Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51185 |
|---|---|
| ensemblid | ENSG00000113851.16 |
| hgncid | 30185 |
| symbol | CRBN |
| name | cereblon |
| refseq_nuc | NM_016302.4 |
| refseq_prot | NP_057386.2 |
| ensembl_nuc | ENST00000231948.9 |
| ensembl_prot | ENSP00000231948.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 3150011 |
| end | 3179691 |
| strand | - |
| ver | v1.2 |
| region | chr3:3150011-3179691 |
| region5000 | chr3:3145011-3184691 |
| regionname0 | CRBN_chr3_3150011_3179691 |
| regionname5000 | CRBN_chr3_3145011_3184691 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1329 | 231 | 84 | 55 | 50 | 10 | 30 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| c0002 | 0/0 | 1329 | 127 | 0 | 11 | 100 | 2 | 14 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| c0003 | 0/0 | 1329 | 9 | 1 | 0 | 8 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| c0004 | 0/0 | 1329 | 8 | 6 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| c0005 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 858 | 135 | 8 | 13 | 96 | 2 | 16 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0002 | 0/1 | 863 | 107 | 32 | 29 | 27 | 5 | 13 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0003 | 0/0 | 859 | 45 | 11 | 14 | 11 | 2 | 7 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0004 | 1/0 | 859 | 28 | 26 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0005 | 0/0 | 863 | 19 | 5 | 2 | 9 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0006 | 0/0 | 860 | 10 | 1 | 6 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0007 | 0/0 | 858 | 8 | 0 | 0 | 8 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0008 | 0/0 | 854 | 7 | 0 | 1 | 6 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0009 | 0/0 | 858 | 4 | 2 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0010 | 0/0 | 858 | 4 | 3 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0011 | 0/0 | 863 | 2 | 0 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0012 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0013 | 0/0 | 858 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0014 | 0/0 | 872 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0015 | 0/0 | 859 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| t0016 | 0/0 | 858 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 27 | 0 | 1 | 20 | 1 | 5 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0002 | 0/1 | 24 | 1 | 7 | 12 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0003 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0004 | 0/0 | 10 | 1 | 6 | 3 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0005 | 0/0 | 9 | 3 | 2 | 1 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0006 | 0/0 | 9 | 1 | 5 | 2 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0007 | 0/0 | 8 | 0 | 5 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0009 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0012 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0014 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0018 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0019 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0020 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0023 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0027 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1329 | 231 | 84 | 55 | 50 | 10 | 30 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0002 | 0/0 | 1329 | 127 | 0 | 11 | 100 | 2 | 14 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0003 | 0/0 | 1329 | 9 | 1 | 0 | 8 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0004 | 0/0 | 1329 | 8 | 6 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0002c0005 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2186 | 19 | 8 | 4 | 4 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0002 | 0/1 | 2191 | 101 | 28 | 28 | 26 | 5 | 13 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0003 | 0/0 | 2187 | 42 | 9 | 14 | 11 | 2 | 6 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0004 | 1/0 | 2187 | 28 | 26 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0005 | 0/0 | 2191 | 19 | 5 | 2 | 9 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0006 | 0/0 | 2188 | 10 | 1 | 6 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0010 | 0/0 | 2186 | 4 | 3 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0011 | 0/0 | 2191 | 2 | 0 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0012 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0013 | 0/0 | 2186 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0014 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0001t0015 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0002t0001 | 0/0 | 2186 | 116 | 0 | 9 | 92 | 2 | 13 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0002t0002 | 0/0 | 2191 | 2 | 0 | 1 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0002t0003 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0002t0008 | 0/0 | 2182 | 7 | 0 | 1 | 6 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0002t0016 | 0/0 | 2186 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0003t0003 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0003t0007 | 0/0 | 2186 | 8 | 0 | 0 | 8 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0004t0002 | 0/0 | 2191 | 4 | 4 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0001c0004t0009 | 0/0 | 2186 | 4 | 2 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| a0002c0005t0003 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | copy fasta | chr3 | 3145011 | 3184691 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0002 | 0/1 | 24 | 1 | 7 | 12 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0005 | 0/0 | 9 | 3 | 2 | 1 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0006 | 0/0 | 9 | 1 | 5 | 2 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0020 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0004 | 0/0 | 10 | 1 | 6 | 3 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0014 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0023 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0006g0007 | 0/0 | 8 | 0 | 5 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0011g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0012g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0013g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0001 | 0/0 | 27 | 0 | 1 | 20 | 1 | 5 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0003 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0009 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0012 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0019 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0008g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0008g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0008g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0016g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0003t0007g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0003t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0002c0005t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0124 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0151 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00140 | hp1 | a0001 | c0001 | t0015 | g0070 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0067 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0112 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00609 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01106 | hp1 | a0001 | c0004 | t0009 | g0097 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01175 | hp2 | a0001 | c0004 | t0009 | g0110 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0176 | EUR | IBS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0068 | EUR | IBS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0035 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01934 | hp2 | a0001 | c0002 | t0008 | g0056 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02165 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0035 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0094 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02572 | hp2 | a0002 | c0005 | t0003 | g0078 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02602 | hp1 | a0001 | c0001 | t0014 | g0106 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0113 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0099 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02922 | hp2 | a0001 | c0004 | t0009 | g0108 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0060 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0038 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03516 | hp1 | a0001 | c0004 | t0009 | g0109 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0038 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0118 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18940 | hp1 | a0001 | c0003 | t0007 | g0055 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18961 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18965 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18974 | hp1 | a0001 | c0002 | t0008 | g0044 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18977 | hp2 | a0001 | c0002 | t0008 | g0044 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18986 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19005 | hp1 | a0001 | c0002 | t0008 | g0046 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19010 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19012 | hp2 | a0001 | c0002 | t0008 | g0134 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0041 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19054 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19063 | hp1 | a0001 | c0002 | t0008 | g0046 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19074 | hp1 | a0001 | c0002 | t0008 | g0128 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19091 | hp1 | a0001 | c0002 | t0016 | g0131 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | ASW | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0051 | EUR | TSI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0091 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0082 | REF | REF | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3174136
|
C | G | 1 | a0002 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.300G>C | p.Gln100His | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/11 | 304/2187 | 300/1329 | 100/442 | chr3 | 3174136 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3150985
|
C | T | 1 | a0001c0003 | 9 | HG00609.hp2 HG02165.hp1 HG02258.hp2 others(6): Show |
synonymous_variant | LOW | c.1209G>A | p.Thr403Thr | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 1213/2187 | 1209/1329 | 403/442 | chr3 | 3150985 | ||
| chr3:3156234
|
A | G | 1 | a0001c0002 | 127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
synonymous_variant | LOW | c.735T>C | p.Tyr245Tyr | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/11 | 739/2187 | 735/1329 | 245/442 | chr3 | 3156234 | ||
| chr3:3174217
|
G | A | 1 | a0001c0004 | 8 | HG01106.hp1 HG01175.hp2 HG02559.hp1 others(5): Show |
synonymous_variant | LOW | c.219C>T | p.His73His | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/11 | 223/2187 | 219/1329 | 73/442 | chr3 | 3174217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3150030
|
