2 | 1 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0035 | 0/0 | 9121 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0036 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0037 | 0/0 | 9117 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0038 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0039 | 0/0 | 9121 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0040 | 0/0 | 9121 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0041 | 0/0 | 9121 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0042 | 0/0 | 9121 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0043 | 0/0 | 9119 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0044 | 0/0 | 9119 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0045 | 0/0 | 9118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0046 | 0/0 | 9123 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0047 | 0/0 | 9123 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0048 | 0/0 | 9120 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0049 | 0/0 | 9121 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0050 | 0/0 | 9120 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0051 | 0/0 | 9119 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0052 | 0/0 | 9118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0053 | 0/0 | 9117 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0054 | 0/0 | 9123 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0055 | 0/0 | 9122 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0056 | 0/0 | 9122 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0057 | 0/0 | 9118 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0058 | 0/0 | 9117 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0059 | 0/0 | 9117 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0060 | 0/0 | 9116 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0061 | 0/0 | 9121 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0062 | 0/0 | 9121 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0063 | 0/0 | 9122 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0064 | 0/0 | 9120 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0065 | 0/0 | 9116 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0066 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0067 | 0/0 | 9116 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0068 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0069 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0070 | 0/0 | 9117 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0071 | 0/0 | 9121 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0072 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0073 | 0/0 | 9116 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0074 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0075 | 0/0 | 9115 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0076 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0077 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0078 | 0/0 | 9116 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0079 | 0/0 | 9117 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0080 | 0/0 | 9126 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0081 | 0/0 | 9118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0082 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0083 | 0/0 | 9117 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0084 | 0/0 | 9108 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0085 | 0/0 | 9118 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0086 | 0/0 | 9116 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0087 | 0/0 | 9112 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0088 | 0/0 | 9121 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0089 | 0/0 | 9130 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0090 | 0/0 | 9137 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0091 | 0/0 | 9120 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0092 | 0/0 | 9123 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0093 | 0/0 | 9122 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0094 | 0/0 | 9120 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0095 | 0/0 | 9122 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| t0096 | 0/0 | 9120 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 13 | 0 | 2 | 8 | 1 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0002 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0003 | 0/0 | 9 | 0 | 4 | 0 | 4 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0007 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0011 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2118 | 205 | 43 | 45 | 82 | 11 | 23 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002 | 0/1 | 2118 | 85 | 14 | 21 | 38 | 2 | 9 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003 | 0/0 | 2118 | 25 | 9 | 5 | 6 | 1 | 4 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004 | 0/0 | 2118 | 11 | 10 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0005 | 0/0 | 2118 | 6 | 6 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0007 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0009 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0010 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0002c0011 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0003c0008 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0004c0006 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0005c0012 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0006c0013 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 11233 | 88 | 7 | 19 | 38 | 7 | 16 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0003 | 0/0 | 11238 | 18 | 4 | 2 | 8 | 2 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0006 | 0/0 | 11233 | 7 | 0 | 0 | 7 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0007 | 0/0 | 11233 | 4 | 3 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0008 | 0/0 | 11234 | 5 | 0 | 1 | 4 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0010 | 0/0 | 11234 | 5 | 0 | 0 | 3 | 0 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0011 | 0/0 | 11229 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0012 | 0/0 | 11239 | 5 | 0 | 5 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0013 | 0/0 | 11238 | 4 | 1 | 3 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0015 | 0/0 | 11239 | 4 | 1 | 1 | 1 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0016 | 0/0 | 11238 | 4 | 0 | 2 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0017 | 0/0 | 11233 | 3 | 3 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0018 | 0/0 | 11234 | 3 | 1 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0019 | 0/0 | 11234 | 3 | 1 | 1 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0020 | 0/0 | 11225 | 3 | 1 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0021 | 0/0 | 11254 | 3 | 3 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0029 | 0/0 | 11233 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0030 | 0/0 | 11233 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0031 | 0/0 | 11233 | 2 | 0 | 0 | 0 | 0 | 2 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0033 | 0/0 | 11248 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0034 | 0/0 | 11239 | 2 | 1 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0035 | 0/0 | 11238 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0036 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0037 | 0/0 | 11234 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0038 | 0/0 | 11249 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0039 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0040 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0041 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0042 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0060 | 0/0 | 11233 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0064 | 0/0 | 11237 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0065 | 0/0 | 11233 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0066 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0067 | 0/0 | 11233 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0068 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0069 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0070 | 0/0 | 11234 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0071 | 0/0 | 11238 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0072 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0074 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0075 | 0/0 | 11232 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0076 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0077 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0078 | 0/0 | 11233 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0082 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0084 | 0/0 | 11225 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0086 | 0/0 | 11233 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0087 | 0/0 | 11229 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0089 | 0/0 | 11247 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0090 | 0/0 | 11254 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0092 | 0/0 | 11240 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0093 | 0/0 | 11239 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0094 | 0/0 | 11237 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0095 | 0/0 | 11239 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0001t0096 | 0/0 | 11237 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0002 | 0/1 | 11234 | 55 | 1 | 14 | 32 | 0 | 7 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0005 | 0/0 | 11235 | 7 | 6 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0007 | 0/0 | 11233 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0022 | 0/0 | 11235 | 2 | 0 | 1 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0024 | 0/0 | 11234 | 2 | 1 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0025 | 0/0 | 11234 | 2 | 0 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0026 | 0/0 | 11235 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0043 | 0/0 | 11236 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0044 | 0/0 | 11236 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0045 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0050 | 0/0 | 11237 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0051 | 0/0 | 11236 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0052 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0053 | 0/0 | 11234 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0057 | 0/0 | 11235 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0058 | 0/0 | 11234 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0059 | 0/0 | 11234 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0079 | 0/0 | 11234 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0081 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0083 | 0/0 | 11234 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0002t0085 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0004 | 0/0 | 11238 | 12 | 0 | 3 | 6 | 0 | 3 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0009 | 0/0 | 11239 | 5 | 4 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0027 | 0/0 | 11238 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0047 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0048 | 0/0 | 11237 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0055 | 0/0 | 11239 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0056 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0061 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0003t0088 | 0/0 | 11238 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0014 | 0/0 | 11243 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0023 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0028 | 0/0 | 11242 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0046 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0054 | 0/0 | 11240 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0062 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0004t0080 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0005t0011 | 0/0 | 11229 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0005t0032 | 0/0 | 11229 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0007t0063 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0009t0091 | 0/0 | 11237 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0001c0010t0008 | 0/0 | 11234 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0002c0011t0007 | 0/0 | 11233 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0003c0008t0073 | 0/0 | 11233 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0004c0006t0002 | 0/0 | 11234 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0005c0012t0023 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| a0006c0013t0049 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | copy fasta | chr9 | 78231075 | 78284690 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 2 | 6 | 1 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 4 | 0 | 4 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0008g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0010g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0012g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0012g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0012g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0012g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0013g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0015g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0015g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0015g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0015g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0016g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0016g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0016g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0017g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0018g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0019g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0019g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0020g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0020g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0021g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0021g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0029g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0030g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0030g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0031g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0031g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0033g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0033g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0034g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0034g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0035g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0035g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0036g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0037g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0038g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0039g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0040g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0041g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0042g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0060g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0064g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0065g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0066g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0067g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0068g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0069g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0070g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0071g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0072g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0074g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0075g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0076g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0077g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0078g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0082g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0084g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0086g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0087g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0089g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0090g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0092g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0093g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0094g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0095g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0001t0096g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0002 