Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 923 |
|---|---|
| ensemblid | ENSG00000013725.14 |
| hgncid | 1691 |
| symbol | CD6 |
| name | CD6 molecule |
| refseq_nuc | NM_006725.5 |
| refseq_prot | NP_006716.3 |
| ensembl_nuc | ENST00000313421.11 |
| ensembl_prot | ENSP00000323280.7 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 60971680 |
| end | 61020377 |
| strand | + |
| ver | v1.2 |
| region | chr11:60971680-61020377 |
| region5000 | chr11:60966680-61025377 |
| regionname0 | CD6_chr11_60971680_61020377 |
| regionname5000 | CD6_chr11_60966680_61025377 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 668 | 112 | 30 | 17 | 48 | 6 | 10 | 32 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002 | 0/0 | 668 | 90 | 46 | 18 | 17 | 1 | 8 | 11 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003 | 0/0 | 668 | 31 | 6 | 1 | 17 | 0 | 7 | 11 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0004 | 0/1 | 668 | 27 | 4 | 14 | 0 | 3 | 5 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0005 | 0/0 | 668 | 21 | 1 | 12 | 3 | 1 | 4 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0006 | 0/0 | 668 | 8 | 0 | 0 | 6 | 0 | 2 | 4 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0007 | 0/0 | 668 | 5 | 1 | 2 | 0 | 0 | 2 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0008 | 0/0 | 668 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0009 | 0/0 | 668 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0010 | 0/0 | 668 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0011 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0012 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0013 | 0/0 | 668 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2007 | 84 | 6 | 15 | 47 | 6 | 9 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0002 | 0/0 | 2007 | 43 | 24 | 4 | 14 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0003 | 0/0 | 2007 | 41 | 17 | 14 | 3 | 1 | 6 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0004 | 0/1 | 2007 | 27 | 4 | 14 | 0 | 3 | 5 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0005 | 0/0 | 2007 | 26 | 1 | 1 | 17 | 0 | 7 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0006 | 0/0 | 2007 | 21 | 1 | 12 | 3 | 1 | 4 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0007 | 0/0 | 2007 | 20 | 20 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0008 | 0/0 | 2007 | 8 | 0 | 0 | 6 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0009 | 0/0 | 2007 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0010 | 0/0 | 2007 | 5 | 4 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0011 | 0/0 | 2007 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0012 | 0/0 | 2007 | 5 | 1 | 2 | 0 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0013 | 0/0 | 2007 | 3 | 0 | 0 | 3 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0014 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0015 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0016 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0017 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0018 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0019 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0020 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0021 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| c0022 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1246 | 277 | 72 | 61 | 93 | 12 | 37 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0002 | 0/0 | 1246 | 6 | 5 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0003 | 0/0 | 1246 | 3 | 1 | 1 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0004 | 0/0 | 1246 | 3 | 3 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0005 | 0/0 | 1246 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0006 | 0/0 | 1246 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0007 | 0/0 | 1246 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0008 | 0/0 | 1246 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0009 | 0/0 | 1246 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0010 | 0/0 | 1246 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0011 | 0/0 | 1246 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0012 | 0/0 | 1246 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0013 | 0/0 | 1246 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| t0014 | 0/0 | 1246 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0003 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2007 | 84 | 6 | 15 | 47 | 6 | 9 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0007 | 0/0 | 2007 | 20 | 20 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0010 | 0/0 | 2007 | 5 | 4 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0014 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0018 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0019 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0002 | 0/0 | 2007 | 43 | 24 | 4 | 14 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0003 | 0/0 | 2007 | 41 | 17 | 14 | 3 | 1 | 6 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0009 | 0/0 | 2007 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0016 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003c0005 | 0/0 | 2007 | 26 | 1 | 1 | 17 | 0 | 7 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003c0011 | 0/0 | 2007 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0004c0004 | 0/1 | 2007 | 27 | 4 | 14 | 0 | 3 | 5 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0005c0006 | 0/0 | 2007 | 21 | 1 | 12 | 3 | 1 | 4 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0006c0008 | 0/0 | 2007 | 8 | 0 | 0 | 6 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0007c0012 | 0/0 | 2007 | 5 | 1 | 2 | 0 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0008c0013 | 0/0 | 2007 | 3 | 0 | 0 | 3 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0009c0022 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0010c0020 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0011c0015 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0012c0017 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0013c0021 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3252 | 79 | 3 | 14 | 46 | 6 | 9 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0001t0007 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0001t0008 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0001t0009 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0001t0011 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0007t0001 | 0/0 | 3252 | 15 | 15 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0007t0002 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0007t0005 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0007t0006 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0007t0012 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0010t0002 | 0/0 | 3252 | 5 | 4 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0014t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0018t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0001c0019t0013 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0002t0001 | 0/0 | 3252 | 42 | 23 | 4 | 14 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0002t0014 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0003t0001 | 0/0 | 3252 | 41 | 17 | 14 | 3 | 1 | 6 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0009t0001 | 0/0 | 3252 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0002c0016t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003c0005t0001 | 0/0 | 3252 | 26 | 1 | 1 | 17 | 0 | 7 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003c0011t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003c0011t0004 | 0/0 | 3252 | 3 | 3 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0003c0011t0005 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0004c0004t0001 | 0/1 | 3252 | 27 | 4 | 14 | 0 | 3 | 5 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0005c0006t0001 | 0/0 | 3252 | 21 | 1 | 12 | 3 | 1 | 4 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0006c0008t0001 | 0/0 | 3252 | 8 | 0 | 0 | 6 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0007c0012t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0007c0012t0003 | 0/0 | 3252 | 3 | 1 | 1 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0007c0012t0010 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0008c0013t0001 | 0/0 | 3252 | 3 | 0 | 0 | 3 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0009c0022t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0010c0020t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0011c0015t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0012c0017t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| a0013c0021t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | copy fasta | chr11 | 60966680 | 61025377 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0014t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0018t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0019t0013g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0009t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0009t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0009t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0016t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0008c0013t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0008c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0008c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0009c0022t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0010c0020t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0011c0015t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0012c0017t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0013c0021t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0011 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00140 | hp2 | a0005 | c0006 | t0001 | g0122 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00323 | hp1 | a0004 | c0004 | t0001 | g0167 | EUR | FIN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00323 | hp2 | a0013 | c0021 | t0001 | g0129 | EUR | FIN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00408 | hp1 | a0003 | c0005 | t0001 | g0085 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0100 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00639 | hp1 | a0005 | c0006 | t0001 | g0032 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0274 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00673 | hp1 | a0006 | c0008 | t0001 | g0074 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0242 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01069 | hp2 | a0004 | c0004 | t0001 | g0015 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01070 | hp2 | a0004 | c0004 | t0001 | g0015 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0204 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01081 | hp1 | a0007 | c0012 | t0003 | g0033 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0243 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01099 | hp2 | a0005 | c0006 | t0001 | g0200 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01106 | hp2 | a0005 | c0006 | t0001 | g0123 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01109 | hp2 | a0001 | c0010 | t0002 | g0133 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0246 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01168 | hp1 | a0005 | c0006 | t0001 | g0276 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01168 | hp2 | a0004 | c0004 | t0001 | g0192 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01169 | hp1 | a0005 | c0006 | t0001 | g0277 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01175 | hp1 | a0004 | c0004 | t0001 | g0076 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01192 | hp1 | a0003 | c0005 | t0001 | g0087 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01192 | hp2 | a0004 | c0004 | t0001 | g0237 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0021 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01255 | hp2 | a0005 | c0006 | t0001 | g0193 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01256 | hp1 | a0005 | c0006 | t0001 | g0244 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0218 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01258 | hp2 | a0005 | c0006 | t0001 | g0245 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0039 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01261 | hp2 | a0005 | c0006 | t0001 | g0012 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0219 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01346 | hp2 | a0004 | c0004 | t0001 | g0018 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01358 | hp1 | a0001 | c0018 | t0001 | g0149 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0018 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01361 | hp1 | a0007 | c0012 | t0001 | g0035 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01433 | hp1 | a0005 | c0006 | t0001 | g0089 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0222 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01496 | hp2 | a0004 | c0004 | t0001 | g0077 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01515 | hp2 | a0004 | c0004 | t0001 | g0272 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01517 | hp2 | a0004 | c0004 | t0001 | g0270 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0278 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0217 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01943 | hp1 | a0004 | c0004 | t0001 | g0168 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0269 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02004 | hp1 | a0004 | c0004 | t0001 | g0206 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02004 | hp2 | a0005 | c0006 | t0001 | g0008 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02055 | hp1 | a0004 | c0004 | t0001 | g0111 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02055 | hp2 | a0004 | c0004 | t0001 | g0281 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02056 | hp1 | a0003 | c0005 | t0001 | g0099 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02074 | hp2 | a0005 | c0006 | t0001 | g0117 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02080 | hp2 | a0006 | c0008 | t0001 | g0249 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02083 | hp2 | a0003 | c0005 | t0001 | g0009 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02145 | hp2 | a0003 | c0011 | t0004 | g0045 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02165 | hp1 | a0005 | c0006 | t0001 | g0008 | EAS | CDX | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02165 | hp2 | a0003 | c0005 | t0001 | g0164 | EAS | CDX | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02257 | hp1 | a0001 | c0007 | t0001 | g0257 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0135 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0265 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02258 | hp2 | a0003 | c0011 | t0001 | g0227 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0231 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02293 | hp2 | a0004 | c0004 | t0001 | g0161 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02300 | hp1 | a0004 | c0004 | t0001 | g0271 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02572 | hp1 | a0001 | c0007 | t0001 | g0248 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02602 | hp1 | a0004 | c0004 | t0001 | g0201 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02602 | hp2 | a0005 | c0006 | t0001 | g0118 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02615 | hp1 | a0002 | c0009 | t0001 | g0024 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0247 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02622 | hp1 | a0004 | c0004 | t0001 | g0210 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02622 | hp2 | a0002 | c0009 | t0001 | g0023 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02630 | hp2 | a0002 | c0002 | t0014 | g0238 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0022 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02683 | hp1 | a0006 | c0008 | t0001 | g0063 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02698 | hp1 | a0003 | c0005 | t0001 | g0207 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0216 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02717 | hp1 | a0001 | c0010 | t0002 | g0014 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02738 | hp2 | a0005 | c0006 | t0001 | g0028 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0240 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02818 | hp1 | a0001 | c0007 | t0001 | g0020 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02886 | hp1 | a0001 | c0007 | t0001 | g0017 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02895 | hp1 | a0001 | c0010 | t0002 | g0235 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02895 | hp2 | a0001 | c0007 | t0006 | g0130 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0081 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02897 | hp1 | a0001 | c0007 | t0006 | g0131 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02965 | hp1 | a0002 | c0009 | t0001 | g0001 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0233 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02970 | hp2 | a0002 | c0009 | t0001 | g0001 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02976 | hp1 | a0001 | c0007 | t0001 | g0017 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03017 | hp1 | a0010 | c0020 | t0001 | g0042 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03017 | hp2 | a0006 | c0008 | t0001 | g0139 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03041 | hp1 | a0001 | c0007 | t0001 | g0252 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0041 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0220 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0268 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03130 | hp1 | a0001 | c0010 | t0002 | g0234 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03195 | hp2 | a0001 | c0007 | t0005 | g0275 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03209 | hp2 | a0011 | c0015 | t0001 | g0280 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03225 | hp1 | a0003 | c0011 | t0004 | g0279 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03225 | hp2 | a0001 | c0007 | t0001 | g0228 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0036 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03453 | hp2 | a0003 | c0011 | t0004 | g0044 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0236 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03486 | hp2 | a0001 | c0007 | t0012 | g0016 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0068 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03492 | hp1 | a0004 | c0004 | t0001 | g0005 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0066 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0267 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0260 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03579 | hp1 | a0001 | c0007 | t0001 | g0266 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0005 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03669 | hp1 | a0003 | c0005 | t0001 | g0043 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03669 | hp2 | a0003 | c0005 | t0001 | g0092 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0124 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03704 | hp2 | a0009 | c0022 | t0001 | g0213 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03831 | hp2 | a0005 | c0006 | t0001 | g0086 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03834 | hp1 | a0005 | c0006 | t0001 | g0114 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03927 | hp1 | a0002 | c0016 | t0001 | g0116 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03927 | hp2 | a0003 | c0005 | t0001 | g0027 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03942 | hp1 | a0007 | c0012 | t0010 | g0029 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03942 | hp2 | a0004 | c0004 | t0001 | g0067 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04184 | hp2 | a0003 | c0005 | t0001 | g0162 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0183 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04204 | hp1 | a0003 | c0005 | t0001 | g0126 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0030 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04228 | hp1 | a0003 | c0005 | t0001 | g0078 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18522 | hp2 | a0001 | c0007 | t0001 | g0046 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18747 | hp2 | a0003 | c0005 | t0001 | g0185 | EAS | CHB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18940 | hp1 | a0008 | c0013 | t0001 | g0112 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18946 | hp1 | a0003 | c0005 | t0001 | g0009 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0169 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18949 | hp2 | a0003 | c0005 | t0001 | g0056 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18951 | hp1 | a0005 | c0006 | t0001 | g0159 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18952 | hp1 | a0006 | c0008 | t0001 | g0184 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18952 | hp2 | a0001 | c0014 | t0001 | g0155 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18960 | hp2 | a0003 | c0005 | t0001 | g0165 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18975 | hp1 | a0003 | c0005 | t0001 | g0250 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18977 | hp2 | a0006 | c0008 | t0001 | g0119 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18982 | hp2 | a0003 | c0005 | t0001 | g0115 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18990 | hp1 | a0003 | c0005 | t0001 | g0160 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18994 | hp1 | a0003 | c0005 | t0001 | g0107 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0163 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19007 | hp1 | a0008 | c0013 | t0001 | g0145 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0221 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19030 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0224 