TTTAC | T | 1 | a0001c0002t0008 | 7 | HG01934.hp2 NA18974.hp1 NA18977.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*831_*834delGTAA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 831 | chr3 | 3150030 | |||||
| chr3:3150092
|
T | C | 21 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*773A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 773 | chr3 | 3150092 | |||||
| chr3:3150129
|
T | G | 1 | a0001c0001t0010 | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*736A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 736 | chr3 | 3150129 | |||||
| chr3:3150149
|
A | G | 3 | a0001c0001t0010a0001c0001t0013a0001c0004t0009 | 10 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*716T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 716 | chr3 | 3150149 | |||||
| chr3:3150248
|
A | G | 1 | a0001c0002t0016 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 617 | chr3 | 3150248 | |||||
| chr3:3150272
|
G | C | 1 | a0001c0001t0005 | 19 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*593C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 593 | chr3 | 3150272 | |||||
| chr3:3150322
|
T | TATCTCAG others(25): Show |
1 | a0001c0001t0012 | 2 | HG01891.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*511_*542dupTTCCTT others(26): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 542 | chr3 | 3150322 | |||||
| chr3:3150352
|
G | C | 1 | a0001c0001t0015 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*513C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 513 | chr3 | 3150352 | |||||
| chr3:3150451
|
A | G | 1 | a0001c0001t0011 | 2 | HG03491.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 414 | chr3 | 3150451 | |||||
| chr3:3150459
|
G | A | 1 | a0001c0003t0007 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*406C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 406 | chr3 | 3150459 | |||||
| chr3:3150518
|
A | AT | 1 | a0001c0001t0006 | 10 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*346dupA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 346 | chr3 | 3150518 | |||||
| chr3:3150518
|
AT | A | 9 | a0001c0001t0001a0001c0001t0010a0001c0001t0013others(6): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*346delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 346 | chr3 | 3150518 | |||||
| chr3:3150712
|
T | A | 1 | a0001c0001t0013 | 2 | HG02647.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*153A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 153 | chr3 | 3150712 | |||||
| chr3:3150776
|
A | ACTTAGGT others(7): Show |
1 | a0001c0001t0014 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75_*88dupGATACATA others(6): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 88 | chr3 | 3150776 | |||||
| chr3:3150840
|
A | ATAAC | 5 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(2): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*21_*24dupGTTA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 24 | chr3 | 3150840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3151219
|
C | T | 80 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1149-174G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151219 | ||||||
| chr3:3151243
|
T | G | 53 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(50): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1149-198A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151243 | ||||||
| chr3:3151260
|
G | A | 2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1149-215C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151260 | ||||||
| chr3:3151304
|
A | T | 164 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(161): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1149-259T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151304 | ||||||
| chr3:3151336
|
GACCACAT others(16): Show |
G | 2 | a0001c0001t0001g0101a0001c0002t0001g0117 | 2 | HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1149-314_1149-292d others(25): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151336 | ||||||
| chr3:3151422
|
A | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0166a0001c0001t0002g0167others(1): Show | 4 | HG00642.hp2 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-377T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151422 | ||||||
| chr3:3151449
|
T | A | 1 | a0001c0002t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1149-404A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151449 | ||||||
| chr3:3151492
|
G | A | 164 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(161): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1149-447C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151492 | ||||||
| chr3:3151502
|
A | AAAAACTA others(1): Show |
92 | a0001c0001t0001g0037a0001c0001t0002g0002a0001c0001t0002g0005others(89): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1149-458_1149-457i others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151502 | ||||||
| chr3:3151528
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0158 | 6 | HG02071.hp1 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-483C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151528 | ||||||
| chr3:3151555
|
G | GGTATTTT others(4): Show |
1 | a0001c0001t0002g0155 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1149-521_1149-511d others(13): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151555 | ||||||
| chr3:3151704
|
T | G | 165 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(162): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1149-659A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151704 | ||||||
| chr3:3151781
|
G | GGGAACTG others(1): Show |
3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1148+667_1148+674d others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151781 | ||||||
| chr3:3151827
|
G | GCAAACAA others(1): Show |
137 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(134): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1148+621_1148+628d others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151827 | ||||||
| chr3:3151828
|
C | CAAACAAA others(1): Show |
28 | a0001c0001t0002g0076a0001c0001t0003g0004a0001c0001t0003g0015others(25): Show | 54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1148+627_1148+628i others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151828 | ||||||
| chr3:3151915
|
C | T | 1 | a0001c0002t0008g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1148+541G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151915 | ||||||
| chr3:3151938
|
T | C | 3 | a0001c0001t0005g0023a0001c0001t0005g0051a0001c0001t0005g0169 | 7 | HG01106.hp2 HG01261.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+518A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151938 | ||||||
| chr3:3151962
|
G | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1148+494C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151962 | ||||||
| chr3:3151992
|
A | G | 87 | a0001c0001t0001g0037a0001c0001t0002g0002a0001c0001t0002g0005others(84): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1148+464T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151992 | ||||||
| chr3:3152016
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1148+440A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152016 | ||||||
| chr3:3152104
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1148+352G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152104 | ||||||
| chr3:3152142
|
T | A | 53 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(50): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1148+314A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152142 | ||||||
| chr3:3152150
|
A | ATTT | 74 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1148+303_1148+305d others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152150 | ||||||
| chr3:3152159
|
T | TTTC | 8 | a0001c0001t0001g0037a0001c0001t0002g0063a0001c0001t0002g0166others(5): Show | 10 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1148+296_1148+297i others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152159 | ||||||
| chr3:3152165
|
T | A | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+291A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152165 | ||||||
| chr3:3152166
|
A | AAT | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+289_1148+290i others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152166 | ||||||
| chr3:3152219
|
T | C | 75 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(72): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1148+237A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152219 | ||||||
| chr3:3152264
|
T | A | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148+192A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152264 | ||||||
| chr3:3152273
|
A | C | 165 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(162): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1148+183T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152273 | ||||||
| chr3:3152404
|
C | T | 1 | a0001c0001t0006g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1148+52G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152404 | ||||||
| chr3:3152423
|
G | GA | 81 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(78): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1148+32dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152423 | ||||||
| chr3:3152641
|
T | C | 5 | a0001c0002t0008g0044a0001c0002t0008g0046a0001c0002t0008g0056others(2): Show | 7 | HG01934.hp2 NA18974.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1017-54A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152641 | ||||||
| chr3:3152651
|
A | G | 1 | a0001c0002t0001g0132 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1017-64T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152651 | ||||||
| chr3:3152685
|
T | G | 8 | a0001c0001t0001g0037a0001c0001t0002g0063a0001c0001t0002g0166others(5): Show | 10 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1017-98A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152685 | ||||||
| chr3:3152744
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1017-157A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152744 | ||||||
| chr3:3152879
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0013g0041 | 3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1017-292T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152879 | ||||||
| chr3:3152894
|
T | C | 1 | a0001c0002t0001g0009 | 7 | HG00741.hp2 HG01069.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1017-307A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152894 | ||||||
| chr3:3152903
|
G | A | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1017-316C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152903 | ||||||
| chr3:3153210
|
G | A | 1 | a0001c0001t0006g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1016+214C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153210 | ||||||
| chr3:3153229
|
T | A | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1016+195A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153229 | ||||||
| chr3:3153238
|
T | C | 5 | a0001c0001t0002g0158a0001c0002t0001g0013a0001c0002t0001g0132others(2): Show | 10 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1016+186A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153238 | ||||||
| chr3:3153261
|
