Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 143384 |
|---|---|
| ensemblid | ENSG00000151893.15 |
| hgncid | 23727 |
| symbol | CACUL1 |
| name | CDK2 associated cullin domain 1 |
| refseq_nuc | NM_153810.5 |
| refseq_prot | NP_722517.3 |
| ensembl_nuc | ENST00000369151.8 |
| ensembl_prot | ENSP00000358147.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 118676411 |
| end | 118754970 |
| strand | - |
| ver | v1.2 |
| region | chr10:118676411-118754970 |
| region5000 | chr10:118671411-118759970 |
| regionname0 | CACUL1_chr10_118676411_118754970 |
| regionname5000 | CACUL1_chr10_118671411_118759970 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 369 | 387 | 90 | 62 | 178 | 14 | 41 | 144 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0002 | 0/0 | 369 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1110 | 367 | 82 | 56 | 176 | 12 | 39 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| c0002 | 0/0 | 1110 | 16 | 8 | 6 | 1 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| c0003 | 0/0 | 1110 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| c0004 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| c0005 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| c0006 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9921 | 78 | 17 | 11 | 40 | 2 | 8 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0002 | 0/0 | 9925 | 28 | 1 | 7 | 11 | 3 | 6 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0003 | 0/0 | 9932 | 28 | 1 | 5 | 21 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0004 | 0/0 | 9926 | 25 | 3 | 6 | 9 | 2 | 5 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0005 | 1/0 | 9926 | 17 | 11 | 1 | 3 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0006 | 0/0 | 9926 | 15 | 0 | 0 | 13 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0007 | 0/0 | 9927 | 9 | 1 | 2 | 2 | 1 | 3 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0008 | 0/0 | 9936 | 8 | 8 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0009 | 0/0 | 9926 | 7 | 0 | 0 | 7 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0010 | 0/0 | 10011 | 6 | 3 | 2 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0011 | 0/0 | 9932 | 6 | 0 | 0 | 6 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0012 | 0/0 | 9924 | 6 | 2 | 2 | 1 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0013 | 0/0 | 9932 | 6 | 0 | 0 | 6 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0014 | 0/0 | 9933 | 6 | 0 | 3 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0015 | 0/0 | 10010 | 6 | 1 | 4 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0016 | 0/0 | 9928 | 5 | 5 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0017 | 0/0 | 9921 | 5 | 0 | 0 | 5 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0018 | 0/1 | 10010 | 5 | 0 | 1 | 0 | 0 | 3 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0019 | 0/0 | 9920 | 4 | 2 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0020 | 0/0 | 9922 | 4 | 1 | 3 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0021 | 0/0 | 9922 | 4 | 0 | 0 | 4 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0022 | 0/0 | 9926 | 3 | 3 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0023 | 0/0 | 9922 | 3 | 0 | 1 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0024 | 0/0 | 9921 | 3 | 0 | 2 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0025 | 0/0 | 9924 | 3 | 0 | 0 | 0 | 0 | 3 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0026 | 0/0 | 9921 | 3 | 0 | 0 | 2 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0027 | 0/0 | 9932 | 3 | 0 | 0 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0028 | 0/0 | 9926 | 3 | 0 | 1 | 0 | 2 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0029 | 0/0 | 9922 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0030 | 0/0 | 9936 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0031 | 0/0 | 9932 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0032 | 0/0 | 9924 | 2 | 0 | 0 | 1 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0033 | 0/0 | 9930 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0034 | 0/0 | 9920 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0035 | 0/0 | 9926 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0036 | 0/0 | 9927 | 2 | 1 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0037 | 0/0 | 9919 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0038 | 0/0 | 9923 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0039 | 0/0 | 9936 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0040 | 0/0 | 9925 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0041 | 0/0 | 9918 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0042 | 0/0 | 9926 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0043 | 0/0 | 9918 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0044 | 0/0 | 9921 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0045 | 0/0 | 9921 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0046 | 0/0 | 10011 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0047 | 0/0 | 10012 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0048 | 0/0 | 10010 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0049 | 0/0 | 10011 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0050 | 0/0 | 10012 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0051 | 0/0 | 9937 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0052 | 0/0 | 9925 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0053 | 0/0 | 9921 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0054 | 0/0 | 9920 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0055 | 0/0 | 9918 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0056 | 0/0 | 9924 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0057 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0058 | 0/0 | 9928 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0059 | 0/0 | 9920 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0060 | 0/0 | 9924 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0061 | 0/0 | 9932 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0062 | 0/0 | 9926 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0063 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0064 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0065 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0066 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0067 | 0/0 | 9921 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0068 | 0/0 | 9925 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0069 | 0/0 | 9923 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0070 | 0/0 | 9925 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0071 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0072 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0073 | 0/0 | 9921 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0074 | 0/0 | 9924 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0075 | 0/0 | 9915 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0076 | 0/0 | 9927 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0077 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0078 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0079 | 0/0 | 9922 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0080 | 0/0 | 9922 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0081 | 0/0 | 9921 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0082 | 0/0 | 9921 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0083 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0084 | 0/0 | 9925 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0085 | 0/0 | 9934 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0086 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0087 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0088 | 0/0 | 9932 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0089 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0090 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0091 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0092 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0093 | 0/0 | 9934 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0094 | 0/0 | 9933 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0095 | 0/0 | 9926 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0096 | 0/0 | 9927 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0097 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0098 | 0/0 | 9932 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0099 | 0/0 | 9924 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0100 | 0/0 | 9932 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0101 | 0/0 | 9926 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0102 | 0/0 | 10010 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0103 | 0/0 | 10011 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| t0104 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0002 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0012 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1110 | 367 | 82 | 56 | 176 | 12 | 39 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002 | 0/0 | 1110 | 16 | 8 | 6 | 1 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0003 | 0/0 | 1110 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0004 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0005 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0002c0006 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11030 | 77 | 17 | 11 | 39 | 2 | 8 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0002 | 0/0 | 11034 | 28 | 1 | 7 | 11 | 3 | 6 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0003 | 0/0 | 11041 | 28 | 1 | 5 | 21 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0004 | 0/0 | 11035 | 23 | 3 | 6 | 9 | 1 | 4 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0005 | 1/0 | 11035 | 17 | 11 | 1 | 3 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0006 | 0/0 | 11035 | 15 | 0 | 0 | 13 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0007 | 0/0 | 11036 | 9 | 1 | 2 | 2 | 1 | 3 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0008 | 0/0 | 11045 | 8 | 8 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0009 | 0/0 | 11035 | 7 | 0 | 0 | 7 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0010 | 0/0 | 11120 | 6 | 3 | 2 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0011 | 0/0 | 11041 | 6 | 0 | 0 | 6 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0013 | 0/0 | 11041 | 6 | 0 | 0 | 6 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0014 | 0/0 | 11042 | 6 | 0 | 3 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0015 | 0/0 | 11119 | 6 | 1 | 4 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0016 | 0/0 | 11037 | 5 | 5 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0017 | 0/0 | 11030 | 5 | 0 | 0 | 5 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0018 | 0/1 | 11119 | 5 | 0 | 1 | 0 | 0 | 3 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0019 | 0/0 | 11029 | 4 | 2 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0021 | 0/0 | 11031 | 4 | 0 | 0 | 4 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0022 | 0/0 | 11035 | 3 | 3 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0023 | 0/0 | 11031 | 3 | 0 | 1 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0024 | 0/0 | 11030 | 3 | 0 | 2 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0025 | 0/0 | 11033 | 3 | 0 | 0 | 0 | 0 | 3 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0026 | 0/0 | 11030 | 3 | 0 | 0 | 2 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0027 | 0/0 | 11041 | 3 | 0 | 0 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0028 | 0/0 | 11035 | 3 | 0 | 1 | 0 | 2 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0029 | 0/0 | 11031 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0030 | 0/0 | 11045 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0031 | 0/0 | 11041 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0032 | 0/0 | 11033 | 2 | 0 | 0 | 1 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0033 | 0/0 | 11039 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0036 | 0/0 | 11036 | 2 | 1 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0037 | 0/0 | 11028 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0038 | 0/0 | 11032 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0039 | 0/0 | 11045 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0040 | 0/0 | 11034 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0042 | 0/0 | 11035 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0043 | 0/0 | 11027 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0044 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0045 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0046 | 0/0 | 11120 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0047 | 0/0 | 11121 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0048 | 0/0 | 11119 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0049 | 0/0 | 11120 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0050 | 0/0 | 11121 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0051 | 0/0 | 11046 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0052 | 0/0 | 11034 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0053 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0054 | 0/0 | 11029 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0055 | 0/0 | 11027 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0056 | 0/0 | 11033 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0057 | 0/0 | 11039 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0058 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0059 | 0/0 | 11029 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0060 | 0/0 | 11033 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0061 | 0/0 | 11041 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0062 | 0/0 | 11035 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0063 | 0/0 | 11039 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0065 | 0/0 | 11036 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0066 | 0/0 | 11030 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0067 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0068 | 0/0 | 11034 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0069 | 0/0 | 11032 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0071 | 0/0 | 11034 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0072 | 0/0 | 11036 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0073 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0074 | 0/0 | 11033 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0075 | 0/0 | 11024 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0076 | 0/0 | 11036 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0077 | 0/0 | 11034 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0078 | 0/0 | 11036 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0079 | 0/0 | 11031 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0080 | 0/0 | 11031 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0081 | 0/0 | 11030 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0082 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0083 | 0/0 | 11032 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0084 | 0/0 | 11034 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0085 | 0/0 | 11043 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0086 | 0/0 | 11041 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0087 | 0/0 | 11041 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0088 | 0/0 | 11041 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0089 | 0/0 | 11041 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0090 | 0/0 | 11039 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0091 | 0/0 | 11039 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0092 | 0/0 | 11039 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0093 | 0/0 | 11043 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0094 | 0/0 | 11042 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0095 | 0/0 | 11035 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0096 | 0/0 | 11036 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0097 | 0/0 | 11030 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0098 | 0/0 | 11041 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0099 | 0/0 | 11033 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0100 | 0/0 | 11041 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0101 | 0/0 | 11035 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0102 | 0/0 | 11119 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0103 | 0/0 | 11120 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0001t0104 | 0/0 | 11040 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002t0012 | 0/0 | 11033 | 6 | 2 | 2 | 1 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002t0020 | 0/0 | 11031 | 4 | 1 | 3 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002t0034 | 0/0 | 11029 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002t0035 | 0/0 | 11035 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002t0064 | 0/0 | 11028 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0002t0070 | 0/0 | 11034 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0003t0041 | 0/0 | 11027 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0004t0001 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0001c0005t0004 | 0/0 | 11035 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| a0002c0006t0004 | 0/0 | 11035 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | copy fasta | chr10 | 118671411 | 118759970 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0001 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0012 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0007g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0008g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0009g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0010g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0010g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0011g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0013g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0013g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0014g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0014g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0014g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0014g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0015g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0015g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0015g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0015g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0016g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0016g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0017g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0017g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0017g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0017g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0018g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0018g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0018g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0018g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0018g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0019g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0019g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0019g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0021g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0021g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0021g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0022g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0022g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0022g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0023g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0024g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0024g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0024g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0025g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0025g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0026g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0026g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0026g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0027g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0027g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0027g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0028g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0028g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0029g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0029g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0030g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0030g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0031g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0031g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0032g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0032g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0033g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0036g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0036g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0037g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0037g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0038g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0038g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0039g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0039g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0040g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0042g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0043g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0044g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0045g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0046g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0047g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0048g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0049g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0050g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0051g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0052g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0053g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0054g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0055g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0056g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0057g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0058g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0059g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0060g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0061g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0062g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0063g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0065g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0066g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0067g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0068g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0069g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0071g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0072g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0073g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0074g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0075g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0076g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0077g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0078g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0079g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0080g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0081g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0082g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0083g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0084g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0085g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0086g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0087g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0088g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0089g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0090g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0091g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0092g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0093g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0094g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0095g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0096g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0097g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0098g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0099g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0100g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0101g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0102g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0103g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0001t0104g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0012g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0012g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0012g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0012g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0020g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0020g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0020g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0020g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0034g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0034g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0035g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0064g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0002t0070g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0003t0041g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0003t0041g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0001c0005t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| a0002c0006t0004g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | GBR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0070 | EUR | FIN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00323 | hp2 | a0001 | c0001 | t0060 | g0321 | EUR | FIN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00423 | hp2 | a0001 | c0001 | t0085 | g0197 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00438 | hp1 | a0001 | c0001 | t0021 | g0243 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0006 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00544 | hp2 | a0001 | c0001 | t0037 | g0227 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00639 | hp2 | a0001 | c0001 | t0078 | g0332 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00673 | hp1 | a0001 | c0001 | t0053 | g0213 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00673 | hp2 | a0001 | c0001 | t0090 | g0171 | EAS | CHS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00735 | hp1 | a0001 | c0002 | t0012 | g0158 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0148 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01074 | hp1 | a0001 | c0001 | t0015 | g0199 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01081 | hp1 | a0001 | c0002 | t0070 | g0054 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01081 | hp2 | a0001 | c0001 | t0102 | g0139 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01099 | hp1 | a0001 | c0001 | t0099 | g0034 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01175 | hp2 | a0001 | c0001 | t0049 | g0138 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0136 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0155 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01243 | hp2 | a0001 | c0001 | t0101 | g0341 | AMR | PUR | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01261 | hp2 | a0001 | c0001 | t0081 | g0295 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0313 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01346 | hp2 | a0001 | c0001 | t0093 | g0246 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01496 | hp1 | a0001 | c0001 | t0023 | g0005 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01496 | hp2 | a0001 | c0001 | t0088 | g0176 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01515 | hp1 | a0001 | c0001 | t0028 | g0013 | EUR | IBS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01515 | hp2 | a0001 | c0001 | t0068 | g0323 | EUR | IBS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0304 | EUR | IBS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01516 | hp2 | a0001 | c0002 | t0012 | g0061 | EUR | IBS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01517 | hp1 | a0001 | c0001 | t0076 | g0305 | EUR | IBS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01517 | hp2 | a0001 | c0001 | t0028 | g0013 | EUR | IBS | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01884 | hp1 | a0001 | c0001 | t0036 | g0078 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01884 | hp2 | a0001 | c0001 | t0048 | g0200 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01891 | hp1 | a0001 | c0001 | t0046 | g0154 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01891 | hp2 | a0001 | c0001 | t0040 | g0014 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01934 | hp2 | a0001 | c0002 | t0020 | g0055 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01943 | hp2 | a0001 | c0002 | t0012 | g0150 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01975 | hp1 | a0001 | c0001 | t0014 | g0172 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01975 | hp2 | a0001 | c0001 | t0015 | g0020 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01978 | hp1 | a0001 | c0001 | t0014 | g0173 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0020 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01993 | hp1 | a0001 | c0001 | t0015 | g0141 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0325 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02004 | hp2 | a0001 | c0001 | t0024 | g0234 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0151 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02015 | hp2 | a0001 | c0001 | t0036 | g0087 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02027 | hp2 | a0001 | c0001 | t0087 | g0135 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02040 | hp1 | a0001 | c0001 | t0082 | g0250 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02071 | hp2 | a0001 | c0002 | t0012 | g0057 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02074 | hp1 | a0001 | c0001 | t0011 | g0101 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02083 | hp1 | a0001 | c0001 | t0023 | g0005 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02129 | hp2 | a0001 | c0001 | t0073 | g0226 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02145 | hp1 | a0001 | c0001 | t0022 | g0081 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02165 | hp2 | a0001 | c0001 | t0077 | g0031 | EAS | CDX | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0147 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02257 | hp2 | a0001 | c0001 | t0051 | g0048 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02258 | hp1 | a0001 | c0001 | t0066 | g0299 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02273 | hp1 | a0001 | c0002 | t0020 | g0063 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02273 | hp2 | a0001 | c0001 | t0024 | g0289 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02280 | hp1 | a0001 | c0001 | t0019 | g0298 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02280 | hp2 | a0001 | c0001 | t0091 | g0041 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02293 | hp1 | a0001 | c0002 | t0020 | g0056 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02293 | hp2 | a0001 | c0001 | t0103 | g0143 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02300 | hp1 | a0001 | c0001 | t0028 | g0077 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02300 | hp2 | a0001 | c0001 | t0065 | g0324 | AMR | PEL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02451 | hp1 | a0001 | c0001 | t0061 | g0049 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02602 | hp1 | a0001 | c0001 | t0018 | g0142 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0340 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02615 | hp1 | a0001 | c0001 | t0096 | g0317 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02615 | hp2 | a0001 | c0002 | t0012 | g0059 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0088 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02622 | hp2 | a0001 | c0002 | t0034 | g0058 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0153 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02630 | hp2 | a0001 | c0001 | t0030 | g0051 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02647 | hp1 | a0001 | c0002 | t0035 | g0008 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02698 | hp1 | a0001 | c0001 | t0050 | g0137 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0152 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02895 | hp1 | a0001 | c0001 | t0031 | g0053 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0047 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0096 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02970 | hp1 | a0001 | c0001 | t0016 | g0084 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02970 | hp2 | a0001 | c0001 | t0019 | g0220 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0080 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03017 | hp1 | a0001 | c0001 | t0018 | g0145 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03041 | hp2 | a0001 | c0002 | t0034 | g0062 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03098 | hp1 | a0001 | c0001 | t0030 | g0052 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03098 | hp2 | a0001 | c0001 | t0097 | g0222 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03130 | hp1 | a0001 | c0001 | t0039 | g0043 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03139 | hp1 | a0001 | c0001 | t0098 | g0040 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03139 | hp2 | a0001 | c0001 | t0052 | g0201 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03195 | hp2 | a0001 | c0002 | t0035 | g0008 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03225 | hp2 | a0001 | c0001 | t0040 | g0014 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03239 | hp1 | a0001 | c0001 | t0056 | g0068 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03453 | hp1 | a0001 | c0001 | t0022 | g0038 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03486 | hp1 | a0001 | c0001 | t0016 | g0011 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03486 | hp2 | a0001 | c0001 | t0083 | g0342 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03491 | hp2 | a0001 | c0003 | t0041 | g0209 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03492 | hp2 | a0001 | c0003 | t0041 | g0210 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03516 | hp1 | a0001 | c0001 | t0031 | g0050 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03516 | hp2 | a0001 | c0001 | t0079 | g0206 | AFR | ESN | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03579 | hp1 | a0001 | c0001 | t0092 | g0039 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03654 | hp1 | a0001 | c0001 | t0032 | g0076 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03654 | hp2 | a0001 | c0001 | t0025 | g0027 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03669 | hp1 | a0001 | c0001 | t0059 | g0264 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03669 | hp2 | a0001 | c0001 | t0025 | g0320 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0337 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03704 | hp2 | a0001 | c0001 | t0075 | g0230 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0071 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03710 | hp2 | a0002 | c0006 | t0004 | g0345 | SAS | PJL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0085 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0336 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0106 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0338 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04115 | hp2 | a0001 | c0001 | t0025 | g0027 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04184 | hp1 | a0001 | c0001 | t0018 | g0146 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04184 | hp2 | a0001 | c0001 | t0074 | g0322 | SAS | BEB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0335 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04228 | hp1 | a0001 | c0001 | t0026 | g0218 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0011 | AFR | YRI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18612 | hp1 | a0001 | c0001 | t0013 | g0179 | EAS | CHB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0108 | EAS | CHB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | CHB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | YRI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18939 | hp1 | a0001 | c0001 | t0015 | g0144 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18939 | hp2 | a0001 | c0001 | t0069 | g0247 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18940 | hp1 | a0001 | c0001 | t0011 | g0091 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18942 | hp2 | a0001 | c0001 | t0029 | g0103 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18947 | hp1 | a0001 | c0001 | t0067 | g0259 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18947 | hp2 | a0001 | c0001 | t0011 | g0094 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18948 | hp1 | a0001 | c0001 | t0024 | g0245 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18950 | hp1 | a0001 | c0001 | t0009 | g0092 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18950 | hp2 | a0001 | c0001 | t0086 | g0190 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18952 | hp2 | a0001 | c0001 | t0017 | g0022 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18954 | hp1 | a0001 | c0001 | t0058 | g0090 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18954 | hp2 | a0001 | c0001 | t0013 | g0006 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18956 | hp2 | a0001 | c0001 | t0063 | g0126 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0301 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18961 | hp1 | a0001 | c0004 | t0001 | g0030 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18961 | hp2 | a0001 | c0001 | t0033 | g0017 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18963 | hp2 | a0001 | c0001 | t0043 | g0181 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18967 | hp1 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0105 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18975 | hp1 | a0001 | c0001 | t0027 | g0187 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18977 | hp2 | a0001 | c0001 | t0014 | g0169 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18983 | hp1 | a0001 | c0001 | t0038 | g0211 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18984 | hp1 | a0001 | c0001 | t0045 | g0212 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18985 | hp1 | a0001 | c0001 | t0072 | g0035 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18986 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18990 | hp1 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18990 | hp2 | a0001 | c0001 | t0019 | g0255 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18991 | hp1 | a0001 | c0001 | t0094 | g0182 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18991 | hp2 | a0001 | c0001 | t0026 | g0217 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18994 | hp2 | a0001 | c0001 | t0017 | g0022 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18995 | hp2 | a0001 | c0001 | t0017 | g0231 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18998 | hp1 | a0001 | c0001 | t0033 | g0017 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19000 | hp1 | a0001 | c0001 | t0013 | g0194 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0005 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19002 | hp2 | a0001 | c0001 | t0089 | g0160 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19004 | hp1 | a0001 | c0001 | t0042 | g0111 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19004 | hp2 | a0001 | c0001 | t0021 | g0025 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19011 | hp1 | a0001 | c0001 | t0062 | g0109 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19011 | hp2 | a0001 | c0001 | t0014 | g0162 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19012 | hp1 | a0001 | c0001 | t0054 | g0258 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19012 | hp2 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19030 | hp1 | a0001 | c0002 | t0020 | g0060 | AFR | LWK | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | LWK | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19043 | hp1 | a0001 | c0002 | t0064 | g0149 | AFR | LWK | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | LWK | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19054 | hp1 | a0001 | c0001 | t0014 | g0175 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19054 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19057 | hp1 | a0001 | c0001 | t0017 | g0232 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19057 | hp2 | a0001 | c0001 | t0027 | g0188 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19060 | hp2 | a0001 | c0001 | t0104 | g0131 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19063 | hp2 | a0001 | c0001 | t0071 | g0064 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19065 | hp2 | a0001 | c0001 | t0013 | g0006 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19067 | hp1 | a0001 | c0001 | t0013 | g0195 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19067 | hp2 | a0001 | c0001 | t0017 | g0254 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19068 | hp1 | a0001 | c0001 | t0026 | g0235 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19068 | hp2 | a0001 | c0001 | t0007 | g0314 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19070 | hp1 | a0001 | c0001 | t0044 | g0225 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19070 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19074 | hp2 | a0001 | c0001 | t0100 | g0191 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19077 | hp2 | a0001 | c0001 | t0027 | g0185 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19078 | hp1 | a0001 | c0001 | t0029 | g0115 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19078 | hp2 | a0001 | c0001 | t0037 | g0216 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19080 | hp1 | a0001 | c0001 | t0021 | g0025 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19080 | hp2 | a0001 | c0001 | t0032 | g0072 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19081 | hp2 | a0001 | c0001 | t0057 | g0089 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19088 | hp1 | a0001 | c0001 | t0038 | g0233 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19240 | hp1 | a0001 | c0002 | t0012 | g0037 | AFR | YRI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA19240 | hp2 | a0001 | c0001 | t0039 | g0042 | AFR | YRI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | TSI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20805 | hp1 | a0001 | c0005 | t0004 | g0069 | EUR | TSI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0309 | EUR | TSI | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20905 | hp1 | a0001 | c0001 | t0055 | g0067 | SAS | GIH | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | GIH | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG01123 | hp2 | a0001 | c0001 | t0014 | g0180 | AMR | CLM | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0202 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02109 | hp2 | a0001 | c0001 | t0080 | g0205 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02486 | hp1 | a0001 | c0001 | t0095 | g0036 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG02559 | hp2 | a0001 | c0001 | t0084 | g0343 | AFR | ACB | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03471 | hp1 | a0001 | c0001 | t0047 | g0156 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | USA | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | USA | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18955 | hp1 | a0001 | c0001 | t0021 | g0251 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | USA | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | USA | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | LWK | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | LWK | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0018 | g0140 | REF | REF | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0099 | REF | REF | CACUL1_chr10_118671411_118759970 | CACUL1 | chr10 | 118671411 | 118759970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:118754626
|
G | A | 1 | a0002 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.137C>T | p.Pro46Leu | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/9 | 345/11035 | 137/1110 | 46/369 | chr10 | 118754626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:118686602
|
A | G | 1 | a0001c0002 | 16 | HG00735.hp1 HG01081.hp1 HG01516.hp2 others(13): Show |
synonymous_variant | LOW | c.1065T>C | p.Ala355Ala | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 8/9 | 1273/11035 | 1065/1110 | 355/369 | chr10 | 118686602 | ||
| chr10:118691366
|
A | G | 1 | a0001c0003 | 2 | HG03491.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.924T>C | p.Phe308Phe | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/9 | 1132/11035 | 924/1110 | 308/369 | chr10 | 118691366 | ||
| chr10:118730316
|
G | A | 1 | a0001c0005 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.462C>T | p.Asp154Asp | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 2/9 | 670/11035 | 462/1110 | 154/369 | chr10 | 118730316 | ||
| chr10:118754598
|
C | T | 1 | a0001c0004 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.165G>A | p.Gly55Gly | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/9 | 373/11035 | 165/1110 | 55/369 | chr10 | 118754598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:118676733
|
A | G | 1 | a0001c0001t0088 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9395T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9395 | chr10 | 118676733 | |||||
| chr10:118676808
|
A | G | 24 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(21): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*9320T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9320 | chr10 | 118676808 | |||||
| chr10:118676839
|
T | TAC | 2 | a0001c0001t0016a0001c0001t0058 | 6 | HG02109.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9287_*9288dupGT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9288 | chr10 | 118676839 | |||||
| chr10:118676839
|
T | TACAC | 3 | a0001c0001t0033a0001c0001t0057a0001c0001t0063 | 4 | NA18956.hp2 NA18961.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9285_*9288dupGTGT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9288 | chr10 | 118676839 | |||||
| chr10:118676839
|
T | TACACAC | 2 | a0001c0001t0011a0001c0001t0104 | 7 | HG02074.hp1 NA18940.hp1 NA18947.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9283_*9288dupGTGT others(2): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9288 | chr10 | 118676839 | |||||
| chr10:118676839
|
TAC | T | 11 | a0001c0001t0002a0001c0001t0032a0001c0001t0040others(8): Show | 45 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*9287_*9288delGT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9287 | chr10 | 118676839 | |||||
| chr10:118676839
|
TACAC | T | 15 | a0001c0001t0008a0001c0001t0023a0001c0001t0025others(12): Show | 34 | HG01099.hp1 HG01496.hp1 HG01934.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*9285_*9288delGTGT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9285 | chr10 | 118676839 | |||||
| chr10:118676839
|
TACACAC | T | 24 | a0001c0001t0001a0001c0001t0017a0001c0001t0019others(21): Show | 115 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*9283_*9288delGTGT others(2): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9283 | chr10 | 118676839 | |||||
| chr10:118676839
|
TACACACA others(1): Show |
T | 25 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(22): Show | 80 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*9281_*9288delGTGT others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9281 | chr10 | 118676839 | |||||
| chr10:118676839
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0048a0001c0001t0052a0001c0001t0091others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9279_*9288delGTGT others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9279 | chr10 | 118676839 | |||||
| chr10:118676839
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0075 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9277_*9288delGTGT others(8): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9277 | chr10 | 118676839 | |||||
| chr10:118676872
|
A | C | 3 | a0001c0001t0091a0001c0001t0092a0001c0001t0098 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9256T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9256 | chr10 | 118676872 | |||||
| chr10:118676872
|
A | G | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(72): Show | 278 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*9256T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9256 | chr10 | 118676872 | |||||
| chr10:118676891
|
G | A | 1 | a0001c0001t0017 | 5 | NA18952.hp2 NA18994.hp2 NA18995.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9237C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9237 | chr10 | 118676891 | |||||
| chr10:118676936
|
T | C | 13 | a0001c0001t0004a0001c0001t0009a0001c0001t0023others(10): Show | 46 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*9192A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9192 | chr10 | 118676936 | |||||
| chr10:118676961
|
C | A | 3 | a0001c0001t0013a0001c0001t0043a0001c0001t0094 | 8 | HG00544.hp1 NA18612.hp1 NA18954.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9167G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9167 | chr10 | 118676961 | |||||
| chr10:118677072
|
G | A | 1 | a0001c0001t0058 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9056C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 9056 | chr10 | 118677072 | |||||
| chr10:118677223
|
G | C | 25 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(22): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8905C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8905 | chr10 | 118677223 | |||||
| chr10:118677231
|
A | G | 1 | a0001c0001t0056 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8897T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8897 | chr10 | 118677231 | |||||
| chr10:118677253
|
A | G | 2 | a0001c0001t0015a0001c0001t0103 | 7 | HG01074.hp1 HG01975.hp2 HG01981.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8875T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8875 | chr10 | 118677253 | |||||
| chr10:118677254
|
T | TA | 34 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(31): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*8873_*8874insT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8873 | chr10 | 118677254 | |||||
| chr10:118677434
|
G | A | 1 | a0001c0001t0063 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8694C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8694 | chr10 | 118677434 | |||||
| chr10:118677495
|