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19043 | hp2 | a0001 | c0010 | t0002 | g0014 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19057 | hp2 | a0003 | c0005 | t0001 | g0253 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19063 | hp2 | a0003 | c0005 | t0001 | g0187 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19068 | hp1 | a0006 | c0008 | t0001 | g0075 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19081 | hp1 | a0006 | c0008 | t0001 | g0166 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19085 | hp1 | a0003 | c0005 | t0001 | g0172 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19088 | hp1 | a0008 | c0013 | t0001 | g0143 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19240 | hp2 | a0001 | c0007 | t0002 | g0258 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20129 | hp1 | a0003 | c0011 | t0005 | g0047 | AFR | ASW | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20129 | hp2 | a0004 | c0004 | t0001 | g0049 | AFR | ASW | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20905 | hp1 | a0001 | c0019 | t0013 | g0137 | SAS | GIH | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20905 | hp2 | a0007 | c0012 | t0003 | g0031 | SAS | GIH | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01123 | hp1 | a0005 | c0006 | t0001 | g0012 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01123 | hp2 | a0004 | c0004 | t0001 | g0120 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02109 | hp1 | a0007 | c0012 | t0003 | g0034 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02486 | hp1 | a0003 | c0005 | t0001 | g0230 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0214 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0020 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG06807 | hp2 | a0002 | c0009 | t0001 | g0001 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0232 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA21309 | hp1 | a0012 | c0017 | t0001 | g0215 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0004 | t0001 | g0273 | REF | REF | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61007755
|
C | T | 2 | a0007a0009 | 6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
missense_variant | MODERATE | c.314C>T | p.Pro105Leu | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/13 | 500/3252 | 314/2007 | 105/668 | chr11 | 61007755 | ||
| chr11:61007889
|
C | T | 1 | a0013 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.448C>T | p.Arg150Trp | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/13 | 634/3252 | 448/2007 | 150/668 | chr11 | 61007889 | ||
| chr11:61008714
|
C | T | 2 | a0005a0010 | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
missense_variant | MODERATE | c.650C>T | p.Thr217Met | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 836/3252 | 650/2007 | 217/668 | chr11 | 61008714 | ||
| chr11:61008737
|
C | T | 4 | a0002a0004a0011others(1): Show | 119 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(116): Show |
missense_variant | MODERATE | c.673C>T | p.Arg225Trp | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 859/3252 | 673/2007 | 225/668 | chr11 | 61008737 | ||
| chr11:61008834
|
C | T | 8 | a0002a0003a0004others(5): Show | 180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
missense_variant | MODERATE | c.770C>T | p.Ala257Val | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 956/3252 | 770/2007 | 257/668 | chr11 | 61008834 | ||
| chr11:61009601
|
G | A | 1 | a0004 | 27 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
missense_variant | MODERATE | c.811G>A | p.Ala271Thr | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/13 | 997/3252 | 811/2007 | 271/668 | chr11 | 61009601 | ||
| chr11:61015767
|
G | A | 1 | a0011 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1442G>A | p.Gly481Asp | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/13 | 1628/3252 | 1442/2007 | 481/668 | chr11 | 61015767 | ||
| chr11:61017791
|
A | G | 1 | a0007 | 5 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(2): Show |
missense_variant | MODERATE | c.1615A>G | p.Thr539Ala | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 1801/3252 | 1615/2007 | 539/668 | chr11 | 61017791 | ||
| chr11:61017992
|
G | A | 4 | a0005a0006a0008others(1): Show | 33 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(30): Show |
missense_variant | MODERATE | c.1816G>A | p.Gly606Ser | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 2002/3252 | 1816/2007 | 606/668 | chr11 | 61017992 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61007774
|
G | A | 1 | a0001c0014 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.333G>A | p.Gly111Gly | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/13 | 519/3252 | 333/2007 | 111/668 | chr11 | 61007774 | ||
| chr11:61008631
|
T | C | 5 | a0002c0003a0002c0009a0002c0016others(2): Show | 49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
synonymous_variant | LOW | c.567T>C | p.Thr189Thr | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 753/3252 | 567/2007 | 189/668 | chr11 | 61008631 | ||
| chr11:61008718
|
C | T | 1 | a0001c0019 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.654C>T | p.Pro218Pro | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 840/3252 | 654/2007 | 218/668 | chr11 | 61008718 | ||
| chr11:61008835
|
G | C | 5 | a0002c0003a0002c0009a0002c0016others(2): Show | 49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
synonymous_variant | LOW | c.771G>C | p.Ala257Ala | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 957/3252 | 771/2007 | 257/668 | chr11 | 61008835 | ||
| chr11:61009573
|
G | A | 1 | a0001c0010 | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.783G>A | p.Glu261Glu | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/13 | 969/3252 | 783/2007 | 261/668 | chr11 | 61009573 | ||
| chr11:61017841
|
G | A | 1 | a0001c0018 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1665G>A | p.Gln555Gln | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 1851/3252 | 1665/2007 | 555/668 | chr11 | 61017841 | ||
| chr11:61017880
|
A | G | 13 | a0001c0007a0001c0010a0002c0003others(10): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
synonymous_variant | LOW | c.1704A>G | p.Ser568Ser | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 1890/3252 | 1704/2007 | 568/668 | chr11 | 61017880 | ||
| chr11:61017991
|
C | T | 2 | a0002c0009a0004c0004 | 32 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(29): Show |
synonymous_variant | LOW | c.1815C>T | p.Ala605Ala | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 2001/3252 | 1815/2007 | 605/668 | chr11 | 61017991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61019432
|
C | T | 1 | a0002c0002t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 114 | chr11 | 61019432 | |||||
| chr11:61019465
|
T | C | 1 | a0001c0001t0008 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 147 | chr11 | 61019465 | |||||
| chr11:61019685
|
G | A | 1 | a0001c0001t0009 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 367 | chr11 | 61019685 | |||||
| chr11:61019737
|
G | A | 2 | a0007c0012t0003a0007c0012t0010 | 4 | HG01081.hp1 HG02109.hp1 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*419G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 419 | chr11 | 61019737 | |||||
| chr11:61019823
|
C | T | 1 | a0001c0019t0013 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 505 | chr11 | 61019823 | |||||
| chr11:61019832
|
G | C | 2 | a0001c0007t0005a0003c0011t0005 | 2 | HG03195.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 514 | chr11 | 61019832 | |||||
| chr11:61019854
|
C | T | 2 | a0001c0007t0012a0003c0011t0004 | 4 | HG02145.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 536 | chr11 | 61019854 | |||||
| chr11:61019873
|
G | A | 2 | a0001c0007t0002a0001c0010t0002 | 6 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*555G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 555 | chr11 | 61019873 | |||||
| chr11:61020031
|
A | G | 1 | a0007c0012t0010 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*713A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 713 | chr11 | 61020031 | |||||
| chr11:61020180
|
G | A | 1 | a0001c0007t0012 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 862 | chr11 | 61020180 | |||||
| chr11:61020204
|
T | G | 1 | a0001c0007t0006 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*886T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 886 | chr11 | 61020204 | |||||
| chr11:61020268
|
G | A | 1 | a0001c0001t0011 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*950G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 950 | chr11 | 61020268 | |||||
| chr11:61020280
|
G | A | 1 | a0001c0001t0007 | 2 | HG02630.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*962G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 962 | chr11 | 61020280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:60971922
|
C | T | 1 | a0004c0004t0001g0281 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.49+8C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60971922 | ||||||
| chr11:60971969
|
C | T | 3 | a0001c0001t0011g0278a0003c0011t0004g0279a0011c0015t0001g0280 | 3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.49+55C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60971969 | ||||||
| chr11:60972084
|
A | T | 1 | a0001c0007t0001g0020 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+170A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972084 | ||||||
| chr11:60972215
|
G | C | 3 | a0002c0003t0001g0002a0002c0003t0001g0021a0002c0003t0001g0022 | 4 | HG01243.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+301G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972215 | ||||||
| chr11:60972279
|
A | G | 261 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.49+365A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972279 | ||||||
| chr11:60972291
|
G | A | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+377G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972291 | ||||||
| chr11:60972360
|
T | G | 275 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(272): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.49+446T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972360 | ||||||
| chr11:60972476
|
G | A | 1 | a0002c0003t0001g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.49+562G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972476 | ||||||
| chr11:60972584
|
C | G | 1 | a0001c0001t0001g0019 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.49+670C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972584 | ||||||
| chr11:60972787
|
G | C | 9 | a0002c0003t0001g0030a0003c0005t0001g0027a0005c0006t0001g0028others(6): Show | 9 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+873G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972787 | ||||||
| chr11:60972795
|
G | A | 1 | a0010c0020t0001g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+881G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972795 | ||||||
| chr11:60972827
|