A | G | 1 | a0001c0001t0004g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1016+163T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153261 | ||||||
| chr3:3153367
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1016+57T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153367 | ||||||
| chr3:3153641
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0002g0063a0001c0001t0002g0166others(5): Show | 10 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.952-153A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153641 | ||||||
| chr3:3153667
|
G | A | 5 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0085others(2): Show | 13 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.952-179C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153667 | ||||||
| chr3:3153685
|
A | G | 26 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0030others(23): Show | 51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.952-197T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153685 | ||||||
| chr3:3153812
|
T | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.951+148A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153812 | ||||||
| chr3:3153819
|
G | T | 1 | a0001c0001t0003g0033 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.951+141C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153819 | ||||||
| chr3:3153870
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.951+90G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153870 | ||||||
| chr3:3153890
|
C | T | 26 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0030others(23): Show | 51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.951+70G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153890 | ||||||
| chr3:3154166
|
C | G | 56 | a0001c0001t0002g0158a0001c0002t0001g0001a0001c0002t0001g0003others(53): Show | 127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.836-91G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154166 | ||||||
| chr3:3154209
|
C | T | 1 | a0001c0001t0002g0027 | 3 | HG02602.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.836-134G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154209 | ||||||
| chr3:3154253
|
A | G | 1 | a0001c0001t0006g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-178T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154253 | ||||||
| chr3:3154288
|
A | G | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.836-213T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154288 | ||||||
| chr3:3154379
|
TAAAG | T | 70 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(67): Show | 150 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.836-308_836-305del others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154379 | ||||||
| chr3:3154518
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.835+229A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154518 | ||||||
| chr3:3154558
|
G | C | 1 | a0001c0001t0002g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.835+189C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154558 | ||||||
| chr3:3154589
|
AT | A | 164 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(161): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.835+157delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154589 | ||||||
| chr3:3154726
|
C | G | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.835+21G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154726 | ||||||
| chr3:3154969
|
A | G | 1 | a0001c0002t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.751-138T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3154969 | ||||||
| chr3:3155152
|
C | T | 164 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(161): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.751-321G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155152 | ||||||
| chr3:3155315
|
G | C | 1 | a0001c0001t0003g0033 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.751-484C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155315 | ||||||
| chr3:3155329
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.751-498A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155329 | ||||||
| chr3:3155351
|
T | G | 97 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(94): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.751-520A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155351 | ||||||
| chr3:3155378
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0003g0111others(1): Show | 6 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.751-547A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155378 | ||||||
| chr3:3155445
|
T | C | 1 | a0001c0001t0002g0050 | 2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.751-614A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155445 | ||||||
| chr3:3155447
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-616C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155447 | ||||||
| chr3:3155461
|
C | A | 1 | a0001c0001t0002g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.751-630G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155461 | ||||||
| chr3:3155675
|
G | A | 1 | a0001c0001t0003g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.750+544C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155675 | ||||||
| chr3:3155677
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.750+542G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155677 | ||||||
| chr3:3155810
|
C | CT | 98 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(95): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.750+408dupA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155810 | ||||||
| chr3:3155820
|
C | T | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.750+399G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155820 | ||||||
| chr3:3155956
|
G | A | 1 | a0001c0001t0003g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.750+263C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155956 | ||||||
| chr3:3156064
|
A | C | 10 | a0001c0001t0003g0111a0001c0001t0010g0060a0001c0001t0010g0099others(7): Show | 11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.750+155T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156064 | ||||||
| chr3:3156116
|
A | G | 1 | a0001c0001t0010g0112 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.750+103T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156116 | ||||||
| chr3:3156132
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.750+87A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156132 | ||||||
| chr3:3156187
|
T | C | 165 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(162): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.750+32A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156187 | ||||||
| chr3:3156426
|
G | T | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-145C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156426 | ||||||
| chr3:3156474
|
T | C | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688-193A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156474 | ||||||
| chr3:3156537
|
A | G | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-256T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156537 | ||||||
| chr3:3156696
|
G | T | 93 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(90): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.688-415C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156696 | ||||||
| chr3:3156829
|
C | T | 65 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(62): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.688-548G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156829 | ||||||
| chr3:3157125
|
A | G | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-844T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157125 | ||||||
| chr3:3157164
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.688-883A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157164 | ||||||
| chr3:3157262
|
A | G | 9 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0026others(6): Show | 22 | HG00438.hp2 HG02015.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.688-981T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157262 | ||||||
| chr3:3157486
|
T | G | 67 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(64): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.688-1205A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157486 | ||||||
| chr3:3157555
|
G | C | 1 | a0001c0004t0009g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.688-1274C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157555 | ||||||
| chr3:3157586
|
C | G | 1 | a0001c0004t0009g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.688-1305G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157586 | ||||||
| chr3:3157594
|
A | T | 173 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(170): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.688-1313T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157594 | ||||||
| chr3:3157610
|
C | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0073a0001c0001t0003g0077 | 12 | HG00597.hp2 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.688-1329G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157610 | ||||||
| chr3:3157780
|
T | G | 1 | a0001c0002t0001g0026 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.688-1499A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157780 | ||||||
| chr3:3157813
|
G | C | 2 | a0001c0004t0009g0097a0001c0004t0009g0110 | 2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.688-1532C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157813 | ||||||
| chr3:3157834
|
A | C | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.688-1553T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157834 | ||||||
| chr3:3157890
|
T | C | 1 | a0001c0002t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.688-1609A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157890 | ||||||
| chr3:3157951
|
A | C | 121 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(118): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.688-1670T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157951 | ||||||
| chr3:3158035
|
A | G | 70 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(67): Show | 151 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.688-1754T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158035 | ||||||
| chr3:3158107
|
G | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(87): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.688-1826C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158107 | ||||||
| chr3:3158116
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.688-1835T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158116 | ||||||
| chr3:3158231
|
A | G | 1 | a0001c0002t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.688-1950T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158231 | ||||||
| chr3:3158329
|
C | T | 26 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0030others(23): Show | 52 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.688-2048G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158329 | ||||||
| chr3:3158357
|
A | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-2076T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158357 | ||||||
| chr3:3158406
|