A | C | 2 | a0001c0001t0083a0001c0001t0084 | 2 | HG02559.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8633T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8633 | chr10 | 118677495 | |||||
| chr10:118677556
|
C | T | 1 | a0001c0001t0087 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8572G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8572 | chr10 | 118677556 | |||||
| chr10:118677627
|
T | A | 1 | a0001c0001t0074 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8501A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8501 | chr10 | 118677627 | |||||
| chr10:118677847
|
C | T | 25 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(22): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8281G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8281 | chr10 | 118677847 | |||||
| chr10:118678045
|
A | G | 1 | a0001c0001t0059 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8083T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8083 | chr10 | 118678045 | |||||
| chr10:118678046
|
T | C | 2 | a0001c0001t0083a0001c0001t0084 | 2 | HG02559.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8082A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 8082 | chr10 | 118678046 | |||||
| chr10:118678151
|
G | A | 2 | a0001c0001t0008a0001c0001t0039 | 10 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7977C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7977 | chr10 | 118678151 | |||||
| chr10:118678365
|
C | A | 1 | a0001c0001t0049 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7763G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7763 | chr10 | 118678365 | |||||
| chr10:118678475
|
T | C | 6 | a0001c0001t0008a0001c0001t0010a0001c0001t0039others(3): Show | 19 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7653A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7653 | chr10 | 118678475 | |||||
| chr10:118678485
|
C | A | 34 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(31): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*7643G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7643 | chr10 | 118678485 | |||||
| chr10:118678509
|
G | A | 1 | a0001c0001t0089 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7619C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7619 | chr10 | 118678509 | |||||
| chr10:118678516
|
T | C | 1 | a0001c0001t0062 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7612A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7612 | chr10 | 118678516 | |||||
| chr10:118678619
|
G | GT | 7 | a0001c0001t0025a0001c0001t0040a0001c0001t0052others(4): Show | 10 | HG01099.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7508dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7508 | chr10 | 118678619 | |||||
| chr10:118678619
|
G | GTT | 32 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(29): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*7507_*7508dupAA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7508 | chr10 | 118678619 | |||||
| chr10:118678885
|
C | T | 1 | a0001c0001t0086 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7243G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7243 | chr10 | 118678885 | |||||
| chr10:118678973
|
G | A | 1 | a0001c0001t0092 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7155C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7155 | chr10 | 118678973 | |||||
| chr10:118679095
|
A | T | 33 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(30): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*7033T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 7033 | chr10 | 118679095 | |||||
| chr10:118679153
|
A | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(36): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*6975T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6975 | chr10 | 118679153 | |||||
| chr10:118679377
|
A | ATTTTTAT | 34 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(31): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*6744_*6750dupATAA others(3): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6750 | chr10 | 118679377 | |||||
| chr10:118679404
|
C | T | 1 | a0001c0001t0055 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6724G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6724 | chr10 | 118679404 | |||||
| chr10:118679457
|
C | G | 1 | a0001c0001t0073 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6671G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6671 | chr10 | 118679457 | |||||
| chr10:118679527
|
G | A | 1 | a0001c0001t0103 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6601C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6601 | chr10 | 118679527 | |||||
| chr10:118679614
|
G | A | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(36): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*6514C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6514 | chr10 | 118679614 | |||||
| chr10:118680000
|
T | C | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6128A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6128 | chr10 | 118680000 | |||||
| chr10:118680046
|
G | A | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6082C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 6082 | chr10 | 118680046 | |||||
| chr10:118680249
|
G | C | 1 | a0001c0001t0061 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5879C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 5879 | chr10 | 118680249 | |||||
| chr10:118680409
|
A | G | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5719T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 5719 | chr10 | 118680409 | |||||
| chr10:118680651
|
C | T | 1 | a0001c0001t0039 | 2 | HG03130.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5477G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 5477 | chr10 | 118680651 | |||||
| chr10:118680668
|
C | G | 1 | a0001c0001t0104 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5460G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 5460 | chr10 | 118680668 | |||||
| chr10:118680707
|
C | T | 1 | a0001c0001t0079 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5421G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 5421 | chr10 | 118680707 | |||||
| chr10:118680839
|
T | G | 1 | a0001c0001t0026 | 3 | HG04228.hp1 NA18991.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5289A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 5289 | chr10 | 118680839 | |||||
| chr10:118681134
|
C | T | 1 | a0001c0001t0044 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4994G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4994 | chr10 | 118681134 | |||||
| chr10:118681209
|
T | C | 5 | a0001c0001t0006a0001c0001t0029a0001c0001t0042others(2): Show | 20 | HG02165.hp2 HG03710.hp1 HG03942.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4919A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4919 | chr10 | 118681209 | |||||
| chr10:118681271
|
G | A | 1 | a0001c0001t0078 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4857C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4857 | chr10 | 118681271 | |||||
| chr10:118681420
|
C | T | 2 | a0001c0001t0024a0001c0001t0069 | 4 | HG02004.hp2 HG02273.hp2 NA18939.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4708G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4708 | chr10 | 118681420 | |||||
| chr10:118681437
|
C | T | 13 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(10): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4691G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4691 | chr10 | 118681437 | |||||
| chr10:118681615
|
A | G | 1 | a0001c0001t0068 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4513T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4513 | chr10 | 118681615 | |||||
| chr10:118681638
|
C | T | 1 | a0001c0001t0085 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4490G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4490 | chr10 | 118681638 | |||||
| chr10:118681763
|
C | T | 15 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(12): Show | 54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*4365G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 4365 | chr10 | 118681763 | |||||
| chr10:118682409
|
G | A | 4 | a0001c0001t0011a0001c0001t0033a0001c0001t0063others(1): Show | 10 | HG02074.hp1 NA18940.hp1 NA18947.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3719C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3719 | chr10 | 118682409 | |||||
| chr10:118682411
|
A | G | 1 | a0001c0001t0082 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3717T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3717 | chr10 | 118682411 | |||||
| chr10:118682442
|
G | A | 5 | a0001c0002t0012a0001c0002t0020a0001c0002t0034others(2): Show | 15 | HG00735.hp1 HG01516.hp2 HG01934.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3686C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3686 | chr10 | 118682442 | |||||
| chr10:118682588
|
C | T | 1 | a0001c0001t0066 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3540G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3540 | chr10 | 118682588 | |||||
| chr10:118682624
|
G | A | 2 | a0001c0001t0079a0001c0001t0080 | 2 | HG02109.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3504C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3504 | chr10 | 118682624 | |||||
| chr10:118682625
|
T | A | 1 | a0001c0001t0081 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3503A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3503 | chr10 | 118682625 | |||||
| chr10:118682634
|
C | T | 1 | a0001c0001t0102 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3494G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3494 | chr10 | 118682634 | |||||
| chr10:118682781
|
G | C | 1 | a0001c0001t0082 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3347 | chr10 | 118682781 | |||||
| chr10:118682821
|
A | G | 1 | a0001c0001t0096 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3307T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3307 | chr10 | 118682821 | |||||
| chr10:118682843
|
C | G | 1 | a0001c0001t0065 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3285G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3285 | chr10 | 118682843 | |||||
| chr10:118683002
|
C | T | 1 | a0001c0001t0046 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3126G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 3126 | chr10 | 118683002 | |||||
| chr10:118683193
|
C | T | 1 | a0001c0001t0102 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2935G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2935 | chr10 | 118683193 | |||||
| chr10:118683308
|
T | A | 2 | a0001c0001t0083a0001c0001t0084 | 2 | HG02559.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2820A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2820 | chr10 | 118683308 | |||||
| chr10:118683370
|
T | C | 10 | a0001c0001t0010a0001c0001t0015a0001c0001t0018others(7): Show | 24 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2758A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2758 | chr10 | 118683370 | |||||
| chr10:118683389
|
C | CA | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(36): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2738dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2738 | chr10 | 118683389 | |||||
| chr10:118683389
|
C | CAAAA | 25 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(22): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2735_*2738dupTTTT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2738 | chr10 | 118683389 | |||||
| chr10:118683389
|
C | CAAAAA | 6 | a0001c0001t0014a0001c0001t0048a0001c0001t0050others(3): Show | 11 | HG01123.hp2 HG01884.hp2 HG01975.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2734_*2738dupTTTT others(1): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2738 | chr10 | 118683389 | |||||
| chr10:118683456
|
G | A | 1 | a0001c0001t0027 | 3 | NA18975.hp1 NA19057.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2672C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2672 | chr10 | 118683456 | |||||
| chr10:118683596
|
G | A | 1 | a0001c0001t0095 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2532C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2532 | chr10 | 118683596 | |||||
| chr10:118683688
|
C | T | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2440G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2440 | chr10 | 118683688 | |||||
| chr10:118683798
|
T | A | 1 | a0001c0001t0096 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2330 | chr10 | 118683798 | |||||
| chr10:118683899
|
C | T | 1 | a0001c0001t0022 | 3 | HG02145.hp1 HG02976.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2229G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2229 | chr10 | 118683899 | |||||
| chr10:118683963
|
T | TA | 1 | a0001c0001t0021 | 4 | HG00438.hp1 NA18955.hp1 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2164_*2165insT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2164 | chr10 | 118683963 | |||||
| chr10:118683986
|
T | C | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2142A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2142 | chr10 | 118683986 | |||||
| chr10:118684070
|
T | C | 1 | a0001c0001t0097 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2058A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 2058 | chr10 | 118684070 | |||||
| chr10:118684300
|
C | T | 1 | a0001c0001t0053 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 1828 | chr10 | 118684300 | |||||
| chr10:118684512
|
T | C | 1 | a0001c0001t0098 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1616A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 1616 | chr10 | 118684512 | |||||
| chr10:118684578
|
A | C | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1550T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 1550 | chr10 | 118684578 | |||||
| chr10:118684779
|
C | T | 1 | a0001c0001t0051 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 1349 | chr10 | 118684779 | |||||
| chr10:118684972
|
A | T | 1 | a0001c0001t0030 | 2 | HG02630.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1156T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 1156 | chr10 | 118684972 | |||||
| chr10:118685008
|
G | C | 1 | a0001c0001t0099 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1120C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 1120 | chr10 | 118685008 | |||||
| chr10:118685130
|
C | T | 4 | a0001c0001t0010a0001c0001t0046a0001c0001t0047others(1): Show | 9 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*998G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 998 | chr10 | 118685130 | |||||
| chr10:118685161
|
T | A | 1 | a0001c0001t0009 | 7 | NA18950.hp1 NA18957.hp2 NA18967.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*967A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 967 | chr10 | 118685161 | |||||
| chr10:118685166
|
T | G | 1 | a0001c0001t0028 | 3 | HG01515.hp1 HG01517.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*962A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 962 | chr10 | 118685166 | |||||
| chr10:118685179
|
G | A | 1 | a0001c0001t0100 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*949C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 949 | chr10 | 118685179 | |||||
| chr10:118685271
|
G | GGTGACAG others(72): Show |
10 | a0001c0001t0010a0001c0001t0015a0001c0001t0018others(7): Show | 24 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*778_*856dupGCATAT others(73): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 856 | chr10 | 118685271 | |||||
| chr10:118685368
|
A | C | 10 | a0001c0001t0010a0001c0001t0015a0001c0001t0018others(7): Show | 24 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*760T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 760 | chr10 | 118685368 | |||||
| chr10:118685373
|
C | T | 1 | a0001c0001t0029 | 2 | NA18942.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*755G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 755 | chr10 | 118685373 | |||||
| chr10:118685446
|
G | A | 1 | a0001c0001t0101 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 682 | chr10 | 118685446 | |||||
| chr10:118685568
|
T | C | 1 | a0001c0001t0040 | 2 | HG01891.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*560A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 560 | chr10 | 118685568 | |||||
| chr10:118685763
|
A | C | 2 | a0001c0001t0044a0001c0001t0045 | 2 | NA18984.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*365T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 365 | chr10 | 118685763 | |||||
| chr10:118685835
|
TTCACTTA others(7): Show |
T | 1 | a0001c0001t0043 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279_*292delCCATTT others(8): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 279 | chr10 | 118685835 | |||||
| chr10:118685865
|
C | T | 1 | a0001c0001t0042 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 263 | chr10 | 118685865 | |||||
| chr10:118685944
|
GT | G | 6 | a0001c0001t0015a0001c0001t0018a0001c0001t0102others(3): Show | 16 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*183delA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 9/9 | 183 | chr10 | 118685944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:118686270
|
TC | T | 14 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(11): Show | 15 | HG00735.hp1 HG01516.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1070-103delG | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 8/8 | chr10 | 118686270 | ||||||
| chr10:118686282
|
G | A | 100 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(97): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1070-114C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 8/8 | chr10 | 118686282 | ||||||
| chr10:118686285
|
T | TA | 6 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(3): Show | 6 | HG01099.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070-118dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 8/8 | chr10 | 118686285 | ||||||
| chr10:118686364
|
G | C | 1 | a0001c0001t0009g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1070-196C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 8/8 | chr10 | 118686364 | ||||||
| chr10:118686391
|
C | T | 1 | a0001c0001t0078g0332 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1069+207G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 8/8 | chr10 | 118686391 | ||||||
| chr10:118686722
|
G | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1026-81C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118686722 | ||||||
| chr10:118686838
|
G | GT | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-198dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118686838 | ||||||
| chr10:118686885
|
T | A | 67 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(64): Show | 76 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1026-244A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118686885 | ||||||
| chr10:118686982
|
C | A | 1 | a0001c0001t0003g0178 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1026-341G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118686982 | ||||||
| chr10:118687284
|
C | T | 2 | a0001c0001t0031g0050a0001c0001t0031g0053 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1026-643G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687284 | ||||||
| chr10:118687316
|
C | A | 23 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(20): Show | 24 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1026-675G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687316 | ||||||
| chr10:118687455
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(239): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1026-814A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687455 | ||||||
| chr10:118687476
|
T | C | 1 | a0001c0001t0015g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1026-835A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687476 | ||||||
| chr10:118687826
|
A | AT | 12 | a0001c0001t0015g0020a0001c0001t0015g0141a0001c0001t0015g0144others(9): Show | 13 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1026-1186dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687826 | ||||||
| chr10:118687877
|
A | G | 5 | a0001c0001t0009g0004a0001c0001t0009g0092a0001c0001t0009g0093others(2): Show | 7 | NA18950.hp1 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-1236T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687877 | ||||||
| chr10:118687907
|
G | A | 14 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(11): Show | 16 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1026-1266C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687907 | ||||||
| chr10:118687917
|
C | T | 34 | a0001c0001t0001g0024a0001c0001t0001g0215a0001c0001t0001g0223others(31): Show | 36 | HG00423.hp1 HG00438.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1026-1276G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687917 | ||||||
| chr10:118687925
|
C | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(96): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1026-1284G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687925 | ||||||
| chr10:118687937
|
T | C | 8 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(5): Show | 10 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-1296A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687937 | ||||||
| chr10:118687978
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1026-1337A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118687978 | ||||||
| chr10:118688096
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026-1455C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688096 | ||||||
| chr10:118688531
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0214 | 3 | HG03239.hp2 HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1026-1890G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688531 | ||||||
| chr10:118688533
|
A | G | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1026-1892T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688533 | ||||||
| chr10:118688550
|
G | A | 1 | a0001c0001t0029g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1026-1909C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688550 | ||||||
| chr10:118688595
|
C | T | 1 | a0001c0001t0025g0320 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1026-1954G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688595 | ||||||
| chr10:118688691
|
A | G | 9 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(6): Show | 9 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026-2050T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688691 | ||||||
| chr10:118688723
|
C | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0012a0001c0001t0004g0065others(23): Show | 36 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-2082G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688723 | ||||||
| chr10:118688750
|
T | C | 6 | a0001c0001t0007g0304a0001c0001t0007g0313a0001c0001t0007g0325others(3): Show | 6 | HG01346.hp1 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-2109A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688750 | ||||||
| chr10:118688764
|
A | G | 1 | a0001c0001t0102g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1026-2123T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118688764 | ||||||
| chr10:118689037
|
G | A | 1 | a0001c0001t0002g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1025+2228C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689037 | ||||||
| chr10:118689058
|
A | G | 84 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(81): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1025+2207T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689058 | ||||||
| chr10:118689317
|
C | T | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1025+1948G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689317 | ||||||
| chr10:118689330
|
G | A | 3 | a0001c0001t0004g0070a0001c0001t0056g0068a0001c0005t0004g0069 | 3 | HG00323.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1025+1935C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689330 | ||||||
| chr10:118689455
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1025+1810T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689455 | ||||||
| chr10:118689510
|
T | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0261 | 2 | HG01070.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1025+1755A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689510 | ||||||
| chr10:118689604
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(239): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1025+1661A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689604 | ||||||
| chr10:118689678
|
C | A | 3 | a0001c0001t0006g0108a0001c0001t0006g0124a0001c0001t0062g0109 | 3 | NA18612.hp2 NA18974.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1025+1587G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689678 | ||||||
| chr10:118689716
|
CCT | C | 14 | a0001c0001t0015g0020a0001c0001t0015g0141a0001c0001t0015g0144others(11): Show | 15 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1025+1547_1025+154 others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118689716 | ||||||
| chr10:118690047
|
G | A | 9 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(6): Show | 9 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025+1218C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690047 | ||||||
| chr10:118690195
|
G | A | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1025+1070C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690195 | ||||||
| chr10:118690214
|
T | C | 2 | a0001c0001t0007g0325a0001c0001t0065g0324 | 2 | HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1025+1051A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690214 | ||||||
| chr10:118690258