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0005g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0022g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0022g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0024g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0024g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0025g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0025g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0026g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0043g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0044g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0045g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0050g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0051g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0052g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0053g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0057g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0058g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0059g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0079g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0081g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0083g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0002t0085g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0009g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0027g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0027g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0047g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0048g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0055g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0056g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0061g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0003t0088g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0014g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0014g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0023g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0028g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0028g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0046g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0054g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0062g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0004t0080g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0005t0011g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0005t0032g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0005t0032g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0007t0063g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0009t0091g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0001c0010t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0002c0011t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0003c0008t0073g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0004c0006t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0005c0012t0023g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| a0006c0013t0049g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0083 | g0066 | EUR | GBR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00323 | hp1 | a0001 | c0001 | t0019 | g0136 | EUR | FIN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00323 | hp2 | a0001 | c0001 | t0015 | g0242 | EUR | FIN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00408 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00438 | hp1 | a0001 | c0002 | t0022 | g0052 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00438 | hp2 | a0001 | c0002 | t0085 | g0046 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00621 | hp1 | a0001 | c0002 | t0059 | g0076 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00642 | hp2 | a0001 | c0001 | t0089 | g0094 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00673 | hp2 | a0001 | c0001 | t0069 | g0146 | EAS | CHS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00735 | hp1 | a0001 | c0001 | t0092 | g0236 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0090 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0017 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01069 | hp1 | a0001 | c0003 | t0048 | g0206 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01069 | hp2 | a0001 | c0001 | t0016 | g0247 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01070 | hp1 | a0001 | c0001 | t0064 | g0153 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01070 | hp2 | a0001 | c0002 | t0057 | g0038 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01071 | hp2 | a0001 | c0001 | t0016 | g0017 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01074 | hp1 | a0001 | c0003 | t0004 | g0205 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0179 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01168 | hp2 | a0001 | c0001 | t0020 | g0148 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0024 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01192 | hp2 | a0001 | c0003 | t0009 | g0218 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01243 | hp1 | a0001 | c0001 | t0065 | g0172 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0067 | AMR | PUR | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01255 | hp1 | a0001 | c0004 | t0054 | g0119 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01256 | hp2 | a0001 | c0001 | t0012 | g0231 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01257 | hp2 | a0001 | c0002 | t0025 | g0042 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01258 | hp2 | a0001 | c0002 | t0025 | g0055 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0006 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0225 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01346 | hp1 | a0001 | c0001 | t0019 | g0028 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01358 | hp1 | a0001 | c0001 | t0013 | g0006 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01433 | hp2 | a0001 | c0002 | t0053 | g0010 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0237 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0248 | EUR | IBS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01516 | hp1 | a0001 | c0002 | t0024 | g0010 | EUR | IBS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0224 | EUR | IBS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01891 | hp1 | a0001 | c0001 | t0021 | g0012 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01891 | hp2 | a0001 | c0001 | t0060 | g0105 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01952 | hp1 | a0001 | c0001 | t0040 | g0006 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01978 | hp1 | a0001 | c0001 | t0037 | g0034 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01981 | hp1 | a0001 | c0002 | t0050 | g0048 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01981 | hp2 | a0001 | c0001 | t0012 | g0226 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01993 | hp1 | a0001 | c0003 | t0004 | g0176 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02015 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02027 | hp2 | a0001 | c0001 | t0010 | g0192 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02040 | hp2 | a0001 | c0001 | t0030 | g0133 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02055 | hp1 | a0001 | c0003 | t0027 | g0208 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02055 | hp2 | a0001 | c0005 | t0011 | g0008 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02056 | hp1 | a0001 | c0001 | t0077 | g0117 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02074 | hp2 | a0001 | c0001 | t0086 | g0189 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02080 | hp1 | a0001 | c0001 | t0016 | g0232 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0194 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02083 | hp1 | a0001 | c0003 | t0004 | g0214 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02129 | hp1 | a0001 | c0001 | t0015 | g0230 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02148 | hp2 | a0001 | c0001 | t0093 | g0234 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02165 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | CDX | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0104 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02257 | hp2 | a0001 | c0004 | t0014 | g0030 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02258 | hp1 | a0001 | c0005 | t0011 | g0008 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02258 | hp2 | a0001 | c0007 | t0063 | g0216 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02273 | hp1 | a0001 | c0001 | t0042 | g0006 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02273 | hp2 | a0001 | c0001 | t0012 | g0017 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02300 | hp1 | a0001 | c0001 | t0013 | g0006 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02300 | hp2 | a0001 | c0002 | t0022 | g0002 | AMR | PEL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02572 | hp1 | a0001 | c0002 | t0024 | g0077 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02572 | hp2 | a0001 | c0004 | t0014 | g0115 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02615 | hp1 | a0001 | c0004 | t0023 | g0213 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02622 | hp1 | a0001 | c0001 | t0033 | g0097 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02630 | hp1 | a0001 | c0003 | t0061 | g0175 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02630 | hp2 | a0001 | c0002 | t0005 | g0088 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02683 | hp1 | a0001 | c0003 | t0004 | g0031 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02717 | hp1 | a0001 | c0003 | t0009 | g0032 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02717 | hp2 | a0001 | c0005 | t0011 | g0008 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02723 | hp2 | a0001 | c0004 | t0046 | g0221 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02809 | hp1 | a0001 | c0001 | t0087 | g0102 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0243 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02818 | hp1 | a0001 | c0001 | t0021 | g0095 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02818 | hp2 | a0001 | c0004 | t0014 | g0023 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0024 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02886 | hp2 | a0001 | c0005 | t0011 | g0008 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02895 | hp2 | a0001 | c0005 | t0032 | g0103 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02896 | hp2 | a0001 | c0002 | t0081 | g0040 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02897 | hp1 | a0001 | c0005 | t0032 | g0127 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02922 | hp1 | a0001 | c0001 | t0041 | g0108 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0012 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02965 | hp1 | a0001 | c0001 | t0038 | g0251 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02965 | hp2 | a0006 | c0013 | t0049 | g0203 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02970 | hp1 | a0001 | c0001 | t0034 | g0238 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02970 | hp2 | a0001 | c0003 | t0056 | g0202 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02976 | hp1 | a0001 | c0001 | t0035 | g0099 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03041 | hp2 | a0001 | c0002 | t0007 | g0051 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03139 | hp1 | a0001 | c0001 | t0090 | g0096 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03139 | hp2 | a0001 | c0001 | t0035 | g0098 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ESN | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03209 | hp1 | a0001 | c0004 | t0028 | g0220 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03209 | hp2 | a0001 | c0003 | t0009 | g0032 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03225 | hp1 | a0001 | c0002 | t0045 | g0005 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0009 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0009 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03453 | hp2 | a0001 | c0003 | t0027 | g0210 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03486 | hp1 | a0002 | c0011 | t0007 | g0126 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03486 | hp2 | a0005 | c0012 | t0023 | g0116 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03490 | hp1 | a0001 | c0001 | t0031 | g0139 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03492 | hp1 | a0001 | c0001 | t0010 | g0001 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03492 | hp2 | a0001 | c0001 | t0031 | g0112 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03540 | hp1 | a0001 | c0004 | t0014 | g0023 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03579 | hp2 | a0001 | c0001 | t0096 | g0123 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03688 | hp1 | a0001 | c0002 | t0079 | g0011 | SAS | STU | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0079 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03834 | hp1 | a0001 | c0003 | t0004 | g0212 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03834 | hp2 | a0001 | c0001 | t0084 | g0160 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03927 | hp2 | a0001 | c0003 | t0055 | g0177 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0131 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG04115 | hp1 | a0001 | c0002 | t0051 | g0074 | SAS | STU | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG04115 | hp2 | a0001 | c0003 | t0004 | g0207 | SAS | STU | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | YRI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18906 | hp1 | a0001 | c0003 | t0009 | g0217 | AFR | YRI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18906 | hp2 | a0003 | c0008 | t0073 | g0161 | AFR | YRI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18944 | hp2 | a0001 | c0002 | t0026 | g0002 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18949 | hp2 | a0001 | c0001 | t0068 | g0185 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18951 | hp2 | a0001 | c0001 | t0075 | g0178 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18953 | hp1 | a0001 | c0001 | t0082 | g0137 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18954 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18954 | hp2 | a0004 | c0006 | t0002 | g0021 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18960 | hp1 | a0001 | c0001 | t0034 | g0091 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18966 | hp2 | a0001 | c0003 | t0004 | g0211 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18969 | hp1 | a0001 | c0001 | t0076 | g0014 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18971 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18984 | hp2 | a0001 | c0003 | t0004 | g0204 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18985 | hp1 | a0001 | c0002 | t0058 | g0084 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18985 | hp2 | a0001 | c0001 | t0072 | g0013 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18989 | hp1 | a0001 | c0001 | t0070 | g0182 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18989 | hp2 | a0001 | c0001 | t0095 | g0240 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18991 | hp1 | a0001 | c0001 | t0036 | g0147 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0162 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18994 | hp1 | a0001 | c0001 | t0071 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18999 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19005 | hp1 | a0001 | c0001 | t0074 | g0144 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0196 | AFR | LWK | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19030 | hp2 | a0001 | c0001 | t0078 | g0195 | AFR | LWK | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19043 | hp1 | a0001 | c0004 | t0028 | g0219 | AFR | LWK | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19043 | hp2 | a0001 | c0001 | t0094 | g0245 | AFR | LWK | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19068 | hp1 | a0001 | c0001 | t0018 | g0004 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19074 | hp1 | a0001 | c0001 | t0030 | g0149 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19076 | hp2 | a0001 | c0010 | t0008 | g0157 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19079 | hp1 | a0001 | c0002 | t0026 | g0075 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19085 | hp1 | a0001 | c0001 | t0066 | g0167 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19085 | hp2 | a0001 | c0001 | t0016 | g0223 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0111 | AFR | YRI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA19240 | hp2 | a0001 | c0001 | t0029 | g0009 | AFR | YRI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20129 | hp1 | a0001 | c0002 | t0052 | g0041 | AFR | ASW | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20805 | hp1 | a0001 | c0003 | t0088 | g0174 | EUR | TSI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0059 | SAS | GIH | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG01123 | hp2 | a0001 | c0003 | t0004 | g0031 | AMR | CLM | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02109 | hp1 | a0001 | c0001 | t0067 | g0199 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02109 | hp2 | a0001 | c0002 | t0043 | g0005 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0101 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02486 | hp2 | a0001 | c0001 | t0033 | g0012 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02559 | hp1 | a0001 | c0002 | t0044 | g0089 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG02559 | hp2 | a0001 | c0004 | t0080 | g0030 | AFR | ACB | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03471 | hp1 | a0001 | c0009 | t0091 | g0201 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG03471 | hp2 | a0001 | c0004 | t0062 | g0222 | AFR | MSL | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| HG06807 | hp2 | a0001 | c0001 | t0029 | g0009 | AFR | USA | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0106 | AFR | USA | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA20300 | hp2 | a0001 | c0003 | t0009 | g0215 | AFR | USA | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA21309 | hp1 | a0001 | c0003 | t0047 | g0209 | AFR | LWK | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| NA21309 | hp2 | a0001 | c0001 | t0039 | g0107 | AFR | LWK | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0069 | REF | REF | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0156 | REF | REF | CEP78_chr9_78231075_78284690 | CEP78 | chr9 | 78231075 | 78284690 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78236385