A | T | 9 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0270others(6): Show | 10 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+913A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972827 | ||||||
| chr11:60972832
|
G | A | 1 | a0003c0005t0001g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+918G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972832 | ||||||
| chr11:60972863
|
C | T | 1 | a0001c0001t0008g0269 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.49+949C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972863 | ||||||
| chr11:60973063
|
G | A | 1 | a0003c0005t0001g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+1149G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973063 | ||||||
| chr11:60973143
|
A | G | 34 | a0001c0001t0001g0254a0001c0001t0001g0261a0001c0001t0007g0259others(31): Show | 36 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.49+1229A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973143 | ||||||
| chr11:60973181
|
C | A | 196 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(193): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.49+1267C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973181 | ||||||
| chr11:60973294
|
G | C | 5 | a0001c0007t0001g0020a0001c0007t0001g0046a0003c0011t0004g0044others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+1380G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973294 | ||||||
| chr11:60973305
|
A | G | 1 | a0002c0003t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+1391A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973305 | ||||||
| chr11:60973385
|
C | T | 1 | a0002c0003t0001g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+1471C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973385 | ||||||
| chr11:60973539
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.49+1625T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973539 | ||||||
| chr11:60973572
|
CAT | C | 10 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0049others(7): Show | 11 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+1660_49+1661del others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60973572 | |||||
| chr11:60973584
|
T | C | 1 | a0004c0004t0001g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49+1670T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973584 | ||||||
| chr11:60973779
|
G | A | 1 | a0003c0011t0004g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+1865G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973779 | ||||||
| chr11:60974020
|
A | G | 1 | a0002c0002t0001g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+2106A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974020 | ||||||
| chr11:60974234
|
G | A | 4 | a0001c0007t0001g0020a0001c0007t0001g0046a0003c0011t0004g0044others(1): Show | 5 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2320G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974234 | ||||||
| chr11:60974314
|
C | G | 1 | a0001c0007t0001g0020 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+2400C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974314 | ||||||
| chr11:60974355
|
G | A | 7 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0052others(4): Show | 7 | HG03704.hp2 HG03834.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+2441G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974355 | ||||||
| chr11:60974383
|
A | G | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+2469A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974383 | ||||||
| chr11:60974443
|
C | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+2529C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974443 | ||||||
| chr11:60974449
|
G | A | 1 | a0002c0003t0001g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.49+2535G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974449 | ||||||
| chr11:60974530
|
C | G | 2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+2616C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974530 | ||||||
| chr11:60974566
|
T | C | 2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+2652T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974566 | ||||||
| chr11:60974809
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49+2895G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974809 | ||||||
| chr11:60974812
|
T | C | 1 | a0002c0002t0001g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49+2898T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974812 | ||||||
| chr11:60974827
|
C | T | 1 | a0007c0012t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.49+2913C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974827 | ||||||
| chr11:60975124
|
ATATTT | A | 236 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(233): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.49+3219_49+3223del others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60975124 | |||||
| chr11:60975133
|
TTTA | T | 4 | a0001c0007t0001g0020a0001c0007t0001g0046a0003c0011t0004g0044others(1): Show | 5 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3221_49+3223del others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60975133 | |||||
| chr11:60975166
|
C | T | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+3252C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975166 | ||||||
| chr11:60975316
|
A | G | 240 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(237): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.49+3402A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975316 | ||||||
| chr11:60975424
|
G | A | 10 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0049others(7): Show | 11 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+3510G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975424 | ||||||
| chr11:60975627
|
C | G | 4 | a0001c0007t0001g0020a0001c0007t0001g0046a0003c0011t0004g0044others(1): Show | 5 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3713C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975627 | ||||||
| chr11:60975767
|
T | G | 280 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(277): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.49+3853T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975767 | ||||||
| chr11:60975777
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.49+3863C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975777 | ||||||
| chr11:60975836
|
A | G | 1 | a0004c0004t0001g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49+3922A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975836 | ||||||
| chr11:60976081
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG00558.hp2 HG02129.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.49+4167C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976081 | ||||||
| chr11:60976103
|
A | G | 280 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(277): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.49+4189A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976103 | ||||||
| chr11:60976124
|
T | C | 28 | a0001c0001t0001g0013a0001c0001t0011g0278a0001c0007t0001g0220others(25): Show | 30 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+4210T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976124 | ||||||
| chr11:60976142
|
A | G | 1 | a0003c0005t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.49+4228A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976142 | ||||||
| chr11:60976172
|
C | T | 1 | a0004c0004t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49+4258C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976172 | ||||||
| chr11:60976198
|
A | C | 1 | a0001c0001t0001g0186 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.49+4284A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976198 | ||||||
| chr11:60976318
|
A | C | 11 | a0002c0003t0001g0026a0002c0003t0001g0030a0003c0005t0001g0027others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+4404A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976318 | ||||||
| chr11:60976323
|
T | C | 2 | a0004c0004t0001g0192a0005c0006t0001g0193 | 2 | HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.49+4409T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976323 | ||||||
| chr11:60976381
|
T | G | 240 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(237): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.49+4467T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976381 | ||||||
| chr11:60976467
|
G | A | 1 | a0003c0005t0001g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.49+4553G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976467 | ||||||
| chr11:60976485
|
C | T | 1 | a0007c0012t0003g0034 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+4571C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976485 | ||||||
| chr11:60976517
|
T | C | 1 | a0002c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49+4603T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976517 | ||||||
| chr11:60976586
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.49+4672G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976586 | ||||||
| chr11:60976646
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.49+4732T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976646 | ||||||
| chr11:60976752
|
G | A | 5 | a0002c0003t0001g0242a0002c0003t0001g0243a0002c0003t0001g0246others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+4838G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976752 | ||||||
| chr11:60976771
|
G | C | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+4857G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976771 | ||||||
| chr11:60976796
|
C | T | 13 | a0002c0002t0001g0025a0002c0003t0001g0030a0002c0009t0001g0001others(10): Show | 15 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+4882C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976796 | ||||||
| chr11:60977321
|
G | A | 9 | a0002c0003t0001g0030a0003c0005t0001g0027a0005c0006t0001g0028others(6): Show | 9 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5407G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977321 | ||||||
| chr11:60977414
|
T | C | 1 | a0004c0004t0001g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49+5500T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977414 | ||||||
| chr11:60977544
|
C | T | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+5630C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977544 | ||||||
| chr11:60977596
|
C | G | 160 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(157): Show | 166 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.49+5682C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977596 | ||||||
| chr11:60977675
|
G | A | 1 | a0001c0001t0001g0006 | 2 | NA18948.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.49+5761G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977675 | ||||||
| chr11:60977775
|
G | A | 7 | a0004c0004t0001g0018a0004c0004t0001g0049a0004c0004t0001g0270others(4): Show | 8 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+5861G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977775 | ||||||
| chr11:60978034
|