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1025+1007C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690258 | ||||||
| chr10:118690271
|
G | A | 64 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(61): Show | 73 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1025+994C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690271 | ||||||
| chr10:118690295
|
G | A | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1025+970C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690295 | ||||||
| chr10:118690307
|
C | CA | 121 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(118): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1025+957dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
C | CAA | 21 | a0001c0001t0001g0204a0001c0001t0001g0208a0001c0001t0001g0249others(18): Show | 21 | HG01074.hp2 HG01106.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1025+956_1025+957d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
C | CAAAAAA | 8 | a0001c0001t0001g0297a0001c0001t0001g0300a0001c0001t0008g0009others(5): Show | 9 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025+952_1025+957d others(8): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
C | CAAAAAAA | 7 | a0001c0001t0008g0010a0001c0001t0008g0045a0001c0001t0008g0046others(4): Show | 8 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+951_1025+957d others(9): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
CA | C | 80 | a0001c0001t0004g0001a0001c0001t0004g0012a0001c0001t0004g0065others(77): Show | 96 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.1025+957delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
CAAA | C | 6 | a0001c0001t0003g0166a0001c0001t0003g0184a0001c0001t0013g0194others(3): Show | 6 | HG01978.hp1 HG02602.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025+955_1025+957d others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
CAAAA | C | 61 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(58): Show | 70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1025+954_1025+957d others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690307
|
CAAAAAA | C | 14 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(11): Show | 15 | HG00735.hp1 HG01516.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1025+952_1025+957d others(8): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690307 | ||||||
| chr10:118690529
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1025+736A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690529 | ||||||
| chr10:118690583
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1025+682C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118690583 | ||||||
| chr10:118691104
|
T | C | 5 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0165others(2): Show | 5 | NA18942.hp1 NA18948.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+161A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118691104 | ||||||
| chr10:118691125
|
A | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1025+140T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 7/8 | chr10 | 118691125 | ||||||
| chr10:118691471
|
A | C | 1 | a0001c0001t0008g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.887-68T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691471 | ||||||
| chr10:118691615
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.887-212G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691615 | ||||||
| chr10:118691791
|
T | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(253): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.887-388A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691791 | ||||||
| chr10:118691866
|
C | CA | 100 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(97): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.887-464dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691866 | ||||||
| chr10:118691866
|
C | CAA | 18 | a0001c0001t0001g0032a0001c0001t0001g0241a0001c0001t0001g0242others(15): Show | 18 | HG00673.hp1 HG01106.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.887-465_887-464dup others(2): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691866 | ||||||
| chr10:118691866
|
C | CAAAAA | 5 | a0001c0001t0008g0010a0001c0001t0008g0044a0001c0001t0008g0045others(2): Show | 6 | HG02559.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.887-468_887-464dup others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691866 | ||||||
| chr10:118691866
|
CA | C | 79 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(76): Show | 89 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.887-464delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691866 | ||||||
| chr10:118691866
|
CAAAAAAA others(3): Show |
C | 44 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(41): Show | 49 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.887-473_887-464del others(10): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691866 | ||||||
| chr10:118691884
|
A | G | 15 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(12): Show | 16 | HG00735.hp1 HG01081.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.887-481T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691884 | ||||||
| chr10:118691958
|
C | A | 1 | a0001c0001t0003g0019 | 2 | NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.887-555G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118691958 | ||||||
| chr10:118692190
|
G | A | 1 | a0001c0001t0061g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.887-787C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118692190 | ||||||
| chr10:118692442
|
T | C | 1 | a0001c0001t0005g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.887-1039A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118692442 | ||||||
| chr10:118692452
|
A | G | 1 | a0001c0001t0032g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.887-1049T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118692452 | ||||||
| chr10:118692476
|
A | T | 12 | a0001c0001t0015g0020a0001c0001t0015g0141a0001c0001t0015g0144others(9): Show | 13 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1073T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118692476 | ||||||
| chr10:118692931
|
T | A | 1 | a0001c0001t0002g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.887-1528A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118692931 | ||||||
| chr10:118693142
|
G | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(238): Show | 266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.887-1739C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118693142 | ||||||
| chr10:118693534
|
C | T | 5 | a0001c0001t0001g0208a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02523.hp2 NA18959.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.886+1607G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118693534 | ||||||
| chr10:118693656
|
T | C | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.886+1485A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118693656 | ||||||
| chr10:118693691
|
C | G | 1 | a0001c0001t0011g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.886+1450G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118693691 | ||||||
| chr10:118693928
|
T | C | 1 | a0001c0001t0018g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.886+1213A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118693928 | ||||||
| chr10:118693978
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.886+1163T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118693978 | ||||||
| chr10:118694083
|
C | G | 1 | a0001c0001t0104g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.886+1058G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694083 | ||||||
| chr10:118694102
|
G | C | 2 | a0001c0001t0001g0275a0001c0001t0001g0339 | 2 | HG01167.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.886+1039C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694102 | ||||||
| chr10:118694110
|
C | A | 14 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(11): Show | 15 | HG00735.hp1 HG01516.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1031G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694110 | ||||||
| chr10:118694111
|
G | A | 1 | a0002c0006t0004g0345 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.886+1030C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694111 | ||||||
| chr10:118694528
|
G | GA | 7 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+612dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694528 | ||||||
| chr10:118694556
|
G | A | 1 | a0001c0001t0096g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.886+585C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694556 | ||||||
| chr10:118694972
|
C | T | 1 | a0001c0001t0104g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.886+169G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 6/8 | chr10 | 118694972 | ||||||
| chr10:118695244
|
A | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.797-14T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118695244 | ||||||
| chr10:118695456
|
T | C | 1 | a0001c0001t0031g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.797-226A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118695456 | ||||||
| chr10:118695767
|
C | T | 2 | a0001c0001t0030g0051a0001c0001t0030g0052 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.797-537G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118695767 | ||||||
| chr10:118695907
|
A | G | 2 | a0001c0001t0030g0051a0001c0001t0030g0052 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.797-677T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118695907 | ||||||
| chr10:118695917
|
GACCTAAA | G | 85 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(82): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.797-694_797-688del others(7): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118695917 | ||||||
| chr10:118696006
|
G | C | 21 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(18): Show | 22 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.797-776C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696006 | ||||||
| chr10:118696105
|
C | T | 23 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(20): Show | 24 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.797-875G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696105 | ||||||
| chr10:118696187
|
C | T | 1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.797-957G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696187 | ||||||
| chr10:118696394
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0079others(5): Show | 11 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.797-1164T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696394 | ||||||
| chr10:118696488
|
A | G | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.797-1258T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696488 | ||||||
| chr10:118696505
|
G | A | 1 | a0001c0001t0088g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.797-1275C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696505 | ||||||
| chr10:118696661
|
G | A | 2 | a0001c0001t0004g0128a0001c0001t0004g0129 | 2 | HG01361.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.797-1431C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696661 | ||||||
| chr10:118696828
|
T | C | 1 | a0001c0001t0028g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.797-1598A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696828 | ||||||
| chr10:118696986
|
G | GATAGCT | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.797-1757_797-1756i others(8): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118696986 | ||||||
| chr10:118697253
|
T | G | 1 | a0001c0001t0042g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.797-2023A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118697253 | ||||||
| chr10:118697400
|
T | C | 16 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(13): Show | 18 | HG01175.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.797-2170A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118697400 | ||||||
| chr10:118697537
|
C | T | 4 | a0001c0001t0005g0086a0001c0001t0016g0084a0001c0001t0016g0096others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-2307G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118697537 | ||||||
| chr10:118697759
|
T | G | 1 | a0001c0001t0104g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.797-2529A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118697759 | ||||||
| chr10:118698080
|
T | C | 1 | a0001c0001t0027g0185 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.797-2850A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698080 | ||||||
| chr10:118698147
|
G | A | 2 | a0001c0001t0002g0312a0001c0001t0002g0334 | 2 | HG00609.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.797-2917C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698147 | ||||||
| chr10:118698148
|
C | CT | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0219others(7): Show | 10 | HG01243.hp2 HG02809.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.797-2919dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698148 | ||||||
| chr10:118698191
|
G | T | 1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.797-2961C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698191 | ||||||
| chr10:118698359
|
G | C | 1 | a0001c0001t0004g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.796+2947C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698359 | ||||||
| chr10:118698433
|
C | T | 13 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(10): Show | 14 | HG00735.hp1 HG01516.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+2873G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698433 | ||||||
| chr10:118698435
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.796+2871G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698435 | ||||||
| chr10:118698507
|
G | A | 2 | a0001c0001t0049g0138a0001c0001t0050g0137 | 2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.796+2799C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698507 | ||||||
| chr10:118698550
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.796+2756C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698550 | ||||||
| chr10:118698624
|
A | C | 47 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(44): Show | 52 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.796+2682T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698624 | ||||||
| chr10:118698654
|
C | A | 5 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(2): Show | 5 | HG00609.hp2 HG01074.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.796+2652G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698654 | ||||||
| chr10:118698919
|
T | TG | 258 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.796+2386_796+2387i others(3): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118698919 | ||||||
| chr10:118699003
|
T | G | 1 | a0001c0001t0009g0093 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.796+2303A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699003 | ||||||
| chr10:118699122
|
C | T | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.796+2184G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699122 | ||||||
| chr10:118699123
|
A | G | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.796+2183T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699123 | ||||||
| chr10:118699151
|
A | T | 22 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(19): Show | 23 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.796+2155T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699151 | ||||||
| chr10:118699649
|
A | AT | 240 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(237): Show | 264 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.796+1656dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699649 | ||||||
| chr10:118699649
|
A | ATT | 5 | a0001c0001t0002g0029a0001c0001t0013g0194a0001c0001t0031g0050others(2): Show | 6 | HG02257.hp2 HG02895.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.796+1655_796+1656d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699649 | ||||||
| chr10:118699693
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.796+1613C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699693 | ||||||
| chr10:118699745
|
C | T | 2 | a0001c0001t0030g0051a0001c0001t0030g0052 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.796+1561G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699745 | ||||||
| chr10:118699781
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.796+1525C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699781 | ||||||
| chr10:118699884
|
G | A | 1 | a0001c0001t0010g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.796+1422C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699884 | ||||||
| chr10:118699911
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.796+1395C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699911 | ||||||
| chr10:118699928
|
G | C | 1 | a0001c0001t0002g0331 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.796+1378C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699928 | ||||||
| chr10:118699969
|
G | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(240): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.796+1337C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118699969 | ||||||
| chr10:118700049
|
G | GA | 5 | a0001c0001t0006g0124a0001c0001t0021g0243a0001c0001t0063g0126others(2): Show | 5 | HG00438.hp1 HG02486.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.796+1256dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700049 | ||||||
| chr10:118700058
|
A | C | 85 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(82): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.796+1248T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700058 | ||||||
| chr10:118700298
|
A | G | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.796+1008T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700298 | ||||||
| chr10:118700304
|
G | A | 4 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0083g0342others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+1002C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700304 | ||||||
| chr10:118700447
|
G | C | 1 | a0001c0001t0079g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.796+859C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700447 | ||||||
| chr10:118700456
|
G | A | 2 | a0001c0001t0004g0075a0001c0001t0084g0343 | 2 | HG02559.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.796+850C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700456 | ||||||
| chr10:118700704
|
G | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.796+602C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700704 | ||||||
| chr10:118700716
|
C | CA | 14 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0079others(11): Show | 19 | HG02074.hp1 HG02145.hp1 HG02896.hp1 others(16): Show |
intron_variant | MODIFIER | c.796+589dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAA | 9 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(6): Show | 11 | HG01081.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.796+587_796+589dup others(3): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAA | 46 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(43): Show | 53 | HG00423.hp2 HG00673.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.796+586_796+589dup others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAA | 24 | a0001c0001t0003g0164a0001c0001t0003g0168a0001c0001t0003g0177others(21): Show | 27 | HG00438.hp2 HG00544.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.796+585_796+589dup others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0061g0049a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02451.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.796+578_796+589dup others(12): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0091g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.796+577_796+589dup others(13): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0030g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.796+574_796+589dup others(16): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0030g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.796+573_796+589dup others(17): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0031g0050a0001c0001t0031g0053 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.796+572_796+589dup others(18): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0051g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.796+571_796+589dup others(19): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700716
|
CAAAAAAA others(2): Show |
C | 153 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(150): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.796+581_796+589del others(9): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700716 | ||||||
| chr10:118700735
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02523.hp2 NA18975.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.796+571T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700735 | ||||||
| chr10:118700736
|
G | A | 9 | a0001c0001t0003g0183a0001c0001t0003g0184a0001c0001t0003g0186others(6): Show | 9 | HG02083.hp2 NA18950.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+570C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700736 | ||||||
| chr10:118700868
|
T | G | 5 | a0001c0001t0008g0009a0001c0001t0008g0044a0001c0001t0008g0046others(2): Show | 6 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.796+438A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700868 | ||||||
| chr10:118700951
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(241): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.796+355T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118700951 | ||||||
| chr10:118701203
|
G | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(153): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.796+103C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118701203 | ||||||
| chr10:118701220
|
C | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.796+86G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 5/8 | chr10 | 118701220 | ||||||
| chr10:118701801
|
C | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(240): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.694-393G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118701801 | ||||||
| chr10:118701926
|
G | A | 1 | a0001c0001t0006g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.694-518C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118701926 | ||||||
| chr10:118701927
|
G | A | 1 | a0001c0001t0006g0133 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.694-519C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118701927 | ||||||
| chr10:118702166
|
C | T | 1 | a0001c0001t0077g0031 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.694-758G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702166 | ||||||
| chr10:118702182
|
C | T | 1 | a0001c0001t0011g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.694-774G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702182 | ||||||
| chr10:118702235
|
C | G | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.694-827G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702235 | ||||||
| chr10:118702236
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.694-828A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702236 | ||||||
| chr10:118702443
|
G | C | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.694-1035C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702443 | ||||||
| chr10:118702584
|
CT | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(253): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.694-1177delA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702584 | ||||||
| chr10:118702644
|
C | T | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.694-1236G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702644 | ||||||
| chr10:118702645
|
G | A | 68 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.694-1237C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702645 | ||||||
| chr10:118702791
|
A | C | 1 | a0001c0001t0029g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.694-1383T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702791 | ||||||
| chr10:118702824
|
C | A | 1 | a0001c0001t0005g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.694-1416G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702824 | ||||||
| chr10:118702867
|
C | T | 11 | a0001c0001t0001g0023a0001c0001t0001g0214a0001c0001t0001g0236others(8): Show | 12 | HG00140.hp1 HG01070.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.694-1459G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702867 | ||||||
| chr10:118702975
|
T | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.694-1567A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118702975 | ||||||
| chr10:118703193
|
G | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.694-1785C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118703193 | ||||||
| chr10:118703247
|
TG | T | 68 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.694-1840delC | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118703247 | ||||||
| chr10:118703455
|
T | C | 1 | a0001c0001t0082g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.694-2047A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118703455 | ||||||
| chr10:118703553
|
T | C | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.694-2145A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118703553 | ||||||
| chr10:118703651
|
C | T | 1 | a0001c0001t0005g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.694-2243G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118703651 | ||||||
| chr10:118703964