|
C | T | 1 | a0006 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.35C>T | p.Ala12Val | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | 311/11233 | 35/2118 | 12/705 | chr9 | 78236385 | ||
| chr9:78240062
|
C | T | 1 | a0005 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.293C>T | p.Ala98Val | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 2/17 | 569/11233 | 293/2118 | 98/705 | chr9 | 78240062 | ||
| chr9:78243568
|
A | G | 1 | a0004 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.710A>G | p.Asn237Ser | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/17 | 986/11233 | 710/2118 | 237/705 | chr9 | 78243568 | ||
| chr9:78246741
|
C | G | 1 | a0002 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.851C>G | p.Thr284Arg | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/17 | 1127/11233 | 851/2118 | 284/705 | chr9 | 78246741 | ||
| chr9:78248353
|
G | C | 1 | a0003 | 1 | NA18906.hp2 | missense_variant&splice_region_variant | MODERATE | c.955G>C | p.Glu319Gln | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 7/17 | 1231/11233 | 955/2118 | 319/705 | chr9 | 78248353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78236434
|
G | C | 2 | a0001c0002a0004c0006 | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
synonymous_variant | LOW | c.84G>C | p.Ser28Ser | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | 360/11233 | 84/2118 | 28/705 | chr9 | 78236434 | ||
| chr9:78236476
|
G | A | 1 | a0001c0007 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.126G>A | p.Val42Val | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | 402/11233 | 126/2118 | 42/705 | chr9 | 78236476 | ||
| chr9:78264233
|
C | T | 3 | a0001c0003a0001c0007a0006c0013 | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
synonymous_variant | LOW | c.1542C>T | p.Ile514Ile | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/17 | 1818/11233 | 1542/2118 | 514/705 | chr9 | 78264233 | ||
| chr9:78265483
|
G | T | 1 | a0001c0010 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.1737G>T | p.Ala579Ala | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/17 | 2013/11233 | 1737/2118 | 579/705 | chr9 | 78265483 | ||
| chr9:78265534
|
A | G | 1 | a0001c0005 | 6 | HG02055.hp2 HG02258.hp1 HG02717.hp2 others(3): Show |
synonymous_variant | LOW | c.1788A>G | p.Gln596Gln | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/17 | 2064/11233 | 1788/2118 | 596/705 | chr9 | 78265534 | ||
| chr9:78266603
|
T | C | 2 | a0001c0004a0005c0012 | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
synonymous_variant | LOW | c.2007T>C | p.Cys669Cys | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/17 | 2283/11233 | 2007/2118 | 669/705 | chr9 | 78266603 | ||
| chr9:78266673
|
A | C | 1 | a0001c0009 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2077A>C | p.Arg693Arg | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/17 | 2353/11233 | 2077/2118 | 693/705 | chr9 | 78266673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78236103
|
A | G | 1 | a0001c0001t0096 | 1 | HG03579.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-248A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | chr9 | 78236103 | ||||||
| chr9:78236108
|
G | T | 1 | a0001c0001t0035 | 2 | HG02976.hp1 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-243G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | 243 | chr9 | 78236108 | |||||
| chr9:78236227
|
C | T | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(6): Show | 37 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-124C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | chr9 | 78236227 | ||||||
| chr9:78236233
|
G | A | 1 | a0001c0001t0036 | 1 | NA18991.hp1 | 5_prime_UTR_variant | MODIFIER | c.-118G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/17 | 118 | chr9 | 78236233 | |||||
| chr9:78270864
|
A | T | 1 | a0001c0009t0091 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 13 | chr9 | 78270864 | |||||
| chr9:78271176
|
G | A | 1 | a0001c0001t0037 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 325 | chr9 | 78271176 | |||||
| chr9:78271480
|
A | G | 4 | a0001c0001t0021a0001c0001t0033a0001c0001t0089others(1): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*629A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 629 | chr9 | 78271480 | |||||
| chr9:78271525
|
ACACT | A | 4 | a0001c0001t0011a0001c0001t0087a0001c0005t0011others(1): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*677_*680delCTCA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 677 | INFO_REALIGN_3_PRIME | chr9 | 78271525 | ||||
| chr9:78271527
|
A | C | 1 | a0001c0003t0088 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 676 | chr9 | 78271527 | |||||
| chr9:78271776
|
T | C | 1 | a0001c0001t0038 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 925 | chr9 | 78271776 | |||||
| chr9:78271785
|
T | C | 1 | a0001c0001t0039 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 934 | chr9 | 78271785 | |||||
| chr9:78271851
|
C | T | 2 | a0001c0001t0086a0001c0002t0085 | 2 | HG00438.hp2 HG02074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1000C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1000 | chr9 | 78271851 | |||||
| chr9:78271892
|
CTTTTCTT others(1): Show |
C | 3 | a0001c0001t0020a0001c0001t0084a0001c0009t0091 | 5 | HG01168.hp2 HG01169.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1062_*1069delCTTT others(4): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1062 | INFO_REALIGN_3_PRIME | chr9 | 78271892 | ||||
| chr9:78271913
|
C | A | 19 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(16): Show | 54 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1062C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1062 | chr9 | 78271913 | |||||
| chr9:78271913
|
C | CT | 2 | a0001c0001t0008a0001c0010t0008 | 6 | HG01255.hp2 HG02080.hp2 NA18952.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1072dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1073 | INFO_REALIGN_3_PRIME | chr9 | 78271913 | ||||
| chr9:78272041
|
C | G | 1 | a0001c0002t0083 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1190 | chr9 | 78272041 | |||||
| chr9:78272176
|
C | T | 1 | a0001c0001t0082 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1325C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1325 | chr9 | 78272176 | |||||
| chr9:78272177
|
C | T | 1 | a0001c0001t0082 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1326C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1326 | chr9 | 78272177 | |||||
| chr9:78272224
|
G | A | 1 | a0001c0001t0040 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1373 | chr9 | 78272224 | |||||
| chr9:78272337
|
G | A | 4 | a0001c0001t0021a0001c0001t0033a0001c0001t0089others(1): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1486G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1486 | chr9 | 78272337 | |||||
| chr9:78272365
|
T | C | 5 | a0001c0001t0035a0001c0002t0005a0001c0002t0043others(2): Show | 12 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1514T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1514 | chr9 | 78272365 | |||||
| chr9:78272476
|
T | C | 4 | a0001c0001t0021a0001c0001t0033a0001c0001t0089others(1): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1625T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1625 | chr9 | 78272476 | |||||
| chr9:78272493
|
C | G | 1 | a0001c0002t0081 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1642C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1642 | chr9 | 78272493 | |||||
| chr9:78272509
|
A | G | 1 | a0001c0004t0080 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1658A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1658 | chr9 | 78272509 | |||||
| chr9:78272548
|
C | T | 4 | a0001c0001t0021a0001c0001t0033a0001c0001t0089others(1): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1697C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1697 | chr9 | 78272548 | |||||
| chr9:78272561
|
T | C | 1 | a0001c0004t0046 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1710T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1710 | chr9 | 78272561 | |||||
| chr9:78272637
|
A | G | 1 | a0001c0002t0079 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1786A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1786 | chr9 | 78272637 | |||||
| chr9:78272662
|
T | G | 1 | a0001c0001t0096 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1811T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1811 | chr9 | 78272662 | |||||
| chr9:78272732
|
C | T | 3 | a0001c0001t0013a0001c0001t0040a0001c0001t0042 | 6 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1881C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1881 | chr9 | 78272732 | |||||
| chr9:78272776
|
A | T | 1 | a0001c0001t0078 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1925 | chr9 | 78272776 | |||||
| chr9:78272812
|
G | A | 1 | a0001c0003t0047 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1961G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 1961 | chr9 | 78272812 | |||||
| chr9:78272967
|
G | A | 73 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(70): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2116G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2116 | chr9 | 78272967 | |||||
| chr9:78273035
|
T | C | 1 | a0001c0001t0096 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2184T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2184 | chr9 | 78273035 | |||||
| chr9:78273085
|
A | T | 1 | a0001c0001t0077 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2234A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2234 | chr9 | 78273085 | |||||
| chr9:78273320
|
T | G | 1 | a0001c0001t0065 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2469T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2469 | chr9 | 78273320 | |||||
| chr9:78273375
|
C | A | 73 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(70): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2524C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2524 | chr9 | 78273375 | |||||
| chr9:78273415
|
T | A | 1 | a0001c0001t0066 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2564T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2564 | chr9 | 78273415 | |||||
| chr9:78273426
|
A | G | 1 | a0001c0001t0076 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2575A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2575 | chr9 | 78273426 | |||||
| chr9:78273447
|
T | C | 1 | a0001c0003t0048 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2596T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2596 | chr9 | 78273447 | |||||
| chr9:78273456
|
G | A | 1 | a0006c0013t0049 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2605G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2605 | chr9 | 78273456 | |||||
| chr9:78273460
|
G | A | 5 | a0001c0001t0013a0001c0001t0039a0001c0001t0040others(2): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2609G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2609 | chr9 | 78273460 | |||||
| chr9:78273579
|
C | CA | 25 | a0001c0001t0010a0001c0001t0015a0001c0001t0037others(22): Show | 92 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2746dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2747 | INFO_REALIGN_3_PRIME | chr9 | 78273579 | ||||
| chr9:78273579
|
C | CAA | 5 | a0001c0002t0005a0001c0002t0022a0001c0002t0045others(2): Show | 12 | HG00438.hp1 HG01243.hp2 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2745_*2746dupAA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2747 | INFO_REALIGN_3_PRIME | chr9 | 78273579 | ||||
| chr9:78273579
|
C | CAAA | 8 | a0001c0001t0021a0001c0001t0033a0001c0001t0089others(5): Show | 11 | HG00642.hp2 HG01891.hp1 HG01981.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2744_*2746dupAAA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2747 | INFO_REALIGN_3_PRIME | chr9 | 78273579 | ||||
| chr9:78273579
|
CA | C | 10 | a0001c0001t0013a0001c0001t0035a0001c0001t0039others(7): Show | 14 | HG01070.hp1 HG01261.hp1 HG01358.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2746delA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2746 | INFO_REALIGN_3_PRIME | chr9 | 78273579 | ||||
| chr9:78273618
|
A | T | 1 | a0001c0007t0063 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2767A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2767 | chr9 | 78273618 | |||||
| chr9:78273800
|
G | A | 1 | a0001c0001t0030 | 2 | HG02040.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2949G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2949 | chr9 | 78273800 | |||||
| chr9:78273817
|
G | C | 1 | a0001c0001t0060 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 2966 | chr9 | 78273817 | |||||
| chr9:78274120
|
A | T | 3 | a0001c0001t0017a0001c0001t0029a0001c0001t0060 | 6 | HG01891.hp2 HG02486.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3269A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 3269 | chr9 | 78274120 | |||||
| chr9:78274163
|
G | A | 1 | a0001c0002t0053 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3312G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 3312 | chr9 | 78274163 | |||||
| chr9:78274224
|
C | T | 2 | a0001c0004t0028a0001c0004t0062 | 3 | HG03209.hp1 HG03471.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3373C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 3373 | chr9 | 78274224 | |||||
| chr9:78274475
|
T | A | 1 | a0001c0003t0061 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3624T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 3624 | chr9 | 78274475 | |||||
| chr9:78274667
|
T | A | 1 | a0001c0001t0038 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3816T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 3816 | chr9 | 78274667 | |||||
| chr9:78274771
|
C | A | 5 | a0001c0001t0067a0001c0004t0023a0001c0004t0046others(2): Show | 5 | HG01255.hp1 HG02109.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3920C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 3920 | chr9 | 78274771 | |||||
| chr9:78274883
|
A | G | 15 | a0001c0001t0074a0001c0002t0002a0001c0002t0022others(12): Show | 72 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4032A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4032 | chr9 | 78274883 | |||||
| chr9:78275000
|
C | T | 1 | a0003c0008t0073 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4149C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4149 | chr9 | 78275000 | |||||
| chr9:78275110
|
C | T | 1 | a0001c0005t0032 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4259C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4259 | chr9 | 78275110 | |||||
| chr9:78275333
|
G | A | 8 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(5): Show | 36 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4482G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4482 | chr9 | 78275333 | |||||
| chr9:78275466
|
T | G | 21 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(18): Show | 56 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*4615T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4615 | chr9 | 78275466 | |||||
| chr9:78275606
|
C | CA | 23 | a0001c0001t0013a0001c0001t0018a0001c0001t0039others(20): Show | 40 | HG00408.hp2 HG00735.hp1 HG01069.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4774dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4775 | INFO_REALIGN_3_PRIME | chr9 | 78275606 | ||||
| chr9:78275606
|
C | CAAAA | 3 | a0001c0004t0014a0001c0004t0028a0001c0004t0080 | 7 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4771_*4774dupAAAA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4775 | INFO_REALIGN_3_PRIME | chr9 | 78275606 | ||||
| chr9:78275606
|
C | CAAAAAA | 4 | a0001c0001t0021a0001c0001t0089a0001c0001t0090others(1): Show | 6 | HG00642.hp2 HG01891.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4769_*4774dupAAAA others(2): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4775 | INFO_REALIGN_3_PRIME | chr9 | 78275606 | ||||
| chr9:78275681
|