G | C | 3 | a0001c0001t0002g0063a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG00642.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.688-2125C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158406 | ||||||
| chr3:3158433
|
T | C | 1 | a0001c0002t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.688-2152A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158433 | ||||||
| chr3:3158532
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-2251A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158532 | ||||||
| chr3:3158844
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.688-2563C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158844 | ||||||
| chr3:3159007
|
G | T | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.688-2726C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159007 | ||||||
| chr3:3159008
|
A | C | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(160): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.688-2727T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159008 | ||||||
| chr3:3159095
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688-2814G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159095 | ||||||
| chr3:3159164
|
C | T | 3 | a0001c0001t0005g0169a0001c0004t0002g0025a0001c0004t0002g0091 | 5 | HG01106.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-2883G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159164 | ||||||
| chr3:3159165
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.688-2884C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159165 | ||||||
| chr3:3159191
|
T | C | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688-2910A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159191 | ||||||
| chr3:3159279
|
C | G | 165 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(162): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.688-2998G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159279 | ||||||
| chr3:3159536
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-3255C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159536 | ||||||
| chr3:3159621
|
A | G | 1 | a0001c0001t0003g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.688-3340T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159621 | ||||||
| chr3:3159748
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(38): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.688-3467A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159748 | ||||||
| chr3:3159852
|
A | C | 1 | a0001c0001t0002g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.688-3571T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159852 | ||||||
| chr3:3159957
|
G | T | 47 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0020others(44): Show | 103 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.688-3676C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159957 | ||||||
| chr3:3160058
|
G | T | 1 | a0001c0001t0005g0169 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.688-3777C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160058 | ||||||
| chr3:3160096
|
G | C | 52 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0002g0170others(49): Show | 95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.688-3815C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160096 | ||||||
| chr3:3160595
|
T | C | 28 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0003g0004others(25): Show | 54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.688-4314A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160595 | ||||||
| chr3:3160608
|
A | G | 47 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0027others(44): Show | 98 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.688-4327T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160608 | ||||||
| chr3:3160631
|
T | C | 1 | a0001c0002t0001g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.688-4350A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160631 | ||||||
| chr3:3160662
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.688-4381T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160662 | ||||||
| chr3:3160669
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.688-4388A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160669 | ||||||
| chr3:3160961
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.688-4680T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160961 | ||||||
| chr3:3160998
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0125 | 2 | NA18944.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.688-4717G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160998 | ||||||
| chr3:3161081
|
T | G | 2 | a0001c0004t0009g0097a0001c0004t0009g0110 | 2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.688-4800A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161081 | ||||||
| chr3:3161151
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.688-4870G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161151 | ||||||
| chr3:3161430
|
CAAT | C | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-5152_688-5150d others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161430 | ||||||
| chr3:3161462
|
T | C | 1 | a0001c0004t0009g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.688-5181A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161462 | ||||||
| chr3:3161474
|
C | T | 6 | a0001c0001t0003g0111a0001c0001t0013g0041a0001c0004t0009g0097others(3): Show | 7 | HG01106.hp1 HG01175.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.688-5193G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161474 | ||||||
| chr3:3161656
|
G | T | 1 | a0001c0002t0001g0026 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.688-5375C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161656 | ||||||
| chr3:3161693
|
T | C | 1 | a0001c0001t0004g0036 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.688-5412A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161693 | ||||||
| chr3:3161735
|
G | A | 177 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(174): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.688-5454C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161735 | ||||||
| chr3:3161773
|
T | G | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-5492A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161773 | ||||||
| chr3:3161789
|
G | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-5508C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161789 | ||||||
| chr3:3161820
|
A | G | 69 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(66): Show | 150 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.688-5539T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161820 | ||||||
| chr3:3161922
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.688-5641T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161922 | ||||||
| chr3:3162079
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.687+5555C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162079 | ||||||
| chr3:3162086
|
G | A | 1 | a0001c0004t0009g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.687+5548C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162086 | ||||||
| chr3:3162123
|
G | A | 2 | a0001c0001t0004g0083a0001c0001t0004g0084 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.687+5511C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162123 | ||||||
| chr3:3162154
|
G | T | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+5480C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162154 | ||||||
| chr3:3162196
|
A | G | 1 | a0001c0001t0011g0038 | 2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.687+5438T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162196 | ||||||
| chr3:3162200
|
T | C | 1 | a0001c0001t0003g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.687+5434A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162200 | ||||||
| chr3:3162242
|
A | G | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+5392T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162242 | ||||||
| chr3:3162316
|
C | T | 26 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0030others(23): Show | 52 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.687+5318G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162316 | ||||||
| chr3:3162347
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+5287C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162347 | ||||||
| chr3:3162353
|
C | G | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+5281G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162353 | ||||||
| chr3:3162405
|
G | A | 165 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(162): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.687+5229C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162405 | ||||||
| chr3:3162408
|
G | A | 1 | a0001c0002t0001g0104 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.687+5226C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162408 | ||||||
| chr3:3162614
|
T | A | 165 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(162): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.687+5020A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162614 | ||||||
| chr3:3162645
|
C | T | 2 | a0001c0002t0001g0124a0001c0002t0002g0123 | 2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.687+4989G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162645 | ||||||
| chr3:3162660
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+4974A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162660 | ||||||
| chr3:3162694
|
ACTTTAAG others(2): Show |
A | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+4931_687+4939d others(11): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162694 | ||||||
| chr3:3162709
|
T | G | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+4925A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162709 | ||||||
| chr3:3162755
|
G | C | 1 | a0001c0002t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.687+4879C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162755 | ||||||
| chr3:3162791
|
T | C | 8 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0026others(5): Show | 21 | HG00438.hp2 HG02015.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.687+4843A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162791 | ||||||
| chr3:3162928
|
C | A | 1 | a0001c0001t0002g0048 | 2 | HG00323.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.687+4706G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162928 | ||||||
| chr3:3163016
|
T | C | 149 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(146): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.687+4618A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163016 | ||||||
| chr3:3163049
|
G | A | 167 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(164): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.687+4585C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163049 | ||||||
| chr3:3163071
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.687+4563C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163071 | ||||||
| chr3:3163120
|
T | C | 148 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(145): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.687+4514A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163120 | ||||||
| chr3:3163122
|