T | C | 4 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0071others(1): Show | 4 | HG01109.hp1 HG02886.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+6120T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978034 | ||||||
| chr11:60978086
|
A | G | 1 | a0003c0005t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.49+6172A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978086 | ||||||
| chr11:60978256
|
G | A | 1 | a0005c0006t0001g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+6342G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978256 | ||||||
| chr11:60978261
|
C | T | 1 | a0010c0020t0001g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+6347C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978261 | ||||||
| chr11:60978269
|
G | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6355G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978269 | ||||||
| chr11:60978295
|
C | T | 4 | a0002c0002t0001g0239a0002c0002t0014g0238a0002c0003t0001g0240others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+6381C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978295 | ||||||
| chr11:60978299
|
T | C | 8 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0049others(5): Show | 9 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+6385T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978299 | ||||||
| chr11:60978540
|
C | T | 2 | a0001c0007t0001g0266a0001c0007t0001g0267 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+6626C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978540 | ||||||
| chr11:60978874
|
A | G | 1 | a0006c0008t0001g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.49+6960A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978874 | ||||||
| chr11:60978875
|
T | C | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6961T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978875 | ||||||
| chr11:60978932
|
C | T | 3 | a0001c0007t0001g0046a0003c0011t0004g0044a0003c0011t0004g0045 | 3 | HG02145.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.49+7018C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978932 | ||||||
| chr11:60978986
|
C | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7072C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978986 | ||||||
| chr11:60979338
|
C | T | 8 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0049others(5): Show | 9 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+7424C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979338 | ||||||
| chr11:60979420
|
G | A | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 15 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+7506G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979420 | ||||||
| chr11:60979460
|
T | G | 1 | a0012c0017t0001g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+7546T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979460 | ||||||
| chr11:60979464
|
C | CT | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0007t0001g0020others(5): Show | 9 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+7564dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60979464 | |||||
| chr11:60979464
|
CT | C | 9 | a0001c0001t0001g0013a0002c0002t0001g0025a0002c0003t0001g0216others(6): Show | 12 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+7564delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60979464 | |||||
| chr11:60979549
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.49+7635C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979549 | ||||||
| chr11:60979592
|
G | A | 2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+7678G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979592 | ||||||
| chr11:60979657
|
G | A | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7743G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979657 | ||||||
| chr11:60979695
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.49+7781T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979695 | ||||||
| chr11:60979764
|
G | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(161): Show | 172 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.49+7850G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979764 | ||||||
| chr11:60979771
|
C | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7857C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979771 | ||||||
| chr11:60979871
|
G | A | 1 | a0004c0004t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49+7957G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979871 | ||||||
| chr11:60979901
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.49+7987C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979901 | ||||||
| chr11:60979938
|
C | T | 1 | a0002c0002t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.49+8024C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979938 | ||||||
| chr11:60980041
|
G | A | 2 | a0006c0008t0001g0074a0006c0008t0001g0184 | 2 | HG00673.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.49+8127G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980041 | ||||||
| chr11:60980047
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.49+8133G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980047 | ||||||
| chr11:60980253
|
A | G | 279 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(276): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.49+8339A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980253 | ||||||
| chr11:60980274
|
C | T | 2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+8360C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980274 | ||||||
| chr11:60980305
|
G | C | 254 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(251): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.49+8391G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980305 | ||||||
| chr11:60980327
|
A | AC | 158 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(155): Show | 164 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.49+8418dupC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60980327 | |||||
| chr11:60980327
|
A | ACC | 5 | a0001c0001t0001g0179a0002c0002t0001g0025a0002c0009t0001g0001others(2): Show | 7 | HG00423.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+8417_49+8418dup others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60980327 | |||||
| chr11:60980327
|
A | C | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8413A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980327 | ||||||
| chr11:60980507
|
A | G | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8593A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980507 | ||||||
| chr11:60980508
|
G | A | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8594G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980508 | ||||||
| chr11:60980508
|
GA | G | 65 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0261others(62): Show | 70 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.49+8604delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60980508 | |||||
| chr11:60980513
|
A | T | 1 | a0010c0020t0001g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+8599A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980513 | ||||||
| chr11:60980550
|
C | A | 7 | a0004c0004t0001g0018a0004c0004t0001g0049a0004c0004t0001g0270others(4): Show | 8 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+8636C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980550 | ||||||
| chr11:60980553
|
G | T | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8639G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980553 | ||||||
| chr11:60980766
|
G | C | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+8852G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980766 | ||||||
| chr11:60980797
|
ACCACTGC others(5): Show |
A | 11 | a0002c0003t0001g0026a0002c0003t0001g0030a0003c0005t0001g0027others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+8884_49+8895del others(12): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980797 | ||||||
| chr11:60980835
|
G | A | 1 | a0002c0003t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+8921G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980835 | ||||||
| chr11:60980876
|
C | T | 1 | a0001c0007t0005g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.49+8962C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980876 | ||||||
| chr11:60981186
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49+9272C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981186 | ||||||
| chr11:60981358
|
C | T | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+9444C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981358 | ||||||
| chr11:60981467
|
C | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(171): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.49+9553C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981467 | ||||||
| chr11:60981539
|
G | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0009g0176 | 3 | HG00558.hp1 HG02132.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.49+9625G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981539 | ||||||
| chr11:60981625
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.49+9711C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981625 | ||||||
| chr11:60981629
|
A | G | 5 | a0001c0001t0007g0040a0001c0010t0002g0014a0001c0010t0002g0234others(2): Show | 6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+9715A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981629 | ||||||
| chr11:60981704
|
C | G | 236 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(233): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.49+9790C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981704 | ||||||
| chr11:60981774
|
T | C | 34 | a0001c0001t0001g0254a0001c0001t0001g0261a0001c0001t0007g0259others(31): Show | 37 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+9860T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981774 | ||||||
| chr11:60981784
|
G | A | 58 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0261others(55): Show | 62 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.49+9870G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981784 | ||||||
| chr11:60981986
|
A | T | 8 | a0001c0001t0001g0013a0002c0003t0001g0216a0002c0003t0001g0217others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+10072A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981986 | ||||||
| chr11:60982002
|
C | G | 1 | a0002c0002t0001g0264 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.49+10088C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982002 | ||||||
| chr11:60982042
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.49+10128G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982042 | ||||||
| chr11:60982068
|
CG | C | 211 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(208): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.49+10165delG | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982068 | |||||
| chr11:60982088
|
A | G | 10 | a0002c0003t0001g0026a0002c0003t0001g0030a0003c0005t0001g0027others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+10174A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982088 | ||||||