A | G | 1 | a0001c0001t0035 | 2 | HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4830A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4830 | chr9 | 78275681 | |||||
| chr9:78275782
|
C | A | 5 | a0001c0001t0013a0001c0001t0039a0001c0001t0040others(2): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4931C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 4931 | chr9 | 78275782 | |||||
| chr9:78275861
|
C | T | 2 | a0001c0001t0029a0001c0001t0060 | 3 | HG01891.hp2 HG06807.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5010C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5010 | chr9 | 78275861 | |||||
| chr9:78276103
|
T | G | 1 | a0001c0004t0054 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5252T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5252 | chr9 | 78276103 | |||||
| chr9:78276113
|
G | A | 1 | a0001c0001t0064 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5262G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5262 | chr9 | 78276113 | |||||
| chr9:78276140
|
T | C | 2 | a0001c0002t0043a0001c0002t0045 | 2 | HG02109.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5289T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5289 | chr9 | 78276140 | |||||
| chr9:78276167
|
A | C | 1 | a0001c0001t0006 | 7 | NA18950.hp1 NA18953.hp2 NA18970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5316A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5316 | chr9 | 78276167 | |||||
| chr9:78276173
|
A | T | 1 | a0001c0001t0031 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5322A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5322 | chr9 | 78276173 | |||||
| chr9:78276174
|
T | G | 1 | a0001c0001t0068 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5323T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5323 | chr9 | 78276174 | |||||
| chr9:78276253
|
G | A | 1 | a0001c0001t0038 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5402G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5402 | chr9 | 78276253 | |||||
| chr9:78276500
|
G | A | 1 | a0001c0001t0035 | 2 | HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5649G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5649 | chr9 | 78276500 | |||||
| chr9:78276528
|
C | T | 1 | a0001c0002t0059 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5677C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5677 | chr9 | 78276528 | |||||
| chr9:78276537
|
A | G | 6 | a0001c0001t0013a0001c0001t0035a0001c0001t0039others(3): Show | 10 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5686A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5686 | chr9 | 78276537 | |||||
| chr9:78276584
|
T | C | 1 | a0001c0001t0069 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5733T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5733 | chr9 | 78276584 | |||||
| chr9:78276612
|
AGT | A | 8 | a0001c0003t0004a0001c0003t0027a0001c0003t0048others(5): Show | 20 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5766_*5767delGT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5766 | INFO_REALIGN_3_PRIME | chr9 | 78276612 | ||||
| chr9:78276679
|
C | T | 2 | a0001c0001t0012a0001c0001t0016 | 9 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5828C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5828 | chr9 | 78276679 | |||||
| chr9:78276788
|
G | A | 1 | a0001c0001t0070 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5937G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5937 | chr9 | 78276788 | |||||
| chr9:78276813
|
A | C | 1 | a0001c0001t0087 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5962A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 5962 | chr9 | 78276813 | |||||
| chr9:78276926
|
A | T | 1 | a0001c0001t0072 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6075A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6075 | chr9 | 78276926 | |||||
| chr9:78277008
|
G | T | 1 | a0001c0002t0053 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6157G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6157 | chr9 | 78277008 | |||||
| chr9:78277050
|
A | G | 1 | a0001c0002t0058 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6199A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6199 | chr9 | 78277050 | |||||
| chr9:78277149
|
T | A | 1 | a0001c0001t0096 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6298T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6298 | chr9 | 78277149 | |||||
| chr9:78277503
|
C | T | 1 | a0001c0001t0038 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6652C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6652 | chr9 | 78277503 | |||||
| chr9:78277697
|
T | A | 1 | a0001c0001t0096 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6846T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6846 | chr9 | 78277697 | |||||
| chr9:78277781
|
A | G | 1 | a0001c0001t0037 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6930A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 6930 | chr9 | 78277781 | |||||
| chr9:78277945
|
C | T | 1 | a0001c0001t0038 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7094C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7094 | chr9 | 78277945 | |||||
| chr9:78278020
|
A | G | 1 | a0001c0001t0035 | 2 | HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7169A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7169 | chr9 | 78278020 | |||||
| chr9:78278136
|
A | T | 3 | a0001c0003t0027a0001c0003t0056a0006c0013t0049 | 4 | HG02055.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7285A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7285 | chr9 | 78278136 | |||||
| chr9:78278280
|
A | ATTTCC | 7 | a0001c0001t0021a0001c0001t0033a0001c0001t0038others(4): Show | 10 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7431_*7432insTCCT others(1): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7432 | INFO_REALIGN_3_PRIME | chr9 | 78278280 | ||||
| chr9:78278288
|
T | C | 1 | a0001c0009t0091 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7437T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7437 | chr9 | 78278288 | |||||
| chr9:78278450
|
C | A | 4 | a0001c0001t0021a0001c0001t0033a0001c0001t0089others(1): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7599C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7599 | chr9 | 78278450 | |||||
| chr9:78278474
|
A | C | 4 | a0001c0001t0011a0001c0001t0087a0001c0005t0011others(1): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7623A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7623 | chr9 | 78278474 | |||||
| chr9:78278537
|
T | C | 1 | a0001c0002t0025 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7686T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7686 | chr9 | 78278537 | |||||
| chr9:78278577
|
G | T | 1 | a0001c0001t0090 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7726G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7726 | chr9 | 78278577 | |||||
| chr9:78278679
|
C | T | 1 | a0001c0001t0042 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7828C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7828 | chr9 | 78278679 | |||||
| chr9:78278848
|
A | G | 5 | a0001c0001t0013a0001c0001t0039a0001c0001t0040others(2): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7997A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 7997 | chr9 | 78278848 | |||||
| chr9:78278960
|
G | A | 1 | a0001c0001t0035 | 2 | HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8109G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8109 | chr9 | 78278960 | |||||
| chr9:78279066
|
G | GA | 4 | a0001c0001t0019a0001c0001t0070a0001c0002t0026others(1): Show | 7 | HG00323.hp1 HG00438.hp2 HG01346.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8229dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8230 | INFO_REALIGN_3_PRIME | chr9 | 78279066 | ||||
| chr9:78279066
|
G | GAAAAA | 22 | a0001c0001t0003a0001c0001t0013a0001c0001t0015others(19): Show | 52 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8225_*8229dupAAAA others(1): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8230 | INFO_REALIGN_3_PRIME | chr9 | 78279066 | ||||
| chr9:78279066
|
G | GAAAAAA | 14 | a0001c0001t0012a0001c0001t0034a0001c0001t0035others(11): Show | 36 | HG00408.hp2 HG00738.hp2 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8224_*8229dupAAAA others(2): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8230 | INFO_REALIGN_3_PRIME | chr9 | 78279066 | ||||
| chr9:78279066
|
G | GAAAAAAA | 3 | a0001c0001t0021a0001c0001t0033a0001c0001t0090 | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8223_*8229dupAAAA others(3): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8230 | INFO_REALIGN_3_PRIME | chr9 | 78279066 | ||||
| chr9:78279066
|
G | GAAAAAAA others(4): Show |
1 | a0001c0001t0038 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8219_*8229dupAAAA others(7): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8230 | INFO_REALIGN_3_PRIME | chr9 | 78279066 | ||||
| chr9:78279268
|
T | C | 4 | a0001c0001t0011a0001c0001t0087a0001c0005t0011others(1): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8417T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8417 | chr9 | 78279268 | |||||
| chr9:78279368
|
A | G | 2 | a0001c0001t0096a0001c0009t0091 | 2 | HG03471.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8517A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8517 | chr9 | 78279368 | |||||
| chr9:78279427
|
A | G | 4 | a0001c0004t0023a0001c0004t0046a0001c0004t0054others(1): Show | 4 | HG01255.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8576A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 17/17 | 8576 | chr9 | 78279427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78236611
|
G | A | 72 | a0001c0002t0002g0002a0001c0002t0002g0010a0001c0002t0002g0011others(69): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
splice_region_variant&intron_variant | LOW | c.253+8G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236611 | ||||||
| chr9:78236623
|
A | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253+20A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236623 | ||||||
| chr9:78236630
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG01952.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+27C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236630 | ||||||
| chr9:78236732
|
G | A | 3 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0034g0091 | 3 | NA18951.hp1 NA18960.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.253+129G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236732 | ||||||
| chr9:78236817
|
A | G | 33 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(30): Show | 37 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.253+214A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236817 | ||||||
| chr9:78236958
|
T | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+355T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236958 | ||||||
| chr9:78236959
|
C | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+356C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236959 | ||||||
| chr9:78236962
|
C | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253+359C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78236962 | ||||||
| chr9:78236969
|
C | CT | 22 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0180others(19): Show | 25 | HG00140.hp1 HG00735.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.253+395dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTT | 11 | a0001c0001t0001g0029a0001c0001t0001g0197a0001c0001t0001g0198others(8): Show | 12 | HG01070.hp2 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+394_253+395dup others(2): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTT | 50 | a0001c0001t0001g0200a0001c0001t0021g0012a0001c0001t0021g0095others(47): Show | 64 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.253+393_253+395dup others(3): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTT | 22 | a0001c0001t0033g0097a0001c0002t0002g0011a0001c0002t0002g0072others(19): Show | 23 | HG00558.hp1 HG00621.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.253+392_253+395dup others(4): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTTTT | 10 | a0001c0002t0002g0090a0001c0003t0004g0031a0001c0003t0004g0204others(7): Show | 11 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+390_253+395dup others(6): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTTTTT | 7 | a0001c0003t0004g0016a0001c0003t0004g0211a0001c0003t0004g0212others(4): Show | 10 | HG00408.hp2 HG02015.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+389_253+395dup others(7): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTTTTT others(1): Show |
6 | a0001c0003t0004g0214a0001c0003t0009g0215a0001c0003t0009g0217others(3): Show | 6 | HG01192.hp2 HG02083.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+388_253+395dup others(8): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTTTTT others(3): Show |
2 | a0001c0004t0028g0219a0001c0004t0028g0220 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.253+386_253+395dup others(10): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTTTTT others(4): Show |
1 | a0001c0004t0046g0221 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.253+385_253+395dup others(11): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
C | CTTTTTTT others(9): Show |
1 | a0001c0004t0062g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.253+380_253+395dup others(16): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
CT | C | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0113others(3): Show | 6 | HG02602.hp1 HG03017.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+395delT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
CTTTTT | C | 30 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(27): Show | 34 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.253+391_253+395del others(5): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0011g0104a0001c0001t0013g0006a0001c0001t0013g0106others(11): Show | 21 | HG01261.hp1 HG01358.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.253+388_253+395del others(8): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.253+386_253+395del others(10): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78236969
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.253+382_253+395del others(14): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78236969 | |||||
| chr9:78237090
|
C | T | 2 | a0001c0001t0021g0012a0001c0001t0033g0012 | 3 | HG01891.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.253+487C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237090 | ||||||
| chr9:78237183
|
G | C | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+580G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237183 | ||||||
| chr9:78237222
|
C | T | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+619C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237222 | ||||||
| chr9:78237265
|
G | A | 33 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(30): Show | 37 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.253+662G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237265 | ||||||
| chr9:78237306
|
A | G | 72 | a0001c0002t0002g0002a0001c0002t0002g0010a0001c0002t0002g0011others(69): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.253+703A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237306 | ||||||
| chr9:78237314
|
T | C | 5 | a0001c0004t0014g0023a0001c0004t0014g0115a0001c0004t0028g0219others(2): Show | 6 | HG02572.hp2 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.253+711T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237314 | ||||||
| chr9:78237487
|
C | T | 1 | a0001c0003t0004g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.253+884C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237487 | ||||||
| chr9:78237520
|
C | G | 1 | a0001c0002t0002g0071 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.253+917C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237520 | ||||||
| chr9:78237701
|
T | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+1098T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237701 | ||||||
| chr9:78237876
|
G | A | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.253+1273G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237876 | ||||||
| chr9:78237880
|
G | T | 23 | a0001c0003t0004g0016a0001c0003t0004g0031a0001c0003t0004g0176others(20): Show | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.253+1277G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237880 | ||||||
| chr9:78237955
|
C | CA | 24 | a0001c0001t0001g0015a0001c0001t0001g0150a0001c0001t0001g0152others(21): Show | 28 | HG00673.hp2 HG01070.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.253+1372dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78237955 | |||||
| chr9:78237955
|
C | CAA | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(78): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.253+1371_253+1372d others(4): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78237955 | |||||
| chr9:78237955
|
C | CAAA | 76 | a0001c0001t0001g0118a0001c0001t0003g0018a0001c0001t0003g0092others(73): Show | 88 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.253+1370_253+1372d others(5): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78237955 | |||||