G | C | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+4512C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163122 | ||||||
| chr3:3163205
|
T | C | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(160): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.687+4429A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163205 | ||||||
| chr3:3163238
|
C | T | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+4396G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163238 | ||||||
| chr3:3163258
|
T | G | 1 | a0001c0001t0014g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.687+4376A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163258 | ||||||
| chr3:3163274
|
C | G | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+4360G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163274 | ||||||
| chr3:3163385
|
C | T | 8 | a0001c0002t0001g0019a0001c0002t0001g0043a0001c0002t0001g0045others(5): Show | 15 | HG00408.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.687+4249G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163385 | ||||||
| chr3:3163455
|
C | CA | 65 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(62): Show | 144 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.687+4178dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163455 | ||||||
| chr3:3163458
|
T | G | 65 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(62): Show | 144 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.687+4176A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163458 | ||||||
| chr3:3163662
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.687+3972G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163662 | ||||||
| chr3:3163748
|
G | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(42): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.687+3886C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163748 | ||||||
| chr3:3163771
|
A | T | 1 | a0001c0001t0005g0052 | 2 | NA18956.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.687+3863T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163771 | ||||||
| chr3:3163831
|
A | C | 36 | a0001c0001t0002g0076a0001c0001t0002g0170a0001c0001t0003g0004others(33): Show | 71 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.687+3803T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163831 | ||||||
| chr3:3163832
|
A | C | 1 | a0001c0001t0003g0074 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.687+3802T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163832 | ||||||
| chr3:3163840
|
A | G | 161 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(158): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.687+3794T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163840 | ||||||
| chr3:3163849
|
T | C | 13 | a0001c0001t0003g0111a0001c0001t0010g0060a0001c0001t0010g0099others(10): Show | 20 | HG00280.hp2 HG00609.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.687+3785A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163849 | ||||||
| chr3:3163867
|
C | G | 1 | a0001c0001t0006g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.687+3767G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163867 | ||||||
| chr3:3164155
|
C | T | 1 | a0001c0001t0002g0049 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.687+3479G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164155 | ||||||
| chr3:3164235
|
C | A | 2 | a0001c0001t0003g0111a0001c0001t0013g0041 | 3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.687+3399G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164235 | ||||||
| chr3:3164401
|
C | A | 1 | a0001c0001t0002g0028 | 3 | HG03098.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.687+3233G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164401 | ||||||
| chr3:3164409
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0153 | 2 | HG01074.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.687+3225G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164409 | ||||||
| chr3:3164464
|
G | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+3170C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164464 | ||||||
| chr3:3164478
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.687+3156C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164478 | ||||||
| chr3:3164511
|
G | C | 2 | a0001c0001t0003g0111a0001c0001t0013g0041 | 3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.687+3123C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164511 | ||||||
| chr3:3164552
|
G | C | 1 | a0001c0002t0001g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.687+3082C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164552 | ||||||
| chr3:3164597
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(37): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.687+3037G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164597 | ||||||
| chr3:3164829
|
C | T | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+2805G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164829 | ||||||
| chr3:3164872
|
C | G | 1 | a0001c0001t0002g0048 | 2 | HG00323.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.687+2762G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164872 | ||||||
| chr3:3164929
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.687+2705C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164929 | ||||||
| chr3:3164968
|
C | T | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+2666G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164968 | ||||||
| chr3:3165022
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687+2612G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165022 | ||||||
| chr3:3165075
|
C | A | 1 | a0001c0002t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.687+2559G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165075 | ||||||
| chr3:3165086
|
G | A | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+2548C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165086 | ||||||
| chr3:3165149
|
C | T | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+2485G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165149 | ||||||
| chr3:3165198
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0012g0035 | 4 | HG01891.hp2 HG02257.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+2436C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165198 | ||||||
| chr3:3165327
|
G | C | 1 | a0001c0001t0003g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.687+2307C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165327 | ||||||
| chr3:3165363
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.687+2271C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165363 | ||||||
| chr3:3165366
|
G | A | 1 | a0001c0002t0008g0134 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.687+2268C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165366 | ||||||
| chr3:3165422
|
G | A | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(160): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.687+2212C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165422 | ||||||
| chr3:3165423
|
T | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+2211A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165423 | ||||||
| chr3:3165670
|
T | C | 1 | a0001c0002t0001g0116 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.687+1964A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165670 | ||||||
| chr3:3165674
|
G | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1960C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165674 | ||||||
| chr3:3165759
|
C | T | 1 | a0001c0003t0007g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.687+1875G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165759 | ||||||
| chr3:3165775
|
C | A | 1 | a0001c0001t0003g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.687+1859G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165775 | ||||||
| chr3:3165791
|
T | C | 4 | a0001c0001t0010g0060a0001c0001t0010g0099a0001c0001t0010g0112others(1): Show | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1843A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165791 | ||||||
| chr3:3165830
|
C | G | 1 | a0001c0001t0003g0074 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.687+1804G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165830 | ||||||
| chr3:3165977
|
A | C | 2 | a0001c0001t0004g0029a0001c0001t0004g0059 | 3 | HG02109.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1657T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165977 | ||||||
| chr3:3166037
|
G | C | 4 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0071others(1): Show | 6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1597C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166037 | ||||||
| chr3:3166037
|
G | T | 1 | a0001c0001t0006g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.687+1597C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166037 | ||||||
| chr3:3166054
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.687+1580C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166054 | ||||||
| chr3:3166070
|
T | C | 147 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(144): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.687+1564A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166070 | ||||||
| chr3:3166081
|
G | C | 4 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0071others(1): Show | 6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1553C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166081 | ||||||
| chr3:3166098
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.687+1536G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166098 | ||||||
| chr3:3166164
|
CAT | C | 71 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(68): Show | 160 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.687+1468_687+1469d others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166164 | ||||||
| chr3:3166325
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.687+1309C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166325 | ||||||
| chr3:3166467
|
C | T | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+1167G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166467 | ||||||
| chr3:3166487
|
C | A | 2 | a0001c0001t0004g0029a0001c0001t0004g0059 | 3 | HG02109.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1147G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166487 | ||||||
| chr3:3166558
|
G | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1076C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166558 | ||||||
| chr3:3166730
|
A | G | 175 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(172): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.687+904T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166730 | ||||||
| chr3:3166765
|
A | C | 1 | a0001c0001t0002g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.687+869T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166765 | ||||||
| chr3:3166790
|
A | G | 5 | a0001c0001t0002g0005a0001c0001t0002g0146a0001c0001t0002g0153others(2): Show | 13 | HG01074.hp2 HG01109.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.687+844T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166790 | ||||||
| chr3:3166914
|
G | C | 3 | a0001c0003t0003g0094a0001c0004t0002g0025a0001c0004t0002g0091 | 5 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+720C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166914 | ||||||