| chr11:60982097
|
G | A | 5 | a0001c0001t0007g0040a0001c0007t0001g0046a0003c0011t0004g0044others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+10183G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982097 | ||||||
| chr11:60982112
|
C | G | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10198C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982112 | ||||||
| chr11:60982113
|
G | C | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10199G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982113 | ||||||
| chr11:60982123
|
C | CGGTCTGT others(44): Show |
1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10232_49+10233i others(53): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(44): Show |
1 | a0001c0001t0001g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.49+10232_49+10233i others(53): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(44): Show |
124 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(121): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(53): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(45): Show |
86 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0060others(83): Show | 91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(54): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(46): Show |
43 | a0001c0001t0001g0083a0001c0001t0001g0254a0001c0001t0011g0278others(40): Show | 44 | HG00423.hp2 HG00639.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(55): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(47): Show |
16 | a0001c0001t0001g0065a0001c0010t0002g0234a0001c0010t0002g0235others(13): Show | 17 | HG00639.hp1 HG01346.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(56): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(48): Show |
2 | a0001c0001t0001g0064a0001c0007t0005g0275 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49+10232_49+10233i others(57): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(46): Show |
1 | a0001c0007t0001g0020 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+10232_49+10233i others(55): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982123
|
C | CGGTCTGT others(43): Show |
1 | a0002c0002t0001g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+10232_49+10233i others(52): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | |||||
| chr11:60982125
|
G | GTCTGTGC others(45): Show |
5 | a0002c0003t0001g0242a0002c0003t0001g0243a0002c0003t0001g0246others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(54): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982125 | |||||
| chr11:60982219
|
T | C | 1 | a0003c0011t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+10305T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982219 | ||||||
| chr11:60982519
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+10605G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982519 | ||||||
| chr11:60982562
|
C | T | 1 | a0002c0003t0001g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+10648C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982562 | ||||||
| chr11:60982576
|
T | C | 245 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(242): Show | 259 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.49+10662T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982576 | ||||||
| chr11:60982653
|
C | T | 1 | a0002c0003t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+10739C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982653 | ||||||
| chr11:60982715
|
G | C | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+10801G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982715 | ||||||
| chr11:60982719
|
A | T | 1 | a0002c0003t0001g0219 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49+10805A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982719 | ||||||
| chr11:60982743
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.49+10829C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982743 | ||||||
| chr11:60982768
|
G | A | 240 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(237): Show | 253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.49+10854G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982768 | ||||||
| chr11:60982775
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0011g0278a0001c0007t0001g0228others(21): Show | 25 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.49+10861G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982775 | ||||||
| chr11:60982776
|
A | G | 1 | a0002c0002t0001g0054 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10862A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982776 | ||||||
| chr11:60982826
|
GTCTGCAG others(4): Show |
G | 245 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(242): Show | 259 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.49+10916_49+10926d others(13): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982826 | |||||
| chr11:60982964
|
G | T | 1 | a0001c0007t0001g0020 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+11050G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982964 | ||||||
| chr11:60983101
|
T | C | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+11187T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983101 | ||||||
| chr11:60983202
|
G | T | 255 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(252): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.49+11288G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983202 | ||||||
| chr11:60983247
|
C | A | 5 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0052others(2): Show | 5 | NA18949.hp1 NA18977.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+11333C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983247 | ||||||
| chr11:60983302
|
G | C | 2 | a0003c0005t0001g0043a0003c0005t0001g0126 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.49+11388G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983302 | ||||||
| chr11:60983394
|
T | C | 5 | a0001c0001t0007g0040a0001c0010t0002g0014a0001c0010t0002g0234others(2): Show | 6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+11480T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983394 | ||||||
| chr11:60983453
|
C | G | 8 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0049others(5): Show | 9 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+11539C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983453 | ||||||
| chr11:60983474
|
G | A | 1 | a0002c0003t0001g0222 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.49+11560G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983474 | ||||||
| chr11:60983505
|
A | G | 1 | a0002c0003t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+11591A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983505 | ||||||
| chr11:60983522
|
T | C | 11 | a0002c0003t0001g0030a0003c0005t0001g0027a0005c0006t0001g0028others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+11608T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983522 | ||||||
| chr11:60983636
|
T | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+11722T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983636 | ||||||
| chr11:60983805
|
G | A | 144 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(141): Show | 150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.49+11891G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983805 | ||||||
| chr11:60984087
|
T | G | 5 | a0001c0001t0007g0040a0001c0010t0002g0014a0001c0010t0002g0234others(2): Show | 6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+12173T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984087 | ||||||
| chr11:60984097
|
C | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(90): Show | 95 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.49+12183C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984097 | ||||||
| chr11:60984170
|
A | G | 69 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0261others(66): Show | 74 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.49+12256A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984170 | ||||||
| chr11:60984282
|
A | G | 1 | a0004c0004t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+12368A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984282 | ||||||
| chr11:60984330
|
G | A | 1 | a0003c0011t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+12416G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984330 | ||||||
| chr11:60984451
|
C | T | 252 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(249): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.49+12537C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984451 | ||||||
| chr11:60984500
|
G | A | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.49+12586G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984500 | ||||||
| chr11:60984534
|
G | A | 12 | a0001c0007t0005g0275a0002c0002t0001g0025a0002c0009t0001g0001others(9): Show | 15 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+12620G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984534 | ||||||
| chr11:60984710
|
T | C | 3 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235 | 4 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12796T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984710 | ||||||
| chr11:60984717
|
G | A | 4 | a0002c0003t0001g0059a0002c0003t0001g0066a0002c0003t0001g0124others(1): Show | 4 | HG00438.hp2 HG03492.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12803G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984717 | ||||||
| chr11:60984750
|
A | G | 2 | a0001c0014t0001g0155a0002c0002t0001g0156 | 2 | NA18952.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.49+12836A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984750 | ||||||
| chr11:60984799
|
T | A | 1 | a0001c0001t0001g0127 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.49+12885T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984799 | ||||||
| chr11:60984807
|
G | C | 13 | a0002c0003t0001g0026a0002c0003t0001g0030a0003c0005t0001g0027others(10): Show | 13 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+12893G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984807 | ||||||
| chr11:60985074
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.49+13160G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985074 | ||||||
| chr11:60985142
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+13228C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985142 | ||||||
| chr11:60985174
|
C | CT | 33 | a0001c0001t0001g0064a0001c0001t0001g0080a0001c0001t0001g0199others(30): Show | 38 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.49+13286dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | |||||
| chr11:60985174
|
C | CTT | 7 | a0001c0001t0001g0195a0001c0001t0001g0202a0002c0003t0001g0236others(4): Show | 7 | HG01175.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+13285_49+13286d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | |||||
| chr11:60985174
|
CT | C | 144 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(141): Show | 152 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.49+13286delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | |||||