| chr9:78237955
|
C | CAAAA | 21 | a0001c0001t0003g0224a0001c0001t0003g0227a0001c0001t0003g0228others(18): Show | 23 | HG00438.hp2 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.253+1369_253+1372d others(6): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78237955 | |||||
| chr9:78237955
|
CAAAAA | C | 23 | a0001c0003t0004g0016a0001c0003t0004g0031a0001c0003t0004g0176others(20): Show | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.253+1368_253+1372d others(7): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78237955 | |||||
| chr9:78237986
|
G | A | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+1383G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78237986 | ||||||
| chr9:78238038
|
T | C | 1 | a0001c0002t0002g0019 | 2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.253+1435T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238038 | ||||||
| chr9:78238124
|
T | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253+1521T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238124 | ||||||
| chr9:78238125
|
C | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253+1522C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238125 | ||||||
| chr9:78238125
|
C | CA | 16 | a0001c0001t0001g0155a0001c0001t0006g0145a0001c0001t0069g0146others(13): Show | 17 | HG00673.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.253+1537dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78238125 | |||||
| chr9:78238137
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0173 | 2 | NA18961.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.253+1534A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238137 | ||||||
| chr9:78238218
|
T | C | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+1615T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238218 | ||||||
| chr9:78238258
|
G | A | 2 | a0001c0003t0027g0208a0001c0003t0056g0202 | 2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.253+1655G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238258 | ||||||
| chr9:78238308
|
G | A | 1 | a0001c0001t0003g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.253+1705G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238308 | ||||||
| chr9:78238405
|
G | A | 1 | a0001c0001t0036g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.254-1618G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238405 | ||||||
| chr9:78238406
|
A | G | 1 | a0001c0001t0036g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.254-1617A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238406 | ||||||
| chr9:78238537
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.254-1486G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238537 | ||||||
| chr9:78238594
|
C | G | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.254-1429C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238594 | ||||||
| chr9:78238596
|
TGTC | T | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-1424_254-1422d others(5): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78238596 | |||||
| chr9:78238718
|
A | T | 73 | a0001c0001t0074g0144a0001c0002t0002g0002a0001c0002t0002g0010others(70): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.254-1305A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238718 | ||||||
| chr9:78238825
|
G | A | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.254-1198G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238825 | ||||||
| chr9:78238970
|
C | T | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.254-1053C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238970 | ||||||
| chr9:78238985
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0121a0001c0001t0072g0013 | 4 | HG02074.hp1 HG02523.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-1038T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78238985 | ||||||
| chr9:78239021
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.254-1002G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239021 | ||||||
| chr9:78239022
|
G | C | 4 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0040g0006others(1): Show | 6 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-1001G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239022 | ||||||
| chr9:78239097
|
C | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.254-926C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239097 | ||||||
| chr9:78239170
|
T | C | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.254-853T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239170 | ||||||
| chr9:78239308
|
A | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.254-715A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239308 | ||||||
| chr9:78239343
|
C | T | 1 | a0001c0001t0067g0199 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.254-680C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239343 | ||||||
| chr9:78239363
|
C | T | 7 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.254-660C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239363 | ||||||
| chr9:78239402
|
C | T | 1 | a0001c0001t0065g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.254-621C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239402 | ||||||
| chr9:78239428
|
T | G | 8 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0035g0098others(5): Show | 10 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-595T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239428 | ||||||
| chr9:78239492
|
T | A | 1 | a0001c0002t0059g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.254-531T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239492 | ||||||
| chr9:78239506
|
A | G | 1 | a0001c0002t0083g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.254-517A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239506 | ||||||
| chr9:78239585
|
G | A | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.254-438G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239585 | ||||||
| chr9:78239595
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.254-428A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239595 | ||||||
| chr9:78239623
|
CTT | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0008g0007 | 6 | HG00140.hp1 HG00735.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-398_254-397del others(2): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 78239623 | |||||
| chr9:78239651
|
C | T | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254-372C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239651 | ||||||
| chr9:78239692
|
G | A | 72 | a0001c0002t0002g0002a0001c0002t0002g0010a0001c0002t0002g0011others(69): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.254-331G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239692 | ||||||
| chr9:78239741
|
G | A | 1 | a0001c0001t0075g0178 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.254-282G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239741 | ||||||
| chr9:78239832
|
A | C | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254-191A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239832 | ||||||
| chr9:78239992
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.254-31A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 1/16 | chr9 | 78239992 | ||||||
| chr9:78240273
|
C | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.427-19C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 2/16 | chr9 | 78240273 | ||||||
| chr9:78240861
|
G | A | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.499+497G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78240861 | ||||||
| chr9:78241005
|
T | G | 1 | a0001c0003t0047g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.499+641T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241005 | ||||||
| chr9:78241050
|
A | G | 1 | a0001c0003t0047g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.500-646A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241050 | ||||||
| chr9:78241094
|
C | CT | 5 | a0001c0001t0003g0018a0001c0001t0003g0227a0001c0001t0003g0228others(2): Show | 7 | HG00673.hp1 HG02083.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.500-600dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 78241094 | |||||
| chr9:78241112
|
G | T | 1 | a0001c0001t0007g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.500-584G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241112 | ||||||
| chr9:78241145
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.500-551C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241145 | ||||||
| chr9:78241239
|
A | G | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.500-457A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241239 | ||||||
| chr9:78241502
|
C | G | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-194C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241502 | ||||||
| chr9:78241529
|
T | G | 1 | a0001c0001t0003g0033 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.500-167T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241529 | ||||||
| chr9:78241539
|
T | G | 73 | a0001c0001t0074g0144a0001c0002t0002g0002a0001c0002t0002g0010others(70): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.500-157T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | chr9 | 78241539 | ||||||
| chr9:78241677
|
G | GT | 13 | a0001c0001t0001g0118a0001c0001t0001g0152a0001c0001t0001g0186others(10): Show | 14 | HG00642.hp2 HG01175.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-10dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 78241677 | |||||
| chr9:78241825
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.603+26A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78241825 | ||||||
| chr9:78241854
|
A | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.603+55A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78241854 | ||||||
| chr9:78241964
|
T | TA | 5 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0142others(2): Show | 5 | HG01081.hp1 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+166dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 78241964 | |||||
| chr9:78241966
|
T | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.603+167T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78241966 | ||||||
| chr9:78241993
|
A | G | 61 | a0001c0002t0002g0002a0001c0002t0002g0010a0001c0002t0002g0011others(58): Show | 72 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.603+194A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78241993 | ||||||
| chr9:78242036
|
A | G | 85 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(82): Show | 97 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.603+237A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242036 | ||||||
| chr9:78242184
|
G | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.603+385G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242184 | ||||||
| chr9:78242200
|
A | T | 1 | a0001c0001t0008g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.603+401A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242200 | ||||||
| chr9:78242255
|
T | C | 27 | a0001c0001t0003g0018a0001c0001t0003g0092a0001c0001t0003g0093others(24): Show | 30 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.603+456T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242255 | ||||||
| chr9:78242391
|
T | G | 162 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(159): Show | 191 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.603+592T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242391 | ||||||
| chr9:78242415
|
G | A | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.603+616G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242415 | ||||||
| chr9:78242430
|
C | T | 72 | a0001c0002t0002g0002a0001c0002t0002g0010a0001c0002t0002g0011others(69): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.603+631C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242430 | ||||||
| chr9:78242638
|
T | C | 1 | a0001c0010t0008g0157 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.604-824T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242638 | ||||||
| chr9:78242752
|
C | T | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.604-710C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242752 | ||||||
| chr9:78242767
|
T | G | 5 | a0001c0002t0002g0037a0001c0002t0002g0053a0001c0002t0002g0054others(2): Show | 5 | HG00438.hp1 NA18948.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-695T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242767 | ||||||
| chr9:78242811
|
T | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.604-651T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242811 | ||||||
| chr9:78242851
|
G | A | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.604-611G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242851 | ||||||
| chr9:78242944
|
A | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.604-518A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242944 | ||||||
| chr9:78242994
|
T | C | 1 | a0001c0001t0087g0102 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.604-468T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78242994 | ||||||
| chr9:78243120
|
T | A | 2 | a0001c0002t0025g0042a0001c0002t0025g0055 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.604-342T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78243120 | ||||||
| chr9:78243126
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.604-336G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78243126 | ||||||
| chr9:78243294
|
A | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.604-168A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78243294 | ||||||
| chr9:78243456
|
T | G | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.604-6T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 4/16 | chr9 | 78243456 | ||||||
| chr9:78243771
|
A | G | 1 | a0001c0002t0002g0050 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.778+135A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78243771 | ||||||
| chr9:78243819
|
C | CA | 72 | a0001c0001t0074g0144a0001c0002t0002g0002a0001c0002t0002g0010others(69): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.778+196dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 78243819 | |||||
| chr9:78243819
|
CA | C | 43 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(40): Show | 49 | HG00323.hp2 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.778+196delA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 78243819 | |||||
| chr9:78244018
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.778+382G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244018 | ||||||
| chr9:78244134
|
C | CT | 19 | a0001c0001t0008g0194a0001c0001t0011g0104a0001c0001t0012g0017others(16): Show | 22 | HG00738.hp2 HG01071.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.778+521dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 78244134 | |||||
| chr9:78244134
|
CT | C | 14 | a0001c0001t0001g0158a0001c0001t0064g0153a0001c0002t0002g0056others(11): Show | 15 | HG00544.hp1 HG01070.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.778+521delT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 78244134 | |||||
| chr9:78244134
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0029a0001c0001t0001g0198a0001c0001t0001g0200others(2): Show | 6 | HG01123.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+512_778+521del others(10): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 78244134 | |||||
| chr9:78244176
|
G | A | 1 | a0001c0001t0015g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.778+540G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244176 | ||||||
| chr9:78244316
|
C | T | 3 | a0001c0001t0007g0125a0001c0001t0007g0142a0002c0011t0007g0126 | 3 | HG02895.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.778+680C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244316 | ||||||
| chr9:78244534
|
G | A | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.778+898G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244534 | ||||||
| chr9:78244622
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.778+986T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244622 | ||||||
| chr9:78244674
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.778+1038A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244674 | ||||||
| chr9:78244842
|
G | T | 1 | a0001c0002t0052g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.778+1206G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244842 | ||||||
| chr9:78244944
|
G | A | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.778+1308G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78244944 | ||||||
| chr9:78245053
|
C | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.778+1417C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245053 | ||||||
| chr9:78245244
|
G | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.779-1425G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245244 | ||||||
| chr9:78245246
|
G | A | 2 | a0001c0003t0027g0208a0001c0003t0056g0202 | 2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.779-1423G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245246 | ||||||
| chr9:78245289
|
C | A | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.779-1380C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245289 | ||||||