| chr3:3166935
|
TA | T | 62 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0100others(59): Show | 139 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.687+698delT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166935 | ||||||
| chr3:3166955
|
G | A | 1 | a0001c0002t0001g0135 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.687+679C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166955 | ||||||
| chr3:3167031
|
T | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+603A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167031 | ||||||
| chr3:3167047
|
C | T | 39 | a0001c0001t0002g0076a0001c0001t0002g0170a0001c0001t0003g0004others(36): Show | 75 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.687+587G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167047 | ||||||
| chr3:3167048
|
G | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(58): Show | 139 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.687+586C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167048 | ||||||
| chr3:3167050
|
G | A | 1 | a0001c0002t0001g0045 | 2 | NA18967.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.687+584C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167050 | ||||||
| chr3:3167078
|
T | C | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(160): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.687+556A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167078 | ||||||
| chr3:3167365
|
C | T | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+269G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167365 | ||||||
| chr3:3167373
|
T | A | 5 | a0001c0002t0001g0003a0001c0002t0001g0040a0001c0002t0001g0104others(2): Show | 16 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.687+261A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167373 | ||||||
| chr3:3167388
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.687+246C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167388 | ||||||
| chr3:3167558
|
G | T | 20 | a0001c0001t0003g0004a0001c0001t0003g0030a0001c0001t0003g0031others(17): Show | 41 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.687+76C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167558 | ||||||
| chr3:3167578
|
G | GA | 3 | a0001c0001t0002g0164a0001c0001t0003g0015a0001c0001t0003g0079 | 7 | HG00438.hp1 HG02155.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.687+55dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167578 | ||||||
| chr3:3167834
|
T | C | 3 | a0001c0003t0003g0094a0001c0004t0002g0025a0001c0004t0002g0091 | 5 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-41A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3167834 | ||||||
| chr3:3167971
|
A | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.528-178T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3167971 | ||||||
| chr3:3168109
|
C | A | 10 | a0001c0001t0002g0170a0001c0001t0005g0014a0001c0001t0005g0023others(7): Show | 20 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.528-316G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168109 | ||||||
| chr3:3168153
|
A | G | 1 | a0001c0002t0001g0012 | 6 | HG01261.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-360T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168153 | ||||||
| chr3:3168156
|
C | A | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-363G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168156 | ||||||
| chr3:3168158
|
C | T | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-365G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168158 | ||||||
| chr3:3168159
|
C | T | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-366G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168159 | ||||||
| chr3:3168161
|
A | G | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-368T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168161 | ||||||
| chr3:3168224
|
CATCTA | C | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.528-436_528-432del others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168224 | ||||||
| chr3:3168225
|
A | T | 1 | a0001c0001t0006g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.528-432T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168225 | ||||||
| chr3:3168348
|
T | G | 68 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(65): Show | 147 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.528-555A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168348 | ||||||
| chr3:3168489
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.528-696C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168489 | ||||||
| chr3:3168500
|
G | A | 2 | a0001c0001t0004g0083a0001c0001t0004g0084 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.528-707C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168500 | ||||||
| chr3:3168521
|
T | C | 1 | a0001c0002t0008g0046 | 2 | NA19005.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.528-728A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168521 | ||||||
| chr3:3168625
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.528-832A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168625 | ||||||
| chr3:3168652
|
T | G | 45 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(42): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.528-859A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168652 | ||||||
| chr3:3168892
|
TC | T | 2 | a0001c0004t0002g0025a0001c0004t0002g0091 | 4 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-1100delG | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168892 | ||||||
| chr3:3168921
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.528-1128A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168921 | ||||||
| chr3:3168928
|
A | C | 1 | a0001c0001t0001g0021 | 4 | HG00597.hp1 HG02738.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-1135T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168928 | ||||||
| chr3:3169015
|
T | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.528-1222A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169015 | ||||||
| chr3:3169059
|
T | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-1266A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169059 | ||||||
| chr3:3169093
|
C | G | 1 | a0001c0001t0013g0041 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.528-1300G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169093 | ||||||
| chr3:3169103
|
A | T | 2 | a0001c0002t0001g0043a0001c0002t0001g0119 | 3 | NA18998.hp1 NA19011.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.528-1310T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169103 | ||||||
| chr3:3169140
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.528-1347G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169140 | ||||||
| chr3:3169157
|
T | C | 13 | a0001c0001t0002g0028a0001c0001t0002g0149a0001c0001t0002g0150others(10): Show | 16 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.528-1364A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169157 | ||||||
| chr3:3169189
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.528-1396A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169189 | ||||||
| chr3:3169210
|
T | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.528-1417A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169210 | ||||||
| chr3:3169233
|
A | G | 1 | a0001c0001t0010g0112 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.528-1440T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169233 | ||||||
| chr3:3169368
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.528-1575T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169368 | ||||||
| chr3:3169474
|
A | ATAG | 149 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(146): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.528-1684_528-1682d others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169474 | ||||||
| chr3:3169535
|
T | G | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-1742A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169535 | ||||||
| chr3:3169650
|
T | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-1857A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169650 | ||||||
| chr3:3169685
|
A | C | 10 | a0001c0001t0002g0170a0001c0001t0005g0014a0001c0001t0005g0023others(7): Show | 20 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.528-1892T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169685 | ||||||
| chr3:3169788
|
A | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.528-1995T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169788 | ||||||
| chr3:3169831
|
T | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(39): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.528-2038A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169831 | ||||||
| chr3:3169871
|
C | G | 23 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0020others(20): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.528-2078G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169871 | ||||||
| chr3:3169888
|
G | A | 2 | a0001c0004t0002g0025a0001c0004t0002g0091 | 4 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-2095C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169888 | ||||||
| chr3:3169896
|
T | TA | 148 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(145): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.528-2104dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169896 | ||||||
| chr3:3169936
|
C | G | 45 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(42): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.528-2143G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169936 | ||||||
| chr3:3170102
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528-2309G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170102 | ||||||
| chr3:3170307
|
G | A | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.527+2469C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170307 | ||||||
| chr3:3170322
|
A | C | 2 | a0001c0002t0001g0117a0001c0002t0003g0118 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.527+2454T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170322 | ||||||
| chr3:3170454
|
C | G | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+2322G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170454 | ||||||
| chr3:3170570
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.527+2206A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170570 | ||||||
| chr3:3170582
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.527+2194G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170582 | ||||||
| chr3:3170609
|
T | C | 1 | a0001c0002t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.527+2167A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170609 | ||||||
| chr3:3170745
|
A | G | 10 | a0001c0001t0003g0111a0001c0001t0010g0060a0001c0001t0010g0099others(7): Show | 11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.527+2031T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170745 | ||||||
| chr3:3170816
|
T | C | 1 | a0001c0002t0001g0139 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.527+1960A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170816 | ||||||
| chr3:3170931
|