|
AT | A | 14 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(11): Show | 16 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-2557delA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118703964 | ||||||
| chr10:118704081
|
T | TA | 15 | a0001c0001t0003g0170a0001c0002t0012g0037a0001c0002t0012g0057others(12): Show | 16 | HG00735.hp1 HG01081.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-2674dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704081 | ||||||
| chr10:118704091
|
G | C | 68 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.694-2683C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704091 | ||||||
| chr10:118704208
|
G | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.694-2800C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704208 | ||||||
| chr10:118704251
|
A | G | 68 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.694-2843T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704251 | ||||||
| chr10:118704492
|
C | G | 1 | a0001c0001t0006g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.693+3000G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704492 | ||||||
| chr10:118704699
|
A | G | 2 | a0001c0001t0044g0225a0001c0001t0045g0212 | 2 | NA18984.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.693+2793T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704699 | ||||||
| chr10:118704963
|
G | A | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.693+2529C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704963 | ||||||
| chr10:118704964
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.693+2528C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118704964 | ||||||
| chr10:118705274
|
A | C | 1 | a0001c0001t0001g0266 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.693+2218T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705274 | ||||||
| chr10:118705310
|
T | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(153): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.693+2182A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705310 | ||||||
| chr10:118705469
|
C | T | 2 | a0001c0001t0018g0140a0001c0001t0018g0148 | 2 | HG00735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.693+2023G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705469 | ||||||
| chr10:118705594
|
T | C | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.693+1898A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705594 | ||||||
| chr10:118705622
|
G | T | 1 | a0001c0001t0001g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.693+1870C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705622 | ||||||
| chr10:118705694
|
T | C | 14 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(11): Show | 16 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+1798A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705694 | ||||||
| chr10:118705776
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.693+1716A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118705776 | ||||||
| chr10:118706207
|
C | T | 1 | a0001c0001t0096g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.693+1285G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706207 | ||||||
| chr10:118706284
|
C | G | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.693+1208G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706284 | ||||||
| chr10:118706347
|
C | G | 1 | a0001c0001t0019g0255 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.693+1145G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706347 | ||||||
| chr10:118706421
|
A | C | 4 | a0001c0001t0018g0142a0001c0001t0018g0145a0001c0001t0018g0146others(1): Show | 4 | HG01081.hp2 HG02602.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+1071T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706421 | ||||||
| chr10:118706610
|
A | C | 1 | a0001c0001t0004g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.693+882T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706610 | ||||||
| chr10:118706625
|
G | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(240): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.693+867C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706625 | ||||||
| chr10:118706862
|
C | T | 68 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.693+630G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706862 | ||||||
| chr10:118706985
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+507T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118706985 | ||||||
| chr10:118707044
|
A | C | 1 | a0001c0001t0005g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.693+448T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118707044 | ||||||
| chr10:118707134
|
G | T | 1 | a0001c0001t0004g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.693+358C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118707134 | ||||||
| chr10:118707144
|
G | A | 3 | a0001c0001t0091g0041a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.693+348C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118707144 | ||||||
| chr10:118707168
|
A | C | 1 | a0001c0001t0002g0306 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.693+324T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118707168 | ||||||
| chr10:118707428
|
C | T | 1 | a0001c0001t0002g0309 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.693+64G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 4/8 | chr10 | 118707428 | ||||||
| chr10:118707701
|
C | CA | 68 | a0001c0001t0002g0308a0001c0001t0003g0002a0001c0001t0003g0019others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.598-115dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707701 | ||||||
| chr10:118707701
|
C | CAAA | 7 | a0001c0001t0008g0010a0001c0001t0008g0045a0001c0001t0051g0048others(4): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-117_598-115dup others(3): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707701 | ||||||
| chr10:118707701
|
C | CAAAA | 9 | a0001c0001t0008g0009a0001c0001t0008g0044a0001c0001t0008g0046others(6): Show | 10 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-118_598-115dup others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707701 | ||||||
| chr10:118707718
|
G | C | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-131C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707718 | ||||||
| chr10:118707725
|
C | T | 1 | a0001c0001t0006g0105 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.598-138G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707725 | ||||||
| chr10:118707835
|
T | G | 14 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(11): Show | 16 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.598-248A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707835 | ||||||
| chr10:118707920
|
T | C | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-333A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707920 | ||||||
| chr10:118707962
|
A | G | 1 | a0001c0001t0085g0197 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.598-375T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118707962 | ||||||
| chr10:118708009
|
G | C | 1 | a0001c0001t0059g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.598-422C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708009 | ||||||
| chr10:118708135
|
G | A | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 50 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.598-548C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708135 | ||||||
| chr10:118708147
|
C | CA | 87 | a0001c0001t0001g0026a0001c0001t0001g0207a0001c0001t0001g0224others(84): Show | 94 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.598-561dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708147 | ||||||
| chr10:118708147
|
C | CAA | 143 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(140): Show | 161 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.598-562_598-561dup others(2): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708147 | ||||||
| chr10:118708147
|
C | CAAA | 12 | a0001c0001t0001g0270a0001c0001t0001g0273a0001c0001t0001g0294others(9): Show | 12 | HG00423.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-563_598-561dup others(3): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708147 | ||||||
| chr10:118708147
|
CA | C | 19 | a0001c0001t0004g0065a0001c0001t0004g0113a0001c0001t0006g0104others(16): Show | 20 | HG00735.hp1 HG01081.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-561delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708147 | ||||||
| chr10:118708378
|
C | CA | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-792_598-791ins others(1): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708378 | ||||||
| chr10:118708719
|
C | T | 2 | a0001c0001t0002g0318a0001c0001t0002g0329 | 2 | NA18747.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.598-1132G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708719 | ||||||
| chr10:118708726
|
G | GT | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-1140dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708726 | ||||||
| chr10:118708933
|
G | A | 2 | a0001c0001t0003g0161a0001c0001t0014g0162 | 2 | NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.598-1346C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708933 | ||||||
| chr10:118708948
|
C | G | 1 | a0001c0001t0079g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598-1361G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118708948 | ||||||
| chr10:118709020
|
C | A | 1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.598-1433G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709020 | ||||||
| chr10:118709110
|
AAAGT | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0045 | 3 | HG02559.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.598-1527_598-1524d others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709110 | ||||||
| chr10:118709263
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.598-1676C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709263 | ||||||
| chr10:118709426
|
A | G | 1 | a0001c0001t0080g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.598-1839T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709426 | ||||||
| chr10:118709609
|
A | C | 1 | a0001c0001t0004g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.598-2022T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709609 | ||||||
| chr10:118709683
|
T | C | 1 | a0001c0001t0002g0338 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.598-2096A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709683 | ||||||
| chr10:118709845
|
G | A | 68 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(65): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.598-2258C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709845 | ||||||
| chr10:118709909
|
T | A | 8 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(5): Show | 8 | HG01192.hp2 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-2322A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709909 | ||||||
| chr10:118709937
|
G | C | 1 | a0001c0001t0030g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.598-2350C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118709937 | ||||||
| chr10:118710005
|
A | G | 1 | a0001c0001t0032g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.598-2418T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710005 | ||||||
| chr10:118710070
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | NA18985.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.598-2483C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710070 | ||||||
| chr10:118710084
|
T | C | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-2497A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710084 | ||||||
| chr10:118710088
|
G | C | 1 | a0001c0002t0012g0059 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.598-2501C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710088 | ||||||
| chr10:118710090
|
A | AT | 26 | a0001c0001t0001g0236a0001c0001t0001g0272a0001c0001t0001g0327others(23): Show | 28 | HG00140.hp1 HG01175.hp1 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.598-2504dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710090 | ||||||
| chr10:118710090
|
A | ATT | 71 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(68): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.598-2505_598-2504d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710090 | ||||||
| chr10:118710090
|
AT | A | 8 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0249others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-2504delA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710090 | ||||||
| chr10:118710208
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(107): Show | 119 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.598-2621C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710208 | ||||||
| chr10:118710225
|
G | C | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-2638C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710225 | ||||||
| chr10:118710334
|
G | A | 2 | a0001c0001t0030g0051a0001c0001t0030g0052 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.598-2747C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710334 | ||||||
| chr10:118710367
|
T | G | 13 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(10): Show | 14 | HG00735.hp1 HG01081.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.598-2780A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710367 | ||||||
| chr10:118710537
|
G | A | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-2950C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710537 | ||||||
| chr10:118710737
|
A | G | 12 | a0001c0001t0015g0020a0001c0001t0015g0141a0001c0001t0015g0144others(9): Show | 13 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.598-3150T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710737 | ||||||
| chr10:118710787
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0338 | 3 | HG03490.hp1 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.598-3200C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710787 | ||||||
| chr10:118710863
|
T | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.598-3276A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118710863 | ||||||
| chr10:118711366
|
C | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.598-3779G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118711366 | ||||||
| chr10:118711370
|
G | A | 1 | a0002c0006t0004g0345 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.598-3783C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118711370 | ||||||
| chr10:118711482
|
C | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(240): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.598-3895G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118711482 | ||||||
| chr10:118711645
|
T | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.598-4058A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118711645 | ||||||
| chr10:118711913
|
G | GA | 24 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(21): Show | 25 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-4327dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118711913 | ||||||
| chr10:118712089
|
A | C | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-4502T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712089 | ||||||
| chr10:118712242
|
G | A | 24 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(21): Show | 25 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-4655C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712242 | ||||||
| chr10:118712296
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598-4709C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712296 | ||||||
| chr10:118712323
|
C | T | 72 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(69): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.598-4736G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712323 | ||||||
| chr10:118712407
|
G | T | 1 | a0001c0001t0004g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.598-4820C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712407 | ||||||
| chr10:118712437
|
G | T | 2 | a0001c0001t0007g0335a0001c0001t0007g0337 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.598-4850C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712437 | ||||||
| chr10:118712752
|
C | T | 3 | a0001c0001t0026g0217a0001c0001t0026g0218a0001c0001t0026g0235 | 3 | HG04228.hp1 NA18991.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.598-5165G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712752 | ||||||
| chr10:118712835
|
C | T | 1 | a0001c0001t0089g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.598-5248G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712835 | ||||||
| chr10:118712939
|
T | G | 3 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0310 | 3 | HG01106.hp2 HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.598-5352A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118712939 | ||||||
| chr10:118713085
|
T | C | 87 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(84): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-5498A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713085 | ||||||
| chr10:118713172
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.598-5585C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713172 | ||||||
| chr10:118713217
|
C | T | 1 | a0001c0001t0086g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.598-5630G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713217 | ||||||
| chr10:118713351
|
T | C | 1 | a0001c0001t0013g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.598-5764A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713351 | ||||||
| chr10:118713485
|
C | T | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0079others(5): Show | 11 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.598-5898G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713485 | ||||||
| chr10:118713489
|
TGG | T | 5 | a0001c0001t0008g0009a0001c0001t0008g0044a0001c0001t0008g0046others(2): Show | 6 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-5904_598-5903d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713489 | ||||||
| chr10:118713510
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.598-5923T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713510 | ||||||
| chr10:118713903
|
A | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.598-6316T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118713903 | ||||||
| chr10:118714131
|
C | T | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598-6544G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714131 | ||||||
| chr10:118714233
|
G | A | 1 | a0001c0001t0087g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.598-6646C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714233 | ||||||
| chr10:118714522
|
A | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.598-6935T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714522 | ||||||
| chr10:118714534
|
G | T | 256 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(253): Show | 281 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.598-6947C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714534 | ||||||
| chr10:118714611
|
T | A | 73 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(70): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.598-7024A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714611 | ||||||
| chr10:118714726
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.598-7139G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714726 | ||||||
| chr10:118714791
|
C | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0079g0206 | 3 | HG02895.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.598-7204G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714791 | ||||||
| chr10:118714840
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.598-7253C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714840 | ||||||
| chr10:118714843
|
T | C | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.598-7256A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118714843 | ||||||
| chr10:118715114
|
G | A | 1 | a0001c0001t0103g0143 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.598-7527C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715114 | ||||||
| chr10:118715243
|
T | C | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598-7656A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715243 | ||||||
| chr10:118715339
|
A | C | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598-7752T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715339 | ||||||
| chr10:118715426
|
T | C | 10 | a0001c0001t0002g0028a0001c0001t0004g0127a0001c0001t0004g0128others(7): Show | 12 | HG00140.hp2 HG01361.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.598-7839A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715426 | ||||||
| chr10:118715502
|
T | C | 1 | a0001c0001t0103g0143 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.598-7915A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715502 | ||||||
| chr10:118715533
|
A | G | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 49 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-7946T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715533 | ||||||
| chr10:118715552
|
T | C | 3 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0046g0154 | 3 | HG01192.hp2 HG01891.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.598-7965A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715552 | ||||||
| chr10:118715667
|
C | T | 3 | a0001c0001t0091g0041a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598-8080G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715667 | ||||||
| chr10:118715726
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.598-8139C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715726 | ||||||
| chr10:118715835
|
G | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0219a0001c0001t0001g0221others(2): Show | 5 | HG02809.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-8248C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715835 | ||||||
| chr10:118715965
|
G | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.598-8378C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118715965 | ||||||
| chr10:118716018
|
C | T | 1 | a0001c0001t0046g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.598-8431G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716018 | ||||||
| chr10:118716048
|
C | T | 1 | a0001c0001t0027g0188 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.598-8461G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716048 | ||||||
| chr10:118716058
|
C | T | 1 | a0001c0001t0005g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-8471G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716058 | ||||||
| chr10:118716102
|
C | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(239): Show | 266 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.598-8515G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716102 | ||||||
| chr10:118716305
|
AT | A | 85 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(82): Show | 94 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.598-8719delA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716305 | ||||||
| chr10:118716305
|
ATT | A | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 49 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-8720_598-8719d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716305 | ||||||
| chr10:118716398
|
C | T | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-8811G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716398 | ||||||
| chr10:118716411
|
G | A | 1 | a0001c0001t0015g0144 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.598-8824C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716411 | ||||||
| chr10:118716480
|
T | G | 24 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(21): Show | 25 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-8893A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716480 | ||||||
| chr10:118716605
|
C | CTT | 151 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(148): Show | 164 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.598-9020_598-9019d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716605 | ||||||
| chr10:118716631
|
C | T | 1 | a0001c0001t0080g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.598-9044G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716631 | ||||||
| chr10:118716691
|
T | C | 1 | a0001c0001t0079g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598-9104A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716691 | ||||||
| chr10:118716785
|
C | G | 69 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(66): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.598-9198G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716785 | ||||||
| chr10:118716785
|
C | T | 1 | a0001c0001t0004g0113 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.598-9198G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716785 | ||||||
| chr10:118716792
|
C | T | 8 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(5): Show | 10 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-9205G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716792 | ||||||
| chr10:118716835
|
T | A | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-9248A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716835 | ||||||
| chr10:118716887
|
C | T | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0079others(5): Show | 11 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.598-9300G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716887 | ||||||
| chr10:118716985
|
C | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.598-9398G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118716985 | ||||||