| chr9:78245335
|
G | A | 1 | a0001c0001t0013g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.779-1334G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245335 | ||||||
| chr9:78245470
|
C | G | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.779-1199C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245470 | ||||||
| chr9:78245638
|
A | G | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.779-1031A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245638 | ||||||
| chr9:78245642
|
C | T | 33 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(30): Show | 37 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.779-1027C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245642 | ||||||
| chr9:78245980
|
A | G | 1 | a0001c0002t0002g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.779-689A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78245980 | ||||||
| chr9:78246022
|
G | A | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.779-647G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246022 | ||||||
| chr9:78246225
|
C | T | 23 | a0001c0003t0004g0016a0001c0003t0004g0031a0001c0003t0004g0176others(20): Show | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.779-444C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246225 | ||||||
| chr9:78246243
|
A | G | 1 | a0001c0001t0060g0105 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.779-426A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246243 | ||||||
| chr9:78246344
|
A | G | 8 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0035g0098others(5): Show | 10 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.779-325A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246344 | ||||||
| chr9:78246368
|
G | A | 2 | a0001c0001t0003g0229a0001c0001t0015g0230 | 2 | HG02129.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.779-301G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246368 | ||||||
| chr9:78246473
|
G | A | 1 | a0001c0001t0003g0239 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.779-196G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246473 | ||||||
| chr9:78246601
|
A | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.779-68A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 5/16 | chr9 | 78246601 | ||||||
| chr9:78246849
|
A | G | 2 | a0001c0002t0002g0065a0001c0002t0002g0087 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.892+67A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78246849 | ||||||
| chr9:78246863
|
T | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.892+81T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78246863 | ||||||
| chr9:78247023
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.892+241A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247023 | ||||||
| chr9:78247086
|
G | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.892+304G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247086 | ||||||
| chr9:78247105
|
C | T | 9 | a0001c0002t0005g0005a0001c0002t0005g0067a0001c0002t0005g0068others(6): Show | 12 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.892+323C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247105 | ||||||
| chr9:78247315
|
G | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.892+533G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247315 | ||||||
| chr9:78247471
|
G | A | 4 | a0001c0004t0023g0213a0001c0004t0046g0221a0001c0004t0054g0119others(1): Show | 4 | HG01255.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+689G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247471 | ||||||
| chr9:78247525
|
C | T | 1 | a0001c0002t0052g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.892+743C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247525 | ||||||
| chr9:78247529
|
G | A | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.892+747G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247529 | ||||||
| chr9:78247540
|
G | A | 7 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.893-751G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247540 | ||||||
| chr9:78247768
|
G | A | 1 | a0001c0003t0004g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.893-523G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247768 | ||||||
| chr9:78247919
|
C | T | 1 | a0001c0003t0048g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.893-372C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247919 | ||||||
| chr9:78247942
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.893-349G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247942 | ||||||
| chr9:78247959
|
T | A | 1 | a0001c0003t0088g0174 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.893-332T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247959 | ||||||
| chr9:78247999
|
T | A | 7 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0142others(4): Show | 8 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.893-292T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78247999 | ||||||
| chr9:78248092
|
C | A | 5 | a0001c0001t0011g0104a0001c0001t0087g0102a0001c0005t0011g0008others(2): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-199C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78248092 | ||||||
| chr9:78248156
|
T | C | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.893-135T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78248156 | ||||||
| chr9:78248172
|
G | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(208): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.893-119G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78248172 | ||||||
| chr9:78248206
|
A | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.893-85A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 6/16 | chr9 | 78248206 | ||||||
| chr9:78248417
|
C | T | 1 | a0001c0001t0010g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.957+62C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 7/16 | chr9 | 78248417 | ||||||
| chr9:78248515
|
G | T | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.957+160G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 7/16 | chr9 | 78248515 | ||||||
| chr9:78248620
|
G | A | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.958-142G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 7/16 | chr9 | 78248620 | ||||||
| chr9:78248634
|
T | C | 5 | a0001c0001t0011g0104a0001c0001t0087g0102a0001c0005t0011g0008others(2): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-128T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 7/16 | chr9 | 78248634 | ||||||
| chr9:78248981
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1069+108G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78248981 | ||||||
| chr9:78249069
|
T | C | 33 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(30): Show | 37 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1069+196T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249069 | ||||||
| chr9:78249171
|
A | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069+298A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249171 | ||||||
| chr9:78249193
|
G | T | 33 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(30): Show | 37 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1069+320G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249193 | ||||||
| chr9:78249224
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1069+351T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249224 | ||||||
| chr9:78249224
|
T | TTTGTCGT others(2): Show |
11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1069+355_1069+356i others(11): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 78249224 | |||||
| chr9:78249224
|
T | TTTGTTGT others(2): Show |
145 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(142): Show | 170 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1069+359_1069+360i others(11): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 78249224 | |||||
| chr9:78249596
|
T | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(235): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1069+723T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249596 | ||||||
| chr9:78249625
|
T | C | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1069+752T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249625 | ||||||
| chr9:78249702
|
A | G | 4 | a0001c0004t0023g0213a0001c0004t0046g0221a0001c0004t0054g0119others(1): Show | 4 | HG01255.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+829A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249702 | ||||||
| chr9:78249947
|
C | A | 6 | a0001c0001t0038g0251a0001c0002t0002g0010a0001c0002t0002g0056others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+1074C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78249947 | ||||||
| chr9:78250100
|
T | C | 1 | a0001c0002t0005g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1069+1227T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250100 | ||||||
| chr9:78250414
|
A | C | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-1494A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250414 | ||||||
| chr9:78250596
|
G | A | 1 | a0001c0001t0084g0160 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1070-1312G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250596 | ||||||
| chr9:78250770
|
C | T | 4 | a0001c0004t0023g0213a0001c0004t0046g0221a0001c0004t0054g0119others(1): Show | 4 | HG01255.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-1138C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250770 | ||||||
| chr9:78250867
|
G | A | 55 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(52): Show | 62 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1070-1041G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250867 | ||||||
| chr9:78250869
|
A | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1070-1039A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250869 | ||||||
| chr9:78250889
|
T | G | 7 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0142others(4): Show | 8 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-1019T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250889 | ||||||
| chr9:78250899
|
A | G | 163 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(160): Show | 192 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1070-1009A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250899 | ||||||
| chr9:78250927
|
A | G | 2 | a0001c0004t0014g0030a0001c0004t0080g0030 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1070-981A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250927 | ||||||
| chr9:78250978
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1070-930C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78250978 | ||||||
| chr9:78251037
|
G | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1070-871G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251037 | ||||||
| chr9:78251292
|
A | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0001t0001g0184others(4): Show | 8 | HG01123.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-616A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251292 | ||||||
| chr9:78251391
|
C | G | 2 | a0001c0001t0038g0251a0001c0009t0091g0201 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1070-517C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251391 | ||||||
| chr9:78251599
|
T | A | 1 | a0001c0001t0078g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1070-309T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251599 | ||||||
| chr9:78251610
|
G | A | 1 | a0001c0004t0028g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1070-298G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251610 | ||||||
| chr9:78251734
|
T | C | 73 | a0001c0001t0074g0144a0001c0002t0002g0002a0001c0002t0002g0010others(70): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1070-174T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251734 | ||||||
| chr9:78251830
|
A | C | 1 | a0001c0001t0082g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1070-78A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 8/16 | chr9 | 78251830 | ||||||
| chr9:78252084
|
G | C | 1 | a0003c0008t0073g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1205+41G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252084 | ||||||
| chr9:78252225
|
A | G | 1 | a0001c0003t0009g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1205+182A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252225 | ||||||
| chr9:78252452
|
T | G | 23 | a0001c0003t0004g0016a0001c0003t0004g0031a0001c0003t0004g0176others(20): Show | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1205+409T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252452 | ||||||
| chr9:78252464
|
C | G | 1 | a0001c0002t0002g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1205+421C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252464 | ||||||
| chr9:78252495
|
GATATAAC | G | 3 | a0001c0001t0015g0225a0001c0001t0015g0242a0001c0001t0092g0236 | 3 | HG00323.hp2 HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1205+453_1205+459d others(9): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252495 | ||||||
| chr9:78252600
|
G | C | 1 | a0001c0002t0002g0079 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1205+557G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252600 | ||||||
| chr9:78252620
|
A | C | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1205+577A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252620 | ||||||
| chr9:78252673
|
T | G | 3 | a0001c0001t0015g0225a0001c0001t0015g0242a0001c0001t0092g0236 | 3 | HG00323.hp2 HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1206-559T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252673 | ||||||
| chr9:78252675
|
A | G | 73 | a0001c0001t0074g0144a0001c0002t0002g0002a0001c0002t0002g0010others(70): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1206-557A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252675 | ||||||
| chr9:78252988
|
G | A | 3 | a0001c0002t0002g0037a0001c0002t0002g0054a0001c0002t0022g0052 | 3 | HG00438.hp1 NA18948.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1206-244G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78252988 | ||||||
| chr9:78253115
|
T | C | 7 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1206-117T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78253115 | ||||||
| chr9:78253185
|
G | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1206-47G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 9/16 | chr9 | 78253185 | ||||||
| chr9:78253406
|
A | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1251+129A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78253406 | ||||||
| chr9:78253438
|
G | T | 163 | a0001c0001t0001g0121a0001c0001t0003g0018a0001c0001t0003g0033others(160): Show | 192 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1251+161G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78253438 | ||||||
| chr9:78253858
|
T | G | 3 | a0001c0001t0015g0225a0001c0001t0015g0242a0001c0001t0092g0236 | 3 | HG00323.hp2 HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1251+581T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78253858 | ||||||
| chr9:78253891
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251+614G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78253891 | ||||||
| chr9:78253943
|
G | A | 5 | a0001c0002t0002g0043a0001c0002t0002g0058a0001c0002t0002g0072others(2): Show | 5 | HG01099.hp1 HG01192.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251+666G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78253943 | ||||||
| chr9:78253965
|
A | G | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1251+688A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78253965 | ||||||
| chr9:78254084
|
C | T | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1252-752C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254084 | ||||||
| chr9:78254171
|
G | T | 1 | a0001c0003t0009g0218 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1252-665G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254171 | ||||||
| chr9:78254268
|
A | G | 1 | a0001c0003t0004g0212 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1252-568A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254268 | ||||||
| chr9:78254291
|
C | A | 1 | a0001c0002t0002g0020 | 2 | HG00733.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1252-545C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254291 | ||||||
| chr9:78254350
|
T | G | 8 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0035g0098others(5): Show | 10 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1252-486T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254350 | ||||||
| chr9:78254436
|
C | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1252-400C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254436 | ||||||
| chr9:78254451
|
C | CTG | 7 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1252-378_1252-377d others(4): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 78254451 | |||||
| chr9:78254489
|
T | C | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1252-347T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254489 | ||||||
| chr9:78254522