T | A | 167 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(164): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.527+1845A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170931 | ||||||
| chr3:3170946
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.527+1830G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170946 | ||||||
| chr3:3170962
|
T | C | 148 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(145): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.527+1814A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170962 | ||||||
| chr3:3170976
|
T | C | 148 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(145): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.527+1800A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170976 | ||||||
| chr3:3171052
|
G | A | 1 | a0001c0004t0009g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.527+1724C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171052 | ||||||
| chr3:3171070
|
A | G | 149 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(146): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.527+1706T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171070 | ||||||
| chr3:3171215
|
T | C | 15 | a0001c0001t0003g0111a0001c0001t0004g0087a0001c0001t0010g0060others(12): Show | 24 | HG00280.hp2 HG00609.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.527+1561A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171215 | ||||||
| chr3:3171302
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.527+1474A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171302 | ||||||
| chr3:3171578
|
A | G | 166 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(163): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.527+1198T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171578 | ||||||
| chr3:3171586
|
T | G | 11 | a0001c0001t0002g0170a0001c0001t0003g0062a0001c0001t0005g0014others(8): Show | 21 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.527+1190A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171586 | ||||||
| chr3:3171618
|
A | T | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.527+1158T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171618 | ||||||
| chr3:3171857
|
G | C | 1 | a0001c0001t0004g0017 | 5 | HG02647.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+919C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171857 | ||||||
| chr3:3171997
|
G | A | 167 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(164): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.527+779C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171997 | ||||||
| chr3:3172005
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(36): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.527+771C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172005 | ||||||
| chr3:3172037
|
T | C | 1 | a0001c0002t0001g0140 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.527+739A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172037 | ||||||
| chr3:3172091
|
G | A | 25 | a0001c0001t0002g0076a0001c0001t0003g0004a0001c0001t0003g0015others(22): Show | 50 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.527+685C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172091 | ||||||
| chr3:3172103
|
C | A | 1 | a0001c0002t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.527+673G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172103 | ||||||
| chr3:3172127
|
T | A | 80 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.527+649A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172127 | ||||||
| chr3:3172146
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.527+630A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172146 | ||||||
| chr3:3172653
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.527+123T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172653 | ||||||
| chr3:3172704
|
A | G | 1 | a0001c0002t0001g0042 | 2 | NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.527+72T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172704 | ||||||
| chr3:3172770
|
T | G | 1 | a0001c0002t0001g0142 | 1 | NA18953.hp2 | splice_region_variant&intron_variant | LOW | c.527+6A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172770 | ||||||
| chr3:3173052
|
T | TTTTA | 8 | a0001c0003t0007g0008a0001c0003t0007g0055a0001c0004t0002g0025others(5): Show | 16 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.378-131_378-128dup others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173052 | ||||||
| chr3:3173088
|
C | T | 48 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(45): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.378-163G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173088 | ||||||
| chr3:3173184
|
A | C | 1 | a0001c0001t0003g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.378-259T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173184 | ||||||
| chr3:3173247
|
G | A | 6 | a0001c0004t0002g0025a0001c0004t0002g0091a0001c0004t0009g0097others(3): Show | 8 | HG01106.hp1 HG01175.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-322C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173247 | ||||||
| chr3:3173403
|
T | G | 2 | a0001c0002t0001g0047a0001c0002t0001g0143 | 3 | NA18947.hp2 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.378-478A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173403 | ||||||
| chr3:3173571
|
G | A | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.377+488C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173571 | ||||||
| chr3:3173843
|
T | C | 1 | a0001c0001t0014g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.377+216A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173843 | ||||||
| chr3:3173924
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0100 | 3 | HG02055.hp2 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.377+135G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173924 | ||||||
| chr3:3173955
|
C | G | 1 | a0001c0001t0003g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.377+104G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173955 | ||||||
| chr3:3173993
|
C | A | 1 | a0001c0001t0003g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.377+66G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173993 | ||||||
| chr3:3174032
|
T | G | 1 | a0001c0002t0001g0143 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.377+27A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3174032 | ||||||
| chr3:3174047
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377+12G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3174047 | ||||||
| chr3:3174270
|
A | G | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(160): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.175-9T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174270 | ||||||
| chr3:3174302
|
T | C | 1 | a0001c0002t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.175-41A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174302 | ||||||
| chr3:3174372
|
G | A | 5 | a0001c0001t0003g0111a0001c0001t0010g0099a0001c0001t0010g0112others(2): Show | 6 | HG00280.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-111C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174372 | ||||||
| chr3:3174594
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.175-333A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174594 | ||||||
| chr3:3174635
|
A | C | 4 | a0001c0004t0009g0097a0001c0004t0009g0108a0001c0004t0009g0109others(1): Show | 4 | HG01106.hp1 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-374T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174635 | ||||||
| chr3:3174684
|
TAATA | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.175-427_175-424del others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174684 | ||||||
| chr3:3174732
|
C | T | 1 | a0001c0002t0001g0026 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.174+431G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174732 | ||||||
| chr3:3174791
|
T | C | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+372A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174791 | ||||||
| chr3:3174876
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+287A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174876 | ||||||
| chr3:3174913
|
G | T | 1 | a0002c0005t0003g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.174+250C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174913 | ||||||
| chr3:3174938
|
C | T | 82 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.174+225G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174938 | ||||||
| chr3:3175030
|
T | A | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+133A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175030 | ||||||
| chr3:3175032
|
G | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+131C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175032 | ||||||
| chr3:3175033
|
C | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+130G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175033 | ||||||
| chr3:3175037
|
T | TGAGG | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+125_174+126ins others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175037 | ||||||
| chr3:3175039
|
G | C | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+124C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175039 | ||||||
| chr3:3175040
|
C | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+123G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175040 | ||||||
| chr3:3175041
|
C | A | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.174+122G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175041 | ||||||
| chr3:3175292
|
GA | G | 7 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0013g0041others(4): Show | 16 | HG00609.hp2 HG02165.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-24delT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175292 | ||||||
| chr3:3175301
|
A | C | 1 | a0001c0001t0005g0051 | 2 | HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.68-32T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175301 | ||||||
| chr3:3175351
|
G | A | 10 | a0001c0001t0002g0170a0001c0001t0005g0014a0001c0001t0005g0023others(7): Show | 20 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-82C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175351 | ||||||
| chr3:3175444
|
AT | A | 161 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(158): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.68-176delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175444 | ||||||
| chr3:3175780
|
C | A | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.68-511G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175780 | ||||||
| chr3:3175788
|
G | C | 14 | a0001c0001t0003g0111a0001c0001t0010g0060a0001c0001t0010g0099others(11): Show | 23 | HG00280.hp2 HG00609.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-519C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175788 | ||||||
| chr3:3175887
|
CT | C | 2 | a0001c0001t0003g0111a0001c0001t0013g0041 | 3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68-619delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175887 | ||||||
| chr3:3175993
|
C | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.68-724G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175993 | ||||||
| chr3:3175998
|