| chr11:60985174
|
CTT | C | 11 | a0001c0001t0001g0090a0001c0001t0001g0128a0001c0001t0001g0157others(8): Show | 12 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+13285_49+13286d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | |||||
| chr11:60985223
|
G | A | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13309G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985223 | ||||||
| chr11:60985357
|
G | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+13443G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985357 | ||||||
| chr11:60985400
|
G | A | 1 | a0003c0005t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.49+13486G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985400 | ||||||
| chr11:60985504
|
T | C | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13590T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985504 | ||||||
| chr11:60985573
|
A | AAT | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+13671_49+13672d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985573 | |||||
| chr11:60985643
|
A | C | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13729A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985643 | ||||||
| chr11:60985681
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.49+13767G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985681 | ||||||
| chr11:60986018
|
C | T | 1 | a0012c0017t0001g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+14104C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986018 | ||||||
| chr11:60986051
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.49+14137C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986051 | ||||||
| chr11:60986244
|
C | T | 1 | a0002c0003t0001g0232 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49+14330C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986244 | ||||||
| chr11:60986296
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+14382T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986296 | ||||||
| chr11:60986468
|
A | G | 5 | a0001c0001t0001g0013a0002c0003t0001g0216a0002c0003t0001g0217others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+14554A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986468 | ||||||
| chr11:60986488
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+14574C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986488 | ||||||
| chr11:60986525
|
C | G | 5 | a0001c0001t0007g0040a0001c0010t0002g0014a0001c0010t0002g0234others(2): Show | 6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+14611C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986525 | ||||||
| chr11:60986614
|
T | C | 1 | a0001c0007t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.49+14700T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986614 | ||||||
| chr11:60986750
|
C | T | 4 | a0002c0003t0001g0059a0002c0003t0001g0066a0002c0003t0001g0124others(1): Show | 4 | HG00438.hp2 HG03492.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+14836C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986750 | ||||||
| chr11:60986781
|
T | C | 3 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235 | 4 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+14867T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986781 | ||||||
| chr11:60986836
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0191 | 2 | NA18946.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.49+14922G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986836 | ||||||
| chr11:60987001
|
G | A | 2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+15087G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987001 | ||||||
| chr11:60987013
|
G | A | 1 | a0002c0003t0001g0039 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.49+15099G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987013 | ||||||
| chr11:60987043
|
G | A | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+15129G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987043 | ||||||
| chr11:60987081
|
T | A | 2 | a0002c0003t0001g0021a0002c0003t0001g0041 | 2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.49+15167T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987081 | ||||||
| chr11:60987094
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0007t0001g0020 | 4 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+15180C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987094 | ||||||
| chr11:60987272
|
T | C | 4 | a0002c0003t0001g0059a0002c0003t0001g0066a0002c0003t0001g0124others(1): Show | 4 | HG00438.hp2 HG03492.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+15358T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987272 | ||||||
| chr11:60987312
|
G | A | 2 | a0004c0004t0001g0270a0004c0004t0001g0272 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.49+15398G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987312 | ||||||
| chr11:60987524
|
T | A | 1 | a0005c0006t0001g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.49+15610T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987524 | ||||||
| chr11:60987544
|
G | GGT | 8 | a0001c0007t0005g0275a0004c0004t0001g0018a0004c0004t0001g0049others(5): Show | 9 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+15641_49+15642d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60987544 | |||||
| chr11:60987545
|
G | GTGTGTGT others(11): Show |
4 | a0005c0006t0001g0028a0005c0006t0001g0032a0005c0006t0001g0244others(1): Show | 4 | HG00639.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+15635_49+15652d others(20): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60987545 | |||||
| chr11:60987723
|
A | AGAGAG | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15809_49+15810i others(7): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987723 | ||||||
| chr11:60987724
|
T | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15810T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987724 | ||||||
| chr11:60987725
|
C | A | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15811C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987725 | ||||||
| chr11:60987728
|
T | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15814T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987728 | ||||||
| chr11:60987729
|
T | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15815T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987729 | ||||||
| chr11:60987730
|
T | A | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15816T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987730 | ||||||
| chr11:60987731
|
C | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15817C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987731 | ||||||
| chr11:60987763
|
A | T | 3 | a0002c0002t0001g0225a0002c0002t0001g0226a0002c0002t0001g0229 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+15849A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987763 | ||||||
| chr11:60987779
|
C | T | 240 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(237): Show | 253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.49+15865C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987779 | ||||||
| chr11:60987862
|
A | G | 11 | a0002c0003t0001g0030a0003c0005t0001g0027a0005c0006t0001g0028others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+15948A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987862 | ||||||
| chr11:60987868
|
G | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+15954G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987868 | ||||||
| chr11:60987889
|
C | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+15975C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987889 | ||||||
| chr11:60987916
|
G | T | 3 | a0002c0002t0001g0225a0002c0002t0001g0226a0002c0002t0001g0229 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+16002G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987916 | ||||||
| chr11:60987947
|
A | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0173a0001c0001t0001g0182others(1): Show | 4 | HG02055.hp1 NA18747.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+16033A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987947 | ||||||
| chr11:60988012
|
G | A | 12 | a0001c0007t0005g0275a0002c0002t0001g0025a0002c0009t0001g0001others(9): Show | 15 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+16098G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988012 | ||||||
| chr11:60988045
|
A | G | 21 | a0001c0001t0001g0080a0001c0001t0001g0195a0001c0001t0001g0199others(18): Show | 24 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+16131A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988045 | ||||||
| chr11:60988478
|
AGAG | A | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+16569_49+16571d others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60988478 | |||||
| chr11:60988619
|
C | T | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+16705C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988619 | ||||||
| chr11:60988703
|
G | A | 141 | a0001c0001t0001g0019a0001c0001t0001g0048a0001c0001t0001g0057others(138): Show | 146 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.49+16789G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988703 | ||||||
| chr11:60988884
|
G | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0261others(66): Show | 74 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.49+16970G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988884 | ||||||
| chr11:60989116
|
C | T | 173 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(170): Show | 181 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.49+17202C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989116 | ||||||
| chr11:60989287
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.50-17287C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989287 | ||||||
| chr11:60989370
|
C | T | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-17204C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989370 | ||||||
| chr11:60989677
|
T | C | 1 | a0001c0001t0011g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.50-16897T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989677 | ||||||
| chr11:60989822
|
G | A | 11 | a0002c0003t0001g0030a0003c0005t0001g0027a0005c0006t0001g0028others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-16752G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989822 | ||||||
| chr11:60989953
|
A | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-16621A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989953 | ||||||
| chr11:60989959
|
C | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-16615C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989959 | ||||||
| chr11:60990005
|
T | A | 1 | a0013c0021t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.50-16569T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990005 | ||||||
| chr11:60990070
|
A | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(79): Show | 84 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.50-16504A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990070 | ||||||