|
T | C | 4 | a0001c0001t0038g0251a0001c0001t0064g0153a0001c0001t0096g0123others(1): Show | 4 | HG01070.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1252-314T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254522 | ||||||
| chr9:78254610
|
G | A | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1252-226G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254610 | ||||||
| chr9:78254666
|
GAATAA | G | 5 | a0001c0004t0014g0023a0001c0004t0014g0115a0001c0004t0028g0219others(2): Show | 6 | HG02572.hp2 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1252-169_1252-165d others(7): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 10/16 | chr9 | 78254666 | ||||||
| chr9:78255006
|
A | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1380+42A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78255006 | ||||||
| chr9:78255516
|
C | T | 16 | a0001c0001t0003g0018a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 18 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1380+552C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78255516 | ||||||
| chr9:78255769
|
T | A | 157 | a0001c0001t0001g0121a0001c0001t0003g0018a0001c0001t0003g0033others(154): Show | 183 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1380+805T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78255769 | ||||||
| chr9:78255870
|
T | G | 1 | a0001c0001t0035g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1380+906T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78255870 | ||||||
| chr9:78256103
|
A | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1380+1139A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256103 | ||||||
| chr9:78256162
|
C | T | 1 | a0002c0011t0007g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1380+1198C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256162 | ||||||
| chr9:78256448
|
C | A | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1380+1484C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256448 | ||||||
| chr9:78256524
|
A | AT | 22 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0150others(19): Show | 25 | HG01891.hp1 HG02004.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.1380+1586dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78256524 | |||||
| chr9:78256524
|
AT | A | 127 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0001g0171others(124): Show | 152 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1380+1586delT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78256524 | |||||
| chr9:78256524
|
ATT | A | 17 | a0001c0001t0003g0227a0001c0001t0012g0237a0001c0001t0016g0247others(14): Show | 18 | HG01069.hp2 HG01070.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1380+1585_1380+158 others(6): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78256524 | |||||
| chr9:78256534
|
T | A | 7 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0142others(4): Show | 8 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1380+1570T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256534 | ||||||
| chr9:78256540
|
T | A | 1 | a0002c0011t0007g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1380+1576T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256540 | ||||||
| chr9:78256541
|
T | A | 2 | a0001c0001t0020g0024a0001c0001t0020g0148 | 3 | HG01168.hp2 HG01169.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1380+1577T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256541 | ||||||
| chr9:78256580
|
T | A | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1380+1616T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256580 | ||||||
| chr9:78256623
|
T | C | 3 | a0001c0001t0038g0251a0001c0001t0096g0123a0001c0009t0091g0201 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1380+1659T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256623 | ||||||
| chr9:78256634
|
G | A | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380+1670G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256634 | ||||||
| chr9:78256717
|
C | T | 1 | a0001c0001t0019g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1380+1753C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256717 | ||||||
| chr9:78256796
|
A | G | 1 | a0001c0002t0081g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1380+1832A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256796 | ||||||
| chr9:78256805
|
A | G | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1380+1841A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256805 | ||||||
| chr9:78256882
|
G | A | 4 | a0001c0002t0002g0059a0001c0002t0002g0071a0001c0002t0025g0042others(1): Show | 4 | HG01074.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+1918G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256882 | ||||||
| chr9:78256933
|
A | G | 2 | a0001c0001t0096g0123a0001c0009t0091g0201 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1380+1969A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256933 | ||||||
| chr9:78256980
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0019g0028others(1): Show | 4 | HG00323.hp1 HG01346.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+2016A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78256980 | ||||||
| chr9:78257087
|
A | G | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+2123A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257087 | ||||||
| chr9:78257105
|
C | CA | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380+2152dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78257105 | |||||
| chr9:78257218
|
C | T | 4 | a0001c0001t0017g0009a0001c0001t0017g0101a0001c0001t0029g0009others(1): Show | 6 | HG01891.hp2 HG02486.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380+2254C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257218 | ||||||
| chr9:78257361
|
G | T | 7 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(4): Show | 8 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1380+2397G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257361 | ||||||
| chr9:78257364
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1380+2400G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257364 | ||||||
| chr9:78257392
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0010g0188a0001c0001t0068g0185 | 3 | NA18949.hp2 NA18960.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1380+2428C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257392 | ||||||
| chr9:78257428
|
C | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1380+2464C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257428 | ||||||
| chr9:78257476
|
A | T | 1 | a0001c0001t0041g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1380+2512A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257476 | ||||||
| chr9:78257629
|
A | G | 2 | a0001c0002t0002g0065a0001c0002t0002g0087 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1380+2665A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257629 | ||||||
| chr9:78257880
|
G | C | 1 | a0001c0003t0048g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1380+2916G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257880 | ||||||
| chr9:78257947
|
C | T | 1 | a0001c0002t0002g0086 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1380+2983C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257947 | ||||||
| chr9:78257992
|
T | G | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380+3028T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78257992 | ||||||
| chr9:78258055
|
A | C | 1 | a0001c0001t0003g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1380+3091A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258055 | ||||||
| chr9:78258403
|
G | A | 1 | a0001c0001t0007g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1380+3439G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258403 | ||||||
| chr9:78258908
|
G | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0128others(5): Show | 16 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.1380+3944G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258908 | ||||||
| chr9:78258909
|
A | C | 1 | a0001c0002t0026g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1380+3945A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258909 | ||||||
| chr9:78258926
|
C | T | 4 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0040g0006others(1): Show | 6 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1380+3962C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258926 | ||||||
| chr9:78258940
|
C | T | 1 | a0001c0007t0063g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1381-3967C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258940 | ||||||
| chr9:78258968
|
A | G | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1381-3939A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78258968 | ||||||
| chr9:78259041
|
G | A | 1 | a0001c0002t0002g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1381-3866G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259041 | ||||||
| chr9:78259138
|
A | G | 1 | a0001c0002t0002g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1381-3769A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259138 | ||||||
| chr9:78259260
|
C | T | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1381-3647C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259260 | ||||||
| chr9:78259407
|
A | G | 12 | a0001c0001t0007g0124a0001c0001t0007g0125a0001c0001t0007g0142others(9): Show | 16 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1381-3500A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259407 | ||||||
| chr9:78259422
|
T | C | 163 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(160): Show | 192 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1381-3485T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259422 | ||||||
| chr9:78259459
|
T | A | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-3448T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259459 | ||||||
| chr9:78259470
|
A | G | 2 | a0001c0002t0007g0051a0001c0002t0024g0077 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1381-3437A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259470 | ||||||
| chr9:78259591
|
A | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1381-3316A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259591 | ||||||
| chr9:78259800
|
A | G | 5 | a0001c0001t0011g0104a0001c0001t0087g0102a0001c0005t0011g0008others(2): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-3107A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78259800 | ||||||
| chr9:78260093
|
T | C | 9 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(6): Show | 10 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1381-2814T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260093 | ||||||
| chr9:78260306
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1381-2601A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260306 | ||||||
| chr9:78260322
|
T | C | 1 | a0001c0001t0078g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1381-2585T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260322 | ||||||
| chr9:78260324
|
G | GA | 9 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(6): Show | 10 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1381-2580dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78260324 | |||||
| chr9:78260433
|
T | C | 9 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(6): Show | 10 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1381-2474T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260433 | ||||||
| chr9:78260551
|
C | T | 1 | a0001c0003t0009g0032 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1381-2356C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260551 | ||||||
| chr9:78260634
|
G | T | 2 | a0001c0002t0007g0051a0001c0002t0024g0077 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1381-2273G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260634 | ||||||
| chr9:78260706
|
C | CA | 21 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0193others(18): Show | 25 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1381-2182dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78260706 | |||||
| chr9:78260876
|
C | G | 2 | a0001c0004t0014g0030a0001c0004t0080g0030 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1381-2031C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78260876 | ||||||
| chr9:78260949
|
TTTTG | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0180a0001c0001t0001g0198others(2): Show | 6 | HG01123.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381-1942_1381-193 others(8): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78260949 | |||||
| chr9:78261097
|
C | T | 1 | a0001c0001t0035g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1381-1810C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261097 | ||||||
| chr9:78261098
|
G | A | 1 | a0001c0003t0004g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1381-1809G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261098 | ||||||
| chr9:78261157
|
G | A | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-1750G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261157 | ||||||
| chr9:78261191
|
C | T | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1381-1716C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261191 | ||||||
| chr9:78261323
|
G | A | 3 | a0001c0001t0038g0251a0001c0001t0096g0123a0001c0009t0091g0201 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1381-1584G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261323 | ||||||
| chr9:78261325
|
G | T | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1381-1582G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261325 | ||||||
| chr9:78261775
|
T | C | 2 | a0001c0004t0014g0023a0001c0004t0014g0115 | 3 | HG02572.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1381-1132T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261775 | ||||||
| chr9:78261910
|
G | A | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1381-997G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261910 | ||||||
| chr9:78261988
|
A | G | 8 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0035g0098others(5): Show | 10 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1381-919A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78261988 | ||||||
| chr9:78262148
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1381-759C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262148 | ||||||
| chr9:78262151
|
A | G | 1 | a0001c0001t0086g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1381-756A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262151 | ||||||
| chr9:78262202
|
A | AT | 47 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0003g0018others(44): Show | 53 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1381-688dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 78262202 | |||||
| chr9:78262204
|
T | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1381-703T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262204 | ||||||
| chr9:78262337
|
G | A | 2 | a0001c0003t0004g0204a0001c0003t0004g0211 | 2 | NA18966.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1381-570G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262337 | ||||||
| chr9:78262343
|
A | G | 23 | a0001c0003t0004g0016a0001c0003t0004g0031a0001c0003t0004g0176others(20): Show | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1381-564A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262343 | ||||||
| chr9:78262535
|
C | A | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1381-372C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262535 | ||||||
| chr9:78262762
|
A | G | 1 | a0001c0002t0002g0086 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1381-145A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262762 | ||||||
| chr9:78262825
|
C | T | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1381-82C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262825 | ||||||
| chr9:78262861
|
C | T | 73 | a0001c0001t0074g0144a0001c0002t0002g0002a0001c0002t0002g0010others(70): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1381-46C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 11/16 | chr9 | 78262861 | ||||||
| chr9:78263092
|
G | C | 4 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0040g0006others(1): Show | 6 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1458+108G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78263092 | ||||||
| chr9:78263126
|
A | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0171a0001c0001t0031g0112others(1): Show | 4 | HG02735.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1458+142A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78263126 | ||||||
| chr9:78263134
|
A | G | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1458+150A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78263134 | ||||||
| chr9:78263463
|
A | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0197 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1458+479A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78263463 | ||||||
| chr9:78263593
|
G | T | 7 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1459-557G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78263593 | ||||||