| chr10:118717239
|
A | C | 1 | a0001c0001t0024g0234 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.598-9652T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118717239 | ||||||
| chr10:118717478
|
A | G | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 49 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-9891T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118717478 | ||||||
| chr10:118717883
|
C | T | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-10296G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118717883 | ||||||
| chr10:118717954
|
CA | C | 70 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(67): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.598-10368delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118717954 | ||||||
| chr10:118717955
|
A | G | 1 | a0001c0002t0034g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.598-10368T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118717955 | ||||||
| chr10:118718110
|
G | C | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-10523C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718110 | ||||||
| chr10:118718258
|
G | C | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-10671C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718258 | ||||||
| chr10:118718340
|
A | G | 228 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(225): Show | 250 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.598-10753T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718340 | ||||||
| chr10:118718352
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.598-10765C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718352 | ||||||
| chr10:118718466
|
C | T | 69 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(66): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.597+10829G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718466 | ||||||
| chr10:118718470
|
T | C | 16 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(13): Show | 18 | HG01175.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.597+10825A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718470 | ||||||
| chr10:118718541
|
T | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(253): Show | 281 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.597+10754A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718541 | ||||||
| chr10:118718550
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(152): Show | 168 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.597+10745C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718550 | ||||||
| chr10:118718573
|
A | G | 5 | a0001c0001t0002g0303a0001c0001t0002g0315a0001c0001t0002g0318others(2): Show | 5 | NA18747.hp2 NA18957.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+10722T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718573 | ||||||
| chr10:118718583
|
C | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(225): Show | 250 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.597+10712G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718583 | ||||||
| chr10:118718676
|
C | T | 69 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(66): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.597+10619G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718676 | ||||||
| chr10:118718764
|
G | A | 2 | a0001c0001t0030g0051a0001c0001t0030g0052 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.597+10531C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718764 | ||||||
| chr10:118718767
|
T | G | 73 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(70): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.597+10528A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718767 | ||||||
| chr10:118718808
|
C | T | 2 | a0001c0002t0012g0059a0001c0002t0034g0058 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.597+10487G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718808 | ||||||
| chr10:118718835
|
A | G | 14 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(11): Show | 15 | HG00735.hp1 HG01081.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+10460T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718835 | ||||||
| chr10:118718862
|
C | T | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+10433G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118718862 | ||||||
| chr10:118719238
|
T | C | 1 | a0001c0001t0079g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.597+10057A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719238 | ||||||
| chr10:118719248
|
G | A | 5 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0155others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+10047C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719248 | ||||||
| chr10:118719413
|
T | C | 3 | a0001c0001t0004g0070a0001c0001t0056g0068a0001c0005t0004g0069 | 3 | HG00323.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.597+9882A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719413 | ||||||
| chr10:118719627
|
C | T | 2 | a0001c0001t0001g0223a0001c0004t0001g0030 | 2 | NA18956.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.597+9668G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719627 | ||||||
| chr10:118719641
|
G | A | 4 | a0001c0002t0012g0037a0001c0002t0012g0059a0001c0002t0034g0058others(1): Show | 5 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+9654C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719641 | ||||||
| chr10:118719827
|
A | G | 1 | a0001c0001t0096g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597+9468T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719827 | ||||||
| chr10:118719855
|
T | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.597+9440A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719855 | ||||||
| chr10:118719925
|
T | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.597+9370A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118719925 | ||||||
| chr10:118720395
|
C | T | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.597+8900G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720395 | ||||||
| chr10:118720451
|
C | A | 1 | a0001c0001t0098g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.597+8844G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720451 | ||||||
| chr10:118720519
|
TTGTACTC others(15): Show |
T | 2 | a0001c0001t0003g0161a0001c0001t0014g0162 | 2 | NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.597+8754_597+8775d others(24): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720519 | ||||||
| chr10:118720651
|
T | C | 46 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(43): Show | 51 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.597+8644A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720651 | ||||||
| chr10:118720670
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.597+8625T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720670 | ||||||
| chr10:118720748
|
A | G | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.597+8547T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720748 | ||||||
| chr10:118720853
|
G | T | 1 | a0001c0001t0038g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.597+8442C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720853 | ||||||
| chr10:118720923
|
T | C | 1 | a0001c0005t0004g0069 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.597+8372A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118720923 | ||||||
| chr10:118721001
|
T | C | 1 | a0001c0001t0002g0333 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.597+8294A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721001 | ||||||
| chr10:118721171
|
T | A | 46 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(43): Show | 51 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.597+8124A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721171 | ||||||
| chr10:118721174
|
C | T | 3 | a0001c0001t0002g0203a0001c0001t0007g0301a0001c0001t0007g0314 | 3 | NA18959.hp2 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.597+8121G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721174 | ||||||
| chr10:118721176
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(107): Show | 119 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.597+8119C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721176 | ||||||
| chr10:118721235
|
C | T | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+8060G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721235 | ||||||
| chr10:118721458
|
AATTTT | A | 5 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0309others(2): Show | 5 | HG01106.hp2 HG01123.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+7832_597+7836d others(7): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721458 | ||||||
| chr10:118721480
|
T | C | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+7815A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721480 | ||||||
| chr10:118721550
|
G | C | 6 | a0001c0001t0013g0006a0001c0001t0013g0179a0001c0001t0013g0194others(3): Show | 8 | HG00544.hp1 NA18612.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+7745C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721550 | ||||||
| chr10:118721620
|
T | C | 1 | a0001c0001t0010g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.597+7675A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721620 | ||||||
| chr10:118721634
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.597+7661C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721634 | ||||||
| chr10:118721641
|
T | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(240): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.597+7654A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721641 | ||||||
| chr10:118721712
|
G | A | 24 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(21): Show | 25 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.597+7583C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721712 | ||||||
| chr10:118721821
|
C | A | 69 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(66): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.597+7474G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721821 | ||||||
| chr10:118721866
|
C | T | 2 | a0001c0001t0003g0170a0001c0001t0014g0169 | 2 | NA18967.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.597+7429G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721866 | ||||||
| chr10:118721917
|
T | C | 1 | a0001c0001t0026g0218 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.597+7378A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118721917 | ||||||
| chr10:118722080
|
CT | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(160): Show | 181 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.597+7214delA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722080 | ||||||
| chr10:118722152
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(98): Show | 110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.597+7143G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722152 | ||||||
| chr10:118722178
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328 | 3 | HG01074.hp2 HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.597+7117C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722178 | ||||||
| chr10:118722433
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.597+6862G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722433 | ||||||
| chr10:118722533
|
T | C | 1 | a0001c0001t0038g0211 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.597+6762A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722533 | ||||||
| chr10:118722565
|
C | T | 1 | a0001c0001t0005g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597+6730G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722565 | ||||||
| chr10:118722656
|
C | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+6639G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722656 | ||||||
| chr10:118722800
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0286 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.597+6495C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722800 | ||||||
| chr10:118722986
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.597+6309C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118722986 | ||||||
| chr10:118723095
|
G | T | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.597+6200C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723095 | ||||||
| chr10:118723097
|
A | ACATT | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.597+6197_597+6198i others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723097 | ||||||
| chr10:118723421
|
T | C | 86 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.597+5874A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723421 | ||||||
| chr10:118723516
|
T | C | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.597+5779A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723516 | ||||||
| chr10:118723626
|
C | T | 1 | a0001c0001t0002g0028 | 2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.597+5669G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723626 | ||||||
| chr10:118723859
|
G | A | 43 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(40): Show | 51 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.597+5436C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723859 | ||||||
| chr10:118723910
|
G | GC | 11 | a0001c0002t0012g0057a0001c0002t0012g0059a0001c0002t0012g0061others(8): Show | 11 | HG00735.hp1 HG01081.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+5384dupG | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723910 | ||||||
| chr10:118723923
|
C | G | 1 | a0001c0001t0018g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.597+5372G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723923 | ||||||
| chr10:118723928
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0280a0001c0001t0001g0281others(4): Show | 8 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+5367C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118723928 | ||||||
| chr10:118724045
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0019g0298 | 3 | HG02280.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.597+5250T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724045 | ||||||
| chr10:118724260
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.597+5035T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724260 | ||||||
| chr10:118724376
|
A | AT | 13 | a0001c0001t0001g0021a0001c0001t0001g0204a0001c0001t0001g0229others(10): Show | 15 | HG02165.hp1 HG03704.hp2 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+4918dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724376 | ||||||
| chr10:118724592
|
T | C | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+4703A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724592 | ||||||
| chr10:118724614
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.597+4681A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724614 | ||||||
| chr10:118724638
|
T | C | 1 | a0001c0001t0005g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.597+4657A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724638 | ||||||
| chr10:118724710
|
A | G | 2 | a0001c0001t0007g0335a0001c0001t0007g0337 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.597+4585T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724710 | ||||||
| chr10:118724714
|
T | C | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.597+4581A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118724714 | ||||||
| chr10:118725232
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(99): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.597+4063G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725232 | ||||||
| chr10:118725323
|
C | T | 1 | a0001c0001t0002g0340 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.597+3972G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725323 | ||||||
| chr10:118725375
|
G | A | 8 | a0001c0001t0001g0223a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | NA18947.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+3920C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725375 | ||||||
| chr10:118725412
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG00423.hp1 HG02027.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+3883C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725412 | ||||||
| chr10:118725437
|
T | C | 88 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(85): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.597+3858A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725437 | ||||||
| chr10:118725586
|
G | A | 26 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(23): Show | 27 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.597+3709C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725586 | ||||||
| chr10:118725712
|
T | C | 3 | a0001c0001t0091g0041a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.597+3583A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725712 | ||||||
| chr10:118725754
|
G | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(153): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.597+3541C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725754 | ||||||
| chr10:118725802
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597+3493T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725802 | ||||||
| chr10:118725887
|
A | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.597+3408T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725887 | ||||||
| chr10:118725909
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(88): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.597+3386A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725909 | ||||||
| chr10:118725992
|
C | T | 2 | a0001c0001t0001g0273a0001c0001t0051g0048 | 2 | HG02257.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.597+3303G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118725992 | ||||||
| chr10:118726002
|
G | A | 1 | a0001c0001t0097g0222 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.597+3293C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726002 | ||||||
| chr10:118726094
|
CAAT | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.597+3198_597+3200d others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726094 | ||||||
| chr10:118726389
|
T | C | 13 | a0001c0001t0031g0053a0001c0002t0012g0037a0001c0002t0012g0057others(10): Show | 14 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.597+2906A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726389 | ||||||
| chr10:118726445
|
C | G | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+2850G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726445 | ||||||
| chr10:118726511
|
T | C | 1 | a0001c0001t0004g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.597+2784A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726511 | ||||||
| chr10:118726512
|
A | G | 88 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(85): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.597+2783T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726512 | ||||||
| chr10:118726515
|
C | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.597+2780G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726515 | ||||||
| chr10:118726582
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(99): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.597+2713C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726582 | ||||||
| chr10:118726677
|
G | A | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.597+2618C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726677 | ||||||
| chr10:118726763
|
C | T | 1 | a0001c0001t0005g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.597+2532G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726763 | ||||||
| chr10:118726846
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+2449C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726846 | ||||||
| chr10:118726900
|
C | A | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.597+2395G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118726900 | ||||||
| chr10:118727071
|
T | C | 14 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(11): Show | 16 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+2224A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727071 | ||||||
| chr10:118727077
|
A | G | 1 | a0001c0001t0007g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.597+2218T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727077 | ||||||
| chr10:118727141
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.597+2154A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727141 | ||||||
| chr10:118727155
|
G | A | 1 | a0001c0001t0047g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.597+2140C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727155 | ||||||
| chr10:118727206
|
C | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.597+2089G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727206 | ||||||
| chr10:118727357
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.597+1938C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727357 | ||||||
| chr10:118727403
|
T | A | 1 | a0001c0001t0014g0162 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.597+1892A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727403 | ||||||
| chr10:118727403
|
T | TA | 188 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(185): Show | 207 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.597+1891dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727403 | ||||||
| chr10:118727403
|
T | TAA | 46 | a0001c0001t0001g0265a0001c0001t0001g0316a0001c0001t0001g0327others(43): Show | 51 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.597+1890_597+1891d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727403 | ||||||
| chr10:118727403
|
T | TAAA | 22 | a0001c0001t0002g0306a0001c0001t0002g0329a0001c0001t0002g0330others(19): Show | 24 | HG01109.hp2 HG02135.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.597+1889_597+1891d others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727403 | ||||||
| chr10:118727480
|
A | G | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.597+1815T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727480 | ||||||
| chr10:118727639
|
G | A | 1 | a0001c0001t0101g0341 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.597+1656C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118727639 | ||||||
| chr10:118728090
|
ACAG | A | 26 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(23): Show | 27 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.597+1202_597+1204d others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728090 | ||||||
| chr10:118728139
|
C | A | 1 | a0001c0001t0040g0014 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.597+1156G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728139 | ||||||
| chr10:118728234
|
T | C | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.597+1061A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728234 | ||||||
| chr10:118728317
|
C | CT | 211 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(208): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.597+977dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728317 | ||||||
| chr10:118728317
|
C | CTT | 8 | a0001c0001t0002g0315a0001c0001t0003g0163a0001c0001t0003g0164others(5): Show | 8 | HG02109.hp2 NA18942.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+976_597+977dup others(2): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728317 | ||||||
| chr10:118728382
|
C | T | 1 | a0001c0001t0050g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.597+913G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728382 | ||||||
| chr10:118728531
|
T | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(243): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.597+764A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728531 | ||||||
| chr10:118728814
|
C | G | 1 | a0001c0001t0003g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.597+481G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728814 | ||||||
| chr10:118728940
|
C | T | 1 | a0001c0001t0002g0028 | 2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.597+355G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118728940 | ||||||
| chr10:118729113
|
C | T | 5 | a0001c0002t0012g0061a0001c0002t0020g0055a0001c0002t0020g0056others(2): Show | 5 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+182G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118729113 | ||||||
| chr10:118729120
|
T | C | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+175A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118729120 | ||||||
| chr10:118729162
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.597+133G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 3/8 | chr10 | 118729162 | ||||||
| chr10:118729555
|
C | T | 1 | a0001c0001t0019g0263 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.495-158G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 2/8 | chr10 | 118729555 | ||||||
| chr10:118729782
|
C | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.495-385G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 2/8 | chr10 | 118729782 | ||||||
| chr10:118729882
|
T | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0204a0001c0001t0001g0248others(3): Show | 7 | HG02040.hp1 HG02165.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.494+402A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 2/8 | chr10 | 118729882 | ||||||
| chr10:118729948
|
G | A | 1 | a0001c0001t0018g0145 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.494+336C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 2/8 | chr10 | 118729948 | ||||||
| chr10:118730033
|