| chr11:60990160
|
C | T | 4 | a0001c0007t0001g0220a0001c0007t0001g0224a0002c0002t0001g0223others(1): Show | 4 | HG01496.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-16414C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990160 | ||||||
| chr11:60990161
|
C | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0261others(66): Show | 74 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.50-16413C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990161 | ||||||
| chr11:60990255
|
C | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-16319C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990255 | ||||||
| chr11:60990293
|
C | T | 2 | a0001c0001t0001g0083a0002c0002t0001g0255 | 2 | NA18971.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.50-16281C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990293 | ||||||
| chr11:60990385
|
C | T | 143 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(140): Show | 149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.50-16189C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990385 | ||||||
| chr11:60990504
|
G | A | 2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.50-16070G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990504 | ||||||
| chr11:60990544
|
C | G | 1 | a0002c0003t0001g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-16030C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990544 | ||||||
| chr11:60990651
|
C | T | 3 | a0002c0003t0001g0217a0002c0003t0001g0218a0002c0003t0001g0219 | 3 | HG01257.hp2 HG01346.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.50-15923C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990651 | ||||||
| chr11:60990732
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0179 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.50-15842A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990732 | ||||||
| chr11:60990752
|
CAATG | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0006c0008t0001g0063 | 3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-15821_50-15818d others(6): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990752 | ||||||
| chr11:60990756
|
G | T | 1 | a0003c0005t0001g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.50-15818G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990756 | ||||||
| chr11:60990806
|
A | AGGCTGAG others(111): Show |
2 | a0002c0003t0001g0026a0009c0022t0001g0213 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.50-15768_50-15767i others(120): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990806 | ||||||
| chr11:60990806
|
A | AGGCTGAG others(111): Show |
15 | a0002c0003t0001g0030a0002c0003t0001g0059a0002c0003t0001g0066others(12): Show | 15 | HG00438.hp2 HG00639.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-15768_50-15767i others(120): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990806 | ||||||
| chr11:60990806
|
A | AGGCTGAG others(113): Show |
144 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(141): Show | 150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.50-15768_50-15767i others(122): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990806 | ||||||
| chr11:60990808
|
A | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(158): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.50-15766A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990808 | ||||||
| chr11:60990949
|
G | C | 1 | a0004c0004t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.50-15625G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990949 | ||||||
| chr11:60990989
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.50-15585G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990989 | ||||||
| chr11:60991139
|
C | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-15435C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991139 | ||||||
| chr11:60991141
|
T | C | 5 | a0001c0007t0001g0257a0002c0002t0001g0025a0002c0009t0001g0001others(2): Show | 7 | HG02257.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-15433T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991141 | ||||||
| chr11:60991148
|
TC | T | 4 | a0002c0002t0001g0025a0002c0009t0001g0001a0002c0009t0001g0023others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-15425delC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991148 | ||||||
| chr11:60991149
|
C | CT | 208 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(205): Show | 219 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.50-15407dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991149 | |||||
| chr11:60991149
|
C | CTT | 12 | a0001c0001t0001g0013a0002c0002t0001g0069a0002c0002t0001g0181others(9): Show | 13 | HG00323.hp2 HG00438.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.50-15408_50-15407d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991149 | |||||
| chr11:60991149
|
CT | C | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0203others(15): Show | 19 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.50-15407delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991149 | |||||
| chr11:60991152
|
T | TC | 4 | a0002c0003t0001g0002a0002c0003t0001g0021a0002c0003t0001g0022others(1): Show | 5 | HG01243.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-15422_50-15421i others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991152 | ||||||
| chr11:60991228
|
G | A | 4 | a0001c0007t0001g0252a0001c0007t0001g0266a0001c0007t0001g0267others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-15346G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991228 | ||||||
| chr11:60991297
|
T | G | 4 | a0001c0010t0002g0014a0001c0010t0002g0234a0001c0010t0002g0235others(1): Show | 5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-15277T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991297 | ||||||
| chr11:60991371
|
T | C | 2 | a0002c0002t0001g0239a0003c0011t0005g0047 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50-15203T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991371 | ||||||
| chr11:60991377
|
TC | T | 2 | a0001c0007t0001g0020a0003c0011t0004g0044 | 3 | HG02818.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.50-15194delC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991377 | |||||
| chr11:60991535
|
C | T | 1 | a0002c0003t0001g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-15039C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991535 | ||||||
| chr11:60991555
|
A | G | 11 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0007t0005g0275others(8): Show | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-15019A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991555 | ||||||
| chr11:60991571
|
T | C | 9 | a0001c0001t0007g0259a0001c0007t0001g0016a0001c0007t0001g0017others(6): Show | 10 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-15003T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991571 | ||||||
| chr11:60991648
|
C | CT | 7 | a0001c0001t0007g0040a0001c0010t0002g0014a0001c0010t0002g0234others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-14923dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991648 | |||||
| chr11:60991856
|
CTATATAT others(5): Show |
C | 11 | a0002c0003t0001g0030a0003c0005t0001g0027a0005c0006t0001g0028others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-14698_50-14687d others(14): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991856 | |||||
| chr11:60991873
|
T | G | 6 | a0002c0003t0001g0059a0002c0003t0001g0066a0002c0003t0001g0081others(3): Show | 6 | HG00438.hp2 HG02896.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-14701T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991873 | ||||||
| chr11:60991898
|
A | G | 2 | a0001c0007t0001g0020a0003c0011t0004g0044 | 3 | HG02818.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.50-14676A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991898 | ||||||
| chr11:60991922
|
G | T | 1 | a0002c0003t0001g0232 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.50-14652G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991922 | ||||||
| chr11:60991989
|
C | G | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-14585C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991989 | ||||||
| chr11:60992182
|
T | C | 19 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0007g0259others(16): Show | 21 | HG00140.hp1 HG01433.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.50-14392T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992182 | ||||||
| chr11:60992267
|
C | T | 7 | a0001c0010t0002g0133a0002c0002t0001g0037a0002c0002t0001g0038others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-14307C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992267 | ||||||
| chr11:60992332
|
C | CT | 96 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0048others(93): Show | 98 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.50-14231dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60992332 | |||||
| chr11:60992342
|
T | A | 1 | a0004c0004t0001g0273 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.50-14232T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992342 | ||||||
| chr11:60992375
|
G | A | 22 | a0001c0001t0001g0121a0001c0001t0001g0140a0001c0001t0001g0157others(19): Show | 22 | HG00438.hp2 HG00558.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.50-14199G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992375 | ||||||
| chr11:60992656
|
G | A | 1 | a0001c0001t0009g0176 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-13918G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992656 | ||||||
| chr11:60992705
|
G | A | 2 | a0005c0006t0001g0276a0005c0006t0001g0277 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.50-13869G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992705 | ||||||
| chr11:60992823
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.50-13751G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992823 | ||||||
| chr11:60992843
|
A | G | 1 | a0002c0002t0001g0156 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.50-13731A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992843 | ||||||
| chr11:60992887
|
C | T | 1 | a0002c0003t0001g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50-13687C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992887 | ||||||
| chr11:60992933
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-13641G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992933 | ||||||
| chr11:60993058
|
C | T | 95 | a0001c0001t0001g0202a0002c0002t0001g0010a0002c0002t0001g0025others(92): Show | 101 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.50-13516C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993058 | ||||||
| chr11:60993103
|
G | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0136others(4): Show | 7 | NA18946.hp2 NA18951.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-13471G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993103 | ||||||
| chr11:60993140
|
C | G | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-13434C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993140 | ||||||
| chr11:60