| chr9:78263992
|
T | C | 2 | a0001c0001t0096g0123a0001c0009t0091g0201 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1459-158T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78263992 | ||||||
| chr9:78264054
|
A | T | 1 | a0001c0001t0016g0232 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1459-96A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78264054 | ||||||
| chr9:78264089
|
A | T | 4 | a0001c0002t0002g0020a0001c0002t0002g0062a0001c0002t0002g0069others(1): Show | 5 | HG00733.hp2 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1459-61A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78264089 | ||||||
| chr9:78264103
|
G | A | 5 | a0001c0004t0014g0023a0001c0004t0014g0115a0001c0004t0028g0219others(2): Show | 6 | HG02572.hp2 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1459-47G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 12/16 | chr9 | 78264103 | ||||||
| chr9:78264364
|
G | A | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1625+48G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78264364 | ||||||
| chr9:78264384
|
A | G | 1 | a0001c0002t0002g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1625+68A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78264384 | ||||||
| chr9:78264645
|
T | TA | 39 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(36): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1625+349dupA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 78264645 | |||||
| chr9:78264645
|
TA | T | 24 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0003g0093others(21): Show | 26 | HG00558.hp1 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1625+349delA | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 78264645 | |||||
| chr9:78264645
|
TAA | T | 18 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(15): Show | 23 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1625+348_1625+349d others(4): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 78264645 | |||||
| chr9:78264699
|
G | A | 7 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(4): Show | 8 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1625+383G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78264699 | ||||||
| chr9:78264923
|
T | A | 1 | a0001c0002t0005g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1626-449T>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78264923 | ||||||
| chr9:78264970
|
G | T | 7 | a0001c0001t0003g0018a0001c0001t0003g0092a0001c0001t0003g0093others(4): Show | 9 | HG00673.hp1 HG02083.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-402G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78264970 | ||||||
| chr9:78264973
|
G | A | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626-399G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78264973 | ||||||
| chr9:78265083
|
AC | A | 72 | a0001c0002t0002g0002a0001c0002t0002g0010a0001c0002t0002g0011others(69): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1626-288delC | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78265083 | ||||||
| chr9:78265351
|
T | G | 4 | a0001c0001t0017g0009a0001c0001t0017g0101a0001c0001t0029g0009others(1): Show | 6 | HG01891.hp2 HG02486.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626-21T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 13/16 | chr9 | 78265351 | ||||||
| chr9:78265557
|
A | G | 1 | a0001c0001t0093g0234 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1797+14A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/16 | chr9 | 78265557 | ||||||
| chr9:78265560
|
G | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1797+17G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/16 | chr9 | 78265560 | ||||||
| chr9:78265619
|
G | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1797+76G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/16 | chr9 | 78265619 | ||||||
| chr9:78265640
|
C | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1797+97C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/16 | chr9 | 78265640 | ||||||
| chr9:78265642
|
C | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1797+99C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/16 | chr9 | 78265642 | ||||||
| chr9:78265755
|
TTA | T | 4 | a0001c0004t0023g0213a0001c0004t0046g0221a0001c0004t0054g0119others(1): Show | 4 | HG01255.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1798-102_1798-101d others(4): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr9 | 78265755 | |||||
| chr9:78265951
|
A | C | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1845+45A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 15/16 | chr9 | 78265951 | ||||||
| chr9:78265976
|
A | ATC | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1845+71_1845+72dup others(2): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 78265976 | |||||
| chr9:78266124
|
A | G | 1 | a0001c0001t0077g0117 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1845+218A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 15/16 | chr9 | 78266124 | ||||||
| chr9:78266176
|
A | T | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1846-266A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 15/16 | chr9 | 78266176 | ||||||
| chr9:78266372
|
C | T | 7 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1846-70C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 15/16 | chr9 | 78266372 | ||||||
| chr9:78266383
|
C | G | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1846-59C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 15/16 | chr9 | 78266383 | ||||||
| chr9:78266806
|
C | G | 1 | a0001c0001t0082g0137 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2107+103C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78266806 | ||||||
| chr9:78266813
|
T | C | 3 | a0001c0001t0006g0027a0001c0001t0006g0145a0001c0001t0006g0151 | 4 | NA18970.hp2 NA18999.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+110T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78266813 | ||||||
| chr9:78266855
|
C | T | 10 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(7): Show | 12 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.2107+152C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78266855 | ||||||
| chr9:78267350
|
G | A | 1 | a0001c0002t0002g0057 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2107+647G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267350 | ||||||
| chr9:78267701
|
A | G | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2107+998A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267701 | ||||||
| chr9:78267781
|
G | A | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2107+1078G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267781 | ||||||
| chr9:78267814
|
C | T | 1 | a0001c0002t0044g0089 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2107+1111C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267814 | ||||||
| chr9:78267832
|
A | G | 1 | a0001c0001t0090g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2107+1129A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267832 | ||||||
| chr9:78267840
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2107+1137C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267840 | ||||||
| chr9:78267940
|
C | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2107+1237C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78267940 | ||||||
| chr9:78268065
|
C | T | 11 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(8): Show | 12 | HG01255.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2107+1362C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268065 | ||||||
| chr9:78268158
|
A | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2107+1455A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268158 | ||||||
| chr9:78268327
|
T | C | 1 | a0001c0001t0077g0117 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2107+1624T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268327 | ||||||
| chr9:78268332
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0140a0001c0001t0006g0141others(3): Show | 7 | NA18950.hp1 NA18953.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+1629G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268332 | ||||||
| chr9:78268377
|
G | A | 23 | a0001c0003t0004g0016a0001c0003t0004g0031a0001c0003t0004g0176others(20): Show | 27 | HG00408.hp2 HG01069.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2107+1674G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268377 | ||||||
| chr9:78268400
|
G | A | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2107+1697G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268400 | ||||||
| chr9:78268610
|
C | T | 1 | a0001c0003t0048g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2107+1907C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268610 | ||||||
| chr9:78268629
|
G | T | 7 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2107+1926G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268629 | ||||||
| chr9:78268642
|
G | A | 1 | a0001c0003t0061g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2107+1939G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268642 | ||||||
| chr9:78268658
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0155a0001c0001t0036g0147 | 4 | HG00544.hp2 HG03927.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+1955T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268658 | ||||||
| chr9:78268672
|
T | C | 1 | a0001c0003t0061g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2107+1969T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268672 | ||||||
| chr9:78268680
|
C | CT | 7 | a0001c0001t0001g0135a0001c0001t0001g0163a0001c0001t0001g0173others(4): Show | 7 | HG02258.hp2 HG02615.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+1997dupT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 78268680 | |||||
| chr9:78268680
|
C | CTT | 6 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0039g0107others(3): Show | 8 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2107+1996_2107+199 others(6): Show |
CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 78268680 | |||||
| chr9:78268680
|
CT | C | 12 | a0001c0001t0001g0171a0001c0001t0001g0187a0001c0001t0007g0125others(9): Show | 13 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2107+1997delT | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 78268680 | |||||
| chr9:78268684
|
T | C | 2 | a0001c0003t0009g0032a0001c0009t0091g0201 | 3 | HG02717.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2107+1981T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268684 | ||||||
| chr9:78268685
|
T | C | 75 | a0001c0001t0030g0133a0001c0001t0030g0149a0001c0001t0074g0144others(72): Show | 89 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2107+1982T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268685 | ||||||
| chr9:78268687
|
T | C | 1 | a0001c0001t0064g0153 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2107+1984T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268687 | ||||||
| chr9:78268690
|
T | C | 1 | a0001c0002t0051g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2107+1987T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268690 | ||||||
| chr9:78268797
|
G | C | 28 | a0001c0001t0013g0006a0001c0001t0013g0106a0001c0001t0021g0012others(25): Show | 32 | HG00642.hp2 HG01255.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.2108-2044G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268797 | ||||||
| chr9:78268846
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0128others(5): Show | 16 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2108-1995C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268846 | ||||||
| chr9:78268858
|
G | A | 27 | a0001c0001t0003g0018a0001c0001t0003g0092a0001c0001t0003g0093others(24): Show | 30 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.2108-1983G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268858 | ||||||
| chr9:78268951
|
T | C | 62 | a0001c0001t0003g0018a0001c0001t0003g0033a0001c0001t0003g0092others(59): Show | 70 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.2108-1890T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268951 | ||||||
| chr9:78268952
|
G | C | 4 | a0001c0004t0023g0213a0001c0004t0046g0221a0001c0004t0054g0119others(1): Show | 4 | HG01255.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108-1889G>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78268952 | ||||||
| chr9:78269009
|
C | G | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2108-1832C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269009 | ||||||
| chr9:78269064
|
T | C | 6 | a0001c0001t0021g0012a0001c0001t0021g0095a0001c0001t0033g0012others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108-1777T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269064 | ||||||
| chr9:78269096
|
C | G | 1 | a0001c0003t0056g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2108-1745C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269096 | ||||||
| chr9:78269277
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2108-1564G>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269277 | ||||||
| chr9:78269772
|
G | A | 1 | a0001c0001t0096g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2108-1069G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269772 | ||||||
| chr9:78269798
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2108-1043G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269798 | ||||||
| chr9:78269860
|
A | G | 4 | a0001c0002t0002g0036a0001c0002t0002g0045a0001c0002t0002g0047others(1): Show | 4 | HG02027.hp1 NA18952.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108-981A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269860 | ||||||
| chr9:78269893
|
C | G | 7 | a0001c0004t0014g0023a0001c0004t0014g0030a0001c0004t0014g0115others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2108-948C>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269893 | ||||||
| chr9:78269943
|
C | A | 2 | a0001c0001t0035g0098a0001c0001t0035g0099 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2108-898C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269943 | ||||||
| chr9:78269971
|
T | C | 1 | a0001c0001t0078g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2108-870T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78269971 | ||||||
| chr9:78270169
|
A | G | 2 | a0001c0004t0014g0030a0001c0004t0080g0030 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2108-672A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270169 | ||||||
| chr9:78270225
|
A | T | 1 | a0001c0001t0003g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2108-616A>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270225 | ||||||
| chr9:78270227
|
A | G | 2 | a0001c0002t0005g0068a0001c0002t0044g0089 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2108-614A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270227 | ||||||
| chr9:78270336
|
T | C | 4 | a0001c0001t0017g0009a0001c0001t0017g0101a0001c0001t0029g0009others(1): Show | 6 | HG01891.hp2 HG02486.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-505T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270336 | ||||||
| chr9:78270439
|
T | C | 5 | a0001c0001t0011g0104a0001c0001t0087g0102a0001c0005t0011g0008others(2): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2108-402T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270439 | ||||||
| chr9:78270479
|
A | G | 8 | a0001c0001t0012g0017a0001c0001t0012g0226a0001c0001t0012g0231others(5): Show | 9 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108-362A>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270479 | ||||||
| chr9:78270571
|
C | A | 2 | a0001c0003t0004g0016a0001c0003t0004g0214 | 4 | HG00408.hp2 HG02015.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108-270C>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270571 | ||||||
| chr9:78270588
|
T | C | 1 | a0001c0001t0038g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2108-253T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270588 | ||||||
| chr9:78270608
|
T | C | 5 | a0001c0003t0009g0032a0001c0003t0009g0215a0001c0003t0009g0217others(2): Show | 6 | HG01192.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-233T>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270608 | ||||||
| chr9:78270622
|
A | C | 1 | a0001c0009t0091g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-219A>C | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270622 | ||||||
| chr9:78270668
|
G | A | 1 | a0001c0003t0047g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2108-173G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270668 | ||||||
| chr9:78270670
|
T | G | 1 | a0001c0003t0047g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2108-171T>G | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270670 | ||||||
| chr9:78270740
|
C | T | 1 | a0001c0001t0074g0144 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2108-101C>T | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270740 | ||||||
| chr9:78270741
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0186 | 2 | HG01175.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2108-100G>A | CEP78 | ENSG00000148019.14 | transcript | ENST00000643273.2 | protein_coding | 16/16 | chr9 | 78270741 |