T | C | 44 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(41): Show | 47 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.494+251A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 2/8 | chr10 | 118730033 | ||||||
| chr10:118730556
|
A | C | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368-146T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730556 | ||||||
| chr10:118730583
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368-173C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730583 | ||||||
| chr10:118730668
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0079others(5): Show | 11 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.368-258T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730668 | ||||||
| chr10:118730772
|
G | A | 1 | a0002c0006t0004g0345 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.368-362C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730772 | ||||||
| chr10:118730844
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.368-434C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730844 | ||||||
| chr10:118730878
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(154): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.368-468A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730878 | ||||||
| chr10:118730884
|
C | A | 1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.368-474G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118730884 | ||||||
| chr10:118731170
|
A | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0224a0001c0001t0001g0228others(12): Show | 18 | HG00544.hp2 HG00673.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.368-760T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731170 | ||||||
| chr10:118731275
|
T | C | 1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.368-865A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731275 | ||||||
| chr10:118731387
|
C | T | 2 | a0001c0001t0036g0078a0001c0001t0040g0014 | 3 | HG01884.hp1 HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.368-977G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731387 | ||||||
| chr10:118731388
|
G | A | 2 | a0001c0001t0001g0339a0001c0001t0078g0332 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.368-978C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731388 | ||||||
| chr10:118731835
|
T | C | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.368-1425A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731835 | ||||||
| chr10:118731994
|
C | T | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 50 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-1584G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731994 | ||||||
| chr10:118731998
|
C | T | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.368-1588G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118731998 | ||||||
| chr10:118732048
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368-1638A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118732048 | ||||||
| chr10:118732162
|
G | C | 1 | a0001c0001t0004g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.368-1752C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118732162 | ||||||
| chr10:118732477
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368-2067A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118732477 | ||||||
| chr10:118732512
|
G | A | 45 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(42): Show | 53 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.368-2102C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118732512 | ||||||
| chr10:118732944
|
T | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.368-2534A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118732944 | ||||||
| chr10:118732946
|
C | T | 2 | a0001c0001t0029g0103a0001c0001t0029g0115 | 2 | NA18942.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.368-2536G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118732946 | ||||||
| chr10:118733091
|
G | A | 1 | a0001c0001t0080g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.368-2681C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733091 | ||||||
| chr10:118733111
|
A | G | 1 | a0001c0001t0010g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.368-2701T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733111 | ||||||
| chr10:118733290
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.368-2880T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733290 | ||||||
| chr10:118733332
|
A | C | 13 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(10): Show | 13 | HG02083.hp2 HG02109.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-2922T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733332 | ||||||
| chr10:118733356
|
A | G | 1 | a0001c0001t0007g0313 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.368-2946T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733356 | ||||||
| chr10:118733407
|
A | C | 1 | a0001c0001t0098g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.368-2997T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733407 | ||||||
| chr10:118733445
|
A | G | 1 | a0001c0001t0016g0011 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.368-3035T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733445 | ||||||
| chr10:118733485
|
G | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.368-3075C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733485 | ||||||
| chr10:118733487
|
C | T | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.368-3077G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733487 | ||||||
| chr10:118733488
|
A | AAATG | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.368-3079_368-3078i others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733488 | ||||||
| chr10:118733639
|
G | C | 1 | a0001c0001t0018g0148 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.368-3229C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733639 | ||||||
| chr10:118733738
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(144): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.368-3328C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733738 | ||||||
| chr10:118733783
|
G | A | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 50 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-3373C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733783 | ||||||
| chr10:118733856
|
TA | T | 342 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(339): Show | 385 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(382): Show |
intron_variant | MODIFIER | c.368-3447delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118733856 | ||||||
| chr10:118734110
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.368-3700G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734110 | ||||||
| chr10:118734168
|
C | T | 2 | a0001c0001t0030g0051a0001c0001t0030g0052 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.368-3758G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734168 | ||||||
| chr10:118734188
|
A | G | 156 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(153): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.368-3778T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734188 | ||||||
| chr10:118734269
|
T | C | 2 | a0001c0001t0031g0050a0001c0001t0031g0053 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.368-3859A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734269 | ||||||
| chr10:118734338
|
C | T | 12 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(9): Show | 13 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.368-3928G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734338 | ||||||
| chr10:118734493
|
T | A | 1 | a0001c0001t0002g0333 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.368-4083A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734493 | ||||||
| chr10:118734525
|
T | C | 2 | a0001c0001t0049g0138a0001c0001t0050g0137 | 2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.368-4115A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734525 | ||||||
| chr10:118734619
|
G | A | 2 | a0001c0001t0002g0312a0001c0001t0002g0334 | 2 | HG00609.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.368-4209C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734619 | ||||||
| chr10:118734839
|
T | G | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.368-4429A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734839 | ||||||
| chr10:118734860
|
T | C | 19 | a0001c0001t0006g0071a0001c0001t0006g0100a0001c0001t0006g0104others(16): Show | 19 | HG03710.hp1 HG03942.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.368-4450A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118734860 | ||||||
| chr10:118735194
|
T | G | 1 | a0001c0001t0002g0311 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.368-4784A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118735194 | ||||||
| chr10:118735271
|
T | C | 1 | a0001c0001t0061g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.368-4861A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118735271 | ||||||
| chr10:118735429
|
T | C | 1 | a0001c0001t0003g0198 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.368-5019A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118735429 | ||||||
| chr10:118735591
|
G | C | 1 | a0001c0001t0002g0306 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.368-5181C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118735591 | ||||||
| chr10:118735652
|
C | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.368-5242G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118735652 | ||||||
| chr10:118736161
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.368-5751A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736161 | ||||||
| chr10:118736260
|
T | C | 43 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(40): Show | 46 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.368-5850A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736260 | ||||||
| chr10:118736266
|
AG | A | 12 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(9): Show | 13 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.368-5857delC | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736266 | ||||||
| chr10:118736359
|
C | T | 9 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0004g0129others(6): Show | 10 | HG01361.hp2 HG01515.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-5949G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736359 | ||||||
| chr10:118736389
|
A | AT | 6 | a0001c0001t0004g0012a0001c0001t0004g0070a0001c0001t0004g0073others(3): Show | 7 | HG00323.hp1 HG01070.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-5980dupA | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736389 | ||||||
| chr10:118736492
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.368-6082G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736492 | ||||||
| chr10:118736499
|
A | G | 1 | a0001c0001t0002g0029 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.368-6089T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736499 | ||||||
| chr10:118736556
|
G | A | 1 | a0001c0001t0004g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.368-6146C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736556 | ||||||
| chr10:118736576
|
C | CA | 43 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(40): Show | 46 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.368-6167dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736576 | ||||||
| chr10:118736784
|
G | A | 1 | a0001c0001t0051g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.368-6374C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736784 | ||||||
| chr10:118736796
|
C | T | 1 | a0001c0001t0061g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.368-6386G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118736796 | ||||||
| chr10:118737134
|
G | GA | 28 | a0001c0001t0001g0260a0001c0001t0001g0265a0001c0001t0001g0273others(25): Show | 28 | HG02055.hp2 HG02071.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.368-6725dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737134 | ||||||
| chr10:118737134
|
GA | G | 10 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(7): Show | 11 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-6725delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737134 | ||||||
| chr10:118737135
|
A | G | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368-6725T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737135 | ||||||
| chr10:118737158
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.368-6748A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737158 | ||||||
| chr10:118737220
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.368-6810C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737220 | ||||||
| chr10:118737374
|
C | T | 1 | a0001c0001t0038g0211 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.368-6964G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737374 | ||||||
| chr10:118737481
|
C | T | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.368-7071G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737481 | ||||||
| chr10:118737533
|
T | C | 1 | a0001c0001t0061g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.368-7123A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737533 | ||||||
| chr10:118737669
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.368-7259G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737669 | ||||||
| chr10:118737689
|
TA | T | 246 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(243): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.368-7280delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737689 | ||||||
| chr10:118737851
|
C | T | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-7441G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118737851 | ||||||
| chr10:118738067
|
A | T | 88 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(85): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.368-7657T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738067 | ||||||
| chr10:118738180
|
G | A | 1 | a0001c0001t0014g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.368-7770C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738180 | ||||||
| chr10:118738224
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(98): Show | 110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.368-7814A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738224 | ||||||
| chr10:118738292
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(105): Show | 117 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.368-7882C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738292 | ||||||
| chr10:118738440
|
C | T | 88 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(85): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.368-8030G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738440 | ||||||
| chr10:118738766
|
T | A | 1 | a0001c0001t0002g0028 | 2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.368-8356A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738766 | ||||||
| chr10:118738858
|
CAG | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.368-8450_368-8449d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738858 | ||||||
| chr10:118738892
|
T | TA | 127 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(124): Show | 137 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.368-8483dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAA | 47 | a0001c0001t0001g0265a0001c0001t0003g0002a0001c0001t0003g0019others(44): Show | 55 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.368-8484_368-8483d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAAA | 14 | a0001c0001t0001g0260a0001c0001t0002g0307a0001c0001t0002g0308others(11): Show | 14 | HG00423.hp2 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.368-8485_368-8483d others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAAAA | 35 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(32): Show | 40 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.368-8486_368-8483d others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0031g0053 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.368-8495_368-8483d others(15): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAAAAAAA others(7): Show |
2 | a0001c0001t0031g0050a0001c0001t0061g0049 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.368-8496_368-8483d others(16): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAAAAAAA others(9): Show |
2 | a0001c0001t0091g0041a0001c0001t0098g0040 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.368-8498_368-8483d others(18): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
T | TAAAAAAA others(15): Show |
1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.368-8504_368-8483d others(24): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738892
|
TAA | T | 7 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(4): Show | 9 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.368-8484_368-8483d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738892 | ||||||
| chr10:118738935
|
C | T | 1 | a0001c0001t0018g0140 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.368-8525G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118738935 | ||||||
| chr10:118739065
|
G | A | 1 | a0001c0001t0019g0255 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.368-8655C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739065 | ||||||
| chr10:118739067
|
G | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0219a0001c0001t0001g0221others(2): Show | 5 | HG02809.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-8657C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739067 | ||||||
| chr10:118739088
|
C | T | 45 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(42): Show | 50 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-8678G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739088 | ||||||
| chr10:118739122
|
G | T | 1 | a0001c0001t0032g0072 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.368-8712C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739122 | ||||||
| chr10:118739193
|
TC | T | 3 | a0001c0001t0091g0041a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.368-8784delG | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739193 | ||||||
| chr10:118739194
|
CA | C | 84 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(81): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.368-8785delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739194 | ||||||
| chr10:118739195
|
A | T | 3 | a0001c0001t0091g0041a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.368-8785T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739195 | ||||||
| chr10:118739314
|
AC | A | 8 | a0001c0001t0001g0223a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | NA18947.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.368-8905delG | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739314 | ||||||
| chr10:118739391
|
A | G | 1 | a0001c0001t0061g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.368-8981T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739391 | ||||||
| chr10:118739396
|
A | G | 1 | a0001c0001t0002g0302 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.368-8986T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739396 | ||||||
| chr10:118739429
|
C | T | 2 | a0001c0001t0003g0161a0001c0001t0014g0162 | 2 | NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.368-9019G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739429 | ||||||
| chr10:118739868
|
G | C | 1 | a0001c0001t0004g0070 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.368-9458C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739868 | ||||||
| chr10:118739974
|
G | A | 26 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(23): Show | 27 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.368-9564C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739974 | ||||||
| chr10:118739981
|
C | T | 1 | a0001c0001t0051g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.368-9571G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118739981 | ||||||
| chr10:118740117
|
A | G | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.368-9707T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118740117 | ||||||
| chr10:118740134
|
G | A | 12 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(9): Show | 13 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.368-9724C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118740134 | ||||||
| chr10:118740630
|
T | A | 2 | a0001c0001t0007g0335a0001c0001t0007g0337 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.368-10220A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118740630 | ||||||
| chr10:118740842
|
C | T | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.368-10432G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118740842 | ||||||
| chr10:118740867
|
A | T | 71 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(68): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.368-10457T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118740867 | ||||||
| chr10:118740944
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368-10534G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118740944 | ||||||
| chr10:118741047
|
A | G | 1 | a0001c0001t0061g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.368-10637T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741047 | ||||||
| chr10:118741307
|
C | A | 2 | a0001c0001t0091g0041a0001c0001t0098g0040 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.368-10897G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741307 | ||||||
| chr10:118741465
|
G | GAC | 19 | a0001c0001t0001g0033a0001c0001t0005g0118a0001c0001t0008g0009others(16): Show | 21 | HG02129.hp1 HG02257.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.368-11057_368-1105 others(6): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741465 | ||||||
| chr10:118741484
|
C | A | 59 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(56): Show | 66 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.368-11074G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741484 | ||||||
| chr10:118741543
|
G | A | 1 | a0001c0001t0004g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.368-11133C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741543 | ||||||
| chr10:118741635
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.368-11225G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741635 | ||||||
| chr10:118741719
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.368-11309T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741719 | ||||||
| chr10:118741726
|
C | T | 2 | a0001c0001t0018g0140a0001c0001t0018g0148 | 2 | HG00735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.368-11316G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741726 | ||||||
| chr10:118741885
|
T | C | 1 | a0001c0001t0007g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.368-11475A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741885 | ||||||
| chr10:118741973
|
C | A | 1 | a0001c0001t0005g0119 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.368-11563G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118741973 | ||||||
| chr10:118742305
|
A | G | 1 | a0001c0001t0051g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.368-11895T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742305 | ||||||
| chr10:118742458
|
G | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.367+11938C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742458 | ||||||
| chr10:118742655
|
C | G | 14 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(11): Show | 16 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.367+11741G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742655 | ||||||
| chr10:118742796
|
C | T | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367+11600G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742796 | ||||||
| chr10:118742828
|
T | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG01070.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.367+11568A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742828 | ||||||
| chr10:118742908
|
G | A | 2 | a0001c0001t0004g0120a0001c0001t0004g0121 | 2 | HG02523.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.367+11488C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742908 | ||||||
| chr10:118742909
|
G | A | 1 | a0001c0001t0019g0263 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.367+11487C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118742909 | ||||||
| chr10:118743194
|
G | GA | 8 | a0001c0001t0003g0183a0001c0001t0003g0184a0001c0001t0003g0186others(5): Show | 8 | HG02083.hp2 NA18955.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.367+11201dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743194 | ||||||
| chr10:118743248
|
A | G | 12 | a0001c0002t0012g0037a0001c0002t0012g0057a0001c0002t0012g0059others(9): Show | 13 | HG01081.hp1 HG01516.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.367+11148T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743248 | ||||||
| chr10:118743250
|
C | G | 1 | a0001c0001t0051g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.367+11146G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743250 | ||||||
| chr10:118743442
|
T | C | 1 | a0001c0001t0055g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.367+10954A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743442 | ||||||
| chr10:118743557
|
T | G | 1 | a0001c0001t0059g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.367+10839A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743557 | ||||||
| chr10:118743589
|
C | T | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.367+10807G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743589 | ||||||