G | C | 3 | a0001c0001t0010g0099a0001c0001t0010g0112a0001c0001t0010g0113 | 3 | HG00280.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.68-729C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175998 | ||||||
| chr3:3176006
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035 | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-737G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176006 | ||||||
| chr3:3176065
|
G | C | 1 | a0002c0005t0003g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68-796C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176065 | ||||||
| chr3:3176089
|
C | T | 1 | a0001c0001t0003g0030 | 2 | HG01109.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.68-820G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176089 | ||||||
| chr3:3176244
|
A | C | 68 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(65): Show | 147 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.68-975T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176244 | ||||||
| chr3:3176321
|
A | T | 1 | a0001c0002t0001g0115 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.68-1052T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176321 | ||||||
| chr3:3176345
|
A | C | 1 | a0001c0002t0001g0114 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-1076T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176345 | ||||||
| chr3:3176382
|
G | A | 1 | a0001c0001t0002g0053 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.68-1113C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176382 | ||||||
| chr3:3176412
|
GACA | G | 3 | a0001c0001t0010g0099a0001c0001t0010g0112a0001c0001t0010g0113 | 3 | HG00280.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.68-1146_68-1144del others(3): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176412 | ||||||
| chr3:3176558
|
C | A | 2 | a0001c0004t0002g0025a0001c0004t0002g0091 | 4 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1289G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176558 | ||||||
| chr3:3176593
|
G | A | 2 | a0001c0001t0003g0111a0001c0001t0013g0041 | 3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68-1324C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176593 | ||||||
| chr3:3176607
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.68-1338C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176607 | ||||||
| chr3:3176715
|
G | A | 2 | a0001c0001t0003g0015a0001c0001t0003g0079 | 6 | HG00438.hp1 HG02155.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1446C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176715 | ||||||
| chr3:3176799
|
A | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.68-1530T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176799 | ||||||
| chr3:3176853
|
C | T | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-1584G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176853 | ||||||
| chr3:3177007
|
G | C | 1 | a0001c0001t0002g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-1738C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177007 | ||||||
| chr3:3177009
|
G | T | 1 | a0001c0001t0002g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-1740C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177009 | ||||||
| chr3:3177147
|
G | GA | 29 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0002g0174others(26): Show | 54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.68-1879dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177147 | ||||||
| chr3:3177501
|
T | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+2120A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177501 | ||||||
| chr3:3177644
|
T | C | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+1977A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177644 | ||||||
| chr3:3177732
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.67+1889A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177732 | ||||||
| chr3:3177737
|
T | C | 8 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0059others(5): Show | 16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+1884A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177737 | ||||||
| chr3:3177793
|
A | G | 5 | a0001c0001t0001g0037a0001c0001t0003g0081a0001c0001t0012g0035others(2): Show | 9 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+1828T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177793 | ||||||
| chr3:3177827
|
T | C | 3 | a0001c0001t0010g0099a0001c0001t0010g0112a0001c0001t0010g0113 | 3 | HG00280.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.67+1794A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177827 | ||||||
| chr3:3177981
|
C | T | 166 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0037others(163): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.67+1640G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177981 | ||||||
| chr3:3178016
|
AC | A | 54 | a0001c0001t0005g0145a0001c0002t0001g0001a0001c0002t0001g0003others(51): Show | 124 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.67+1604delG | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178016 | ||||||
| chr3:3178017
|
C | CA | 26 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0002g0173others(23): Show | 51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+1603dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178017 | ||||||
| chr3:3178017
|
CA | C | 3 | a0001c0001t0010g0099a0001c0003t0007g0008a0001c0003t0007g0055 | 9 | HG00609.hp2 HG02165.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+1603delT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178017 | ||||||
| chr3:3178019
|
A | C | 1 | a0001c0002t0001g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+1602T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178019 | ||||||
| chr3:3178027
|
A | C | 1 | a0001c0003t0003g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.67+1594T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178027 | ||||||
| chr3:3178048
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+1573G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178048 | ||||||
| chr3:3178058
|
C | G | 1 | a0001c0004t0009g0097 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.67+1563G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178058 | ||||||
| chr3:3178094
|
G | A | 1 | a0001c0001t0001g0021 | 4 | HG00597.hp1 HG02738.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1527C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178094 | ||||||
| chr3:3178202
|
T | C | 6 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0059others(3): Show | 14 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+1419A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178202 | ||||||
| chr3:3178394
|
T | C | 1 | a0001c0001t0005g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.67+1227A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178394 | ||||||
| chr3:3178450
|
A | AC | 31 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0003g0004others(28): Show | 57 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.67+1170dupG | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178450 | ||||||
| chr3:3178540
|
T | C | 1 | a0001c0001t0001g0037 | 2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+1081A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178540 | ||||||
| chr3:3178705
|
C | A | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+916G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178705 | ||||||
| chr3:3178714
|
A | T | 1 | a0001c0001t0010g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.67+907T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178714 | ||||||
| chr3:3178720
|
C | A | 1 | a0001c0001t0004g0029 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+901G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178720 | ||||||
| chr3:3178734
|
T | G | 30 | a0001c0001t0002g0063a0001c0001t0002g0076a0001c0001t0003g0004others(27): Show | 55 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.67+887A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178734 | ||||||
| chr3:3178750
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.67+871C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178750 | ||||||
| chr3:3178789
|
G | C | 25 | a0001c0001t0002g0076a0001c0001t0003g0004a0001c0001t0003g0015others(22): Show | 50 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.67+832C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178789 | ||||||
| chr3:3178804
|
A | G | 1 | a0001c0002t0001g0096 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.67+817T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178804 | ||||||
| chr3:3178805
|
T | C | 53 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(50): Show | 121 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.67+816A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178805 | ||||||
| chr3:3178887
|
A | C | 163 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(160): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.67+734T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178887 | ||||||
| chr3:3178887
|
A | T | 1 | a0001c0001t0005g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.67+734T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178887 | ||||||
| chr3:3178950
|
G | C | 129 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(126): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.67+671C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178950 | ||||||
| chr3:3179045
|
G | C | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+576C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179045 | ||||||
| chr3:3179067
|
G | T | 1 | a0001c0002t0001g0093 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.67+554C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179067 | ||||||
| chr3:3179201
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+420A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179201 | ||||||
| chr3:3179318
|
G | C | 1 | a0001c0002t0001g0178 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.67+303C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179318 | ||||||
| chr3:3179339
|
CT | C | 3 | a0001c0001t0002g0092a0001c0004t0002g0025a0001c0004t0002g0091 | 5 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+281delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179339 | ||||||
| chr3:3179343
|
G | C | 1 | a0001c0001t0002g0054 | 2 | HG02135.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.67+278C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179343 | ||||||
| chr3:3179376
|
G | A | 124 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0039others(121): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.67+245C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179376 | ||||||
| chr3:3179414
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67+207T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179414 | ||||||
| chr3:3179443
|
A | G | 1 | a0001c0002t0001g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.67+178T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179443 | ||||||
| chr3:3179527
|
C | T | 1 | a0001c0002t0008g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.67+94G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179527 | ||||||
| chr3:3179544
|
C | T | 2 | a0001c0003t0007g0008a0001c0003t0007g0055 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+77G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179544 |