| chr10:118743598
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+10798C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743598 | ||||||
| chr10:118743653
|
C | T | 8 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(5): Show | 10 | HG02451.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+10743G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743653 | ||||||
| chr10:118743686
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.367+10710C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743686 | ||||||
| chr10:118743691
|
T | C | 1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.367+10705A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743691 | ||||||
| chr10:118743973
|
TTCCA | T | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+10419_367+1042 others(8): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118743973 | ||||||
| chr10:118744045
|
C | A | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+10351G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744045 | ||||||
| chr10:118744123
|
C | T | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.367+10273G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744123 | ||||||
| chr10:118744162
|
G | C | 1 | a0001c0001t0009g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.367+10234C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744162 | ||||||
| chr10:118744197
|
C | T | 1 | a0001c0001t0089g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.367+10199G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744197 | ||||||
| chr10:118744274
|
C | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.367+10122G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744274 | ||||||
| chr10:118744304
|
T | C | 1 | a0001c0001t0055g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.367+10092A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744304 | ||||||
| chr10:118744318
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.367+10078C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744318 | ||||||
| chr10:118744407
|
C | CA | 85 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(82): Show | 93 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.367+9988dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744407 | ||||||
| chr10:118744423
|
C | G | 2 | a0001c0001t0026g0217a0001c0001t0026g0218 | 2 | HG04228.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.367+9973G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744423 | ||||||
| chr10:118744697
|
C | A | 1 | a0001c0001t0086g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.367+9699G>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744697 | ||||||
| chr10:118744719
|
G | A | 1 | a0001c0002t0020g0063 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.367+9677C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744719 | ||||||
| chr10:118744984
|
A | G | 1 | a0001c0001t0092g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.367+9412T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118744984 | ||||||
| chr10:118745069
|
A | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.367+9327T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745069 | ||||||
| chr10:118745278
|
T | C | 88 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(85): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.367+9118A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745278 | ||||||
| chr10:118745324
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.367+9072C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745324 | ||||||
| chr10:118745379
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.367+9017G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745379 | ||||||
| chr10:118745476
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.367+8920C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745476 | ||||||
| chr10:118745547
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(241): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.367+8849A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745547 | ||||||
| chr10:118745560
|
C | CA | 11 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(8): Show | 11 | HG00735.hp1 HG01192.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.367+8835dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745560 | ||||||
| chr10:118745607
|
A | G | 61 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(58): Show | 71 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.367+8789T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745607 | ||||||
| chr10:118745676
|
A | G | 1 | a0001c0001t0007g0301 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+8720T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745676 | ||||||
| chr10:118745857
|
G | C | 1 | a0001c0001t0084g0343 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.367+8539C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745857 | ||||||
| chr10:118745942
|
T | G | 46 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(43): Show | 51 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.367+8454A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745942 | ||||||
| chr10:118745974
|
T | TA | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.367+8421dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745974 | ||||||
| chr10:118745988
|
C | CA | 31 | a0001c0001t0001g0266a0001c0001t0001g0287a0001c0001t0006g0123others(28): Show | 32 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.367+8407dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118745988 | ||||||
| chr10:118746012
|
C | T | 1 | a0001c0001t0010g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.367+8384G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746012 | ||||||
| chr10:118746013
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(98): Show | 110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.367+8383C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746013 | ||||||
| chr10:118746084
|
A | G | 89 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(86): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.367+8312T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746084 | ||||||
| chr10:118746107
|
G | A | 1 | a0001c0001t0100g0191 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.367+8289C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746107 | ||||||
| chr10:118746138
|
C | T | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367+8258G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746138 | ||||||
| chr10:118746151
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0012g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.367+8235_367+8244d others(12): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746151
|
C | CAAAAAAA others(4): Show |
24 | a0001c0001t0003g0159a0001c0001t0010g0136a0001c0001t0010g0151others(21): Show | 25 | HG01074.hp1 HG01081.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.367+8234_367+8244d others(13): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746151
|
C | CAAAAAAA others(5): Show |
38 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0161others(35): Show | 46 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.367+8233_367+8244d others(14): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746151
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0196others(4): Show | 7 | HG00423.hp2 HG01361.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+8232_367+8244d others(15): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746151
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0099g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.367+8231_367+8244d others(16): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746151
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0018g0148 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.367+8244_367+8245i others(21): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746151
|
CAA | C | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.367+8243_367+8244d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746151 | ||||||
| chr10:118746168
|
G | T | 4 | a0001c0001t0004g0012a0001c0001t0004g0070a0001c0001t0056g0068others(1): Show | 5 | HG00323.hp1 HG03239.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+8228C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746168 | ||||||
| chr10:118746896
|
A | C | 1 | a0001c0001t0055g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.367+7500T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118746896 | ||||||
| chr10:118747021
|
G | T | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.367+7375C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747021 | ||||||
| chr10:118747172
|
C | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.367+7224G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747172 | ||||||
| chr10:118747198
|
T | C | 1 | a0001c0001t0006g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.367+7198A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747198 | ||||||
| chr10:118747536
|
C | CA | 47 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0215others(44): Show | 50 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.367+6859dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747536 | ||||||
| chr10:118747536
|
C | CAA | 89 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(86): Show | 97 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.367+6858_367+6859d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747536 | ||||||
| chr10:118747536
|
C | CAAA | 7 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(4): Show | 7 | HG00423.hp1 HG01106.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+6857_367+6859d others(5): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747536 | ||||||
| chr10:118747570
|
CA | C | 89 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(86): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.367+6825delT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747570 | ||||||
| chr10:118747590
|
A | C | 1 | a0001c0001t0102g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.367+6806T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747590 | ||||||
| chr10:118747629
|
C | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.367+6767G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747629 | ||||||
| chr10:118747642
|
G | T | 1 | a0001c0001t0038g0211 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.367+6754C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747642 | ||||||
| chr10:118747697
|
G | T | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367+6699C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747697 | ||||||
| chr10:118747926
|
A | G | 1 | a0001c0001t0016g0011 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.367+6470T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118747926 | ||||||
| chr10:118748032
|
C | T | 3 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0101g0341 | 3 | HG01243.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.367+6364G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748032 | ||||||
| chr10:118748064
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367+6332C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748064 | ||||||
| chr10:118748121
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.367+6275A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748121 | ||||||
| chr10:118748227
|
A | G | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367+6169T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748227 | ||||||
| chr10:118748298
|
G | T | 89 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(86): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.367+6098C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748298 | ||||||
| chr10:118748407
|
T | C | 87 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(84): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.367+5989A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748407 | ||||||
| chr10:118748775
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.367+5621G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748775 | ||||||
| chr10:118748785
|
C | T | 44 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(41): Show | 47 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.367+5611G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748785 | ||||||
| chr10:118748828
|
G | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.367+5568C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748828 | ||||||
| chr10:118748920
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.367+5476C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748920 | ||||||
| chr10:118748973
|
G | A | 1 | a0001c0001t0031g0053 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.367+5423C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748973 | ||||||
| chr10:118748999
|
C | T | 1 | a0001c0001t0071g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.367+5397G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118748999 | ||||||
| chr10:118749046
|
C | T | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367+5350G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749046 | ||||||
| chr10:118749180
|
G | A | 24 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(21): Show | 25 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.367+5216C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749180 | ||||||
| chr10:118749223
|
G | GA | 41 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(38): Show | 44 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.367+5172dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749223 | ||||||
| chr10:118749226
|
T | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(99): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.367+5170A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749226 | ||||||
| chr10:118749302
|
G | C | 1 | a0001c0002t0034g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.367+5094C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749302 | ||||||
| chr10:118749322
|
ATGGCTTG others(9): Show |
A | 1 | a0001c0002t0064g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.367+5058_367+5073d others(18): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749322 | ||||||
| chr10:118749342
|
C | T | 17 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0044others(14): Show | 19 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.367+5054G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749342 | ||||||
| chr10:118749578
|
T | G | 10 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(7): Show | 10 | HG00735.hp1 HG01192.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.367+4818A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749578 | ||||||
| chr10:118749592
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.367+4804C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749592 | ||||||
| chr10:118749614
|
T | G | 26 | a0001c0001t0010g0136a0001c0001t0010g0151a0001c0001t0010g0152others(23): Show | 27 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.367+4782A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749614 | ||||||
| chr10:118749646
|
A | G | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.367+4750T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749646 | ||||||
| chr10:118749805
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.367+4591C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749805 | ||||||
| chr10:118749857
|
CTG | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(41): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.367+4537_367+4538d others(4): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749857 | ||||||
| chr10:118749912
|
G | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(153): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.367+4484C>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749912 | ||||||
| chr10:118749918
|
C | T | 1 | a0001c0001t0002g0340 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.367+4478G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749918 | ||||||
| chr10:118749943
|
C | T | 2 | a0001c0003t0041g0209a0001c0003t0041g0210 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.367+4453G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749943 | ||||||
| chr10:118749965
|
T | C | 1 | a0001c0001t0015g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.367+4431A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749965 | ||||||
| chr10:118749967
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.367+4429C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118749967 | ||||||
| chr10:118750000
|
T | C | 5 | a0001c0001t0001g0208a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG02523.hp2 NA18959.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+4396A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750000 | ||||||
| chr10:118750010
|
T | C | 1 | a0001c0001t0048g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367+4386A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750010 | ||||||
| chr10:118750058
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.367+4338C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750058 | ||||||
| chr10:118750258
|
G | A | 2 | a0001c0001t0004g0128a0001c0001t0004g0129 | 2 | HG01361.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.367+4138C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750258 | ||||||
| chr10:118750322
|
C | CA | 24 | a0001c0001t0001g0026a0001c0001t0001g0207a0001c0001t0001g0280others(21): Show | 26 | HG01081.hp1 HG01099.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.367+4073dupT | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750322 | ||||||
| chr10:118750386
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.367+4010G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750386 | ||||||
| chr10:118750491
|
A | G | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+3905T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750491 | ||||||
| chr10:118750525
|
T | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(99): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.367+3871A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750525 | ||||||
| chr10:118750733
|
G | A | 71 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(68): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.367+3663C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750733 | ||||||
| chr10:118750788
|
A | G | 1 | a0001c0001t0080g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367+3608T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750788 | ||||||
| chr10:118750804
|
A | AC | 245 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(242): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.367+3591_367+3592i others(3): Show |
CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750804 | ||||||
| chr10:118750932
|
G | C | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+3464C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118750932 | ||||||
| chr10:118751211
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.367+3185A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751211 | ||||||
| chr10:118751356
|
T | G | 1 | a0001c0002t0020g0063 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.367+3040A>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751356 | ||||||
| chr10:118751371
|
C | T | 70 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(67): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.367+3025G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751371 | ||||||
| chr10:118751399
|
T | A | 1 | a0001c0001t0024g0289 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.367+2997A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751399 | ||||||
| chr10:118751403
|
C | T | 3 | a0001c0001t0091g0041a0001c0001t0092g0039a0001c0001t0098g0040 | 3 | HG02280.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.367+2993G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751403 | ||||||
| chr10:118751601
|
G | A | 1 | a0001c0001t0052g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.367+2795C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751601 | ||||||
| chr10:118751691
|
A | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(253): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.367+2705T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751691 | ||||||
| chr10:118751691
|
A | T | 1 | a0001c0001t0010g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.367+2705T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751691 | ||||||
| chr10:118751903
|
G | A | 1 | a0001c0001t0104g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.367+2493C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751903 | ||||||
| chr10:118751944
|
A | G | 88 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0159others(85): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.367+2452T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118751944 | ||||||
| chr10:118752164
|
C | T | 1 | a0001c0001t0022g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.367+2232G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752164 | ||||||
| chr10:118752224
|
T | A | 1 | a0001c0001t0004g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.367+2172A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752224 | ||||||
| chr10:118752247
|
A | C | 2 | a0001c0001t0003g0019a0001c0001t0087g0135 | 3 | HG02027.hp2 NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.367+2149T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752247 | ||||||
| chr10:118752252
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0290a0001c0001t0001g0291others(3): Show | 9 | NA18963.hp1 NA18968.hp1 NA18985.hp2 others(6): Show |
intron_variant | MODIFIER | c.367+2144A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752252 | ||||||
| chr10:118752275
|
A | G | 2 | a0001c0002t0012g0037a0001c0002t0035g0008 | 3 | HG02647.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.367+2121T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752275 | ||||||
| chr10:118752277
|
G | A | 2 | a0001c0001t0006g0133a0001c0001t0006g0134 | 2 | NA18941.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.367+2119C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752277 | ||||||
| chr10:118752575
|
A | C | 1 | a0001c0001t0095g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.367+1821T>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752575 | ||||||
| chr10:118752620
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.367+1776T>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752620 | ||||||
| chr10:118752635
|
C | T | 2 | a0001c0001t0079g0206a0001c0001t0080g0205 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367+1761G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752635 | ||||||
| chr10:118752727
|
G | A | 1 | a0001c0001t0081g0295 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.367+1669C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752727 | ||||||
| chr10:118752876
|
C | G | 1 | a0001c0001t0072g0035 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.367+1520G>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752876 | ||||||
| chr10:118752892
|
T | A | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0300others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+1504A>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752892 | ||||||
| chr10:118752977
|
G | A | 46 | a0001c0001t0001g0316a0001c0001t0001g0327a0001c0001t0001g0328others(43): Show | 51 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.367+1419C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118752977 | ||||||
| chr10:118753146
|
G | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(225): Show | 251 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.367+1250C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753146 | ||||||
| chr10:118753239
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.367+1157G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753239 | ||||||
| chr10:118753327
|
C | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(153): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.367+1069G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753327 | ||||||
| chr10:118753345
|
G | A | 1 | a0001c0001t0002g0340 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.367+1051C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753345 | ||||||
| chr10:118753508
|
A | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(154): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.367+888T>C | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753508 | ||||||
| chr10:118753604
|
G | A | 1 | a0001c0001t0016g0202 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367+792C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753604 | ||||||
| chr10:118753911
|
T | C | 2 | a0001c0001t0083g0342a0001c0001t0084g0343 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.367+485A>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753911 | ||||||
| chr10:118753974
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.367+422G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118753974 | ||||||
| chr10:118754196
|
G | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(152): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.367+200C>G | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118754196 | ||||||
| chr10:118754244
|
G | A | 1 | a0001c0001t0001g0344 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.367+152C>T | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118754244 | ||||||
| chr10:118754324
|
C | T | 1 | a0001c0001t0077g0031 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.367+72G>A | CACUL1 | ENSG00000151893.15 | transcript | ENST00000369151.8 | protein_coding | 1/8 | chr10 | 118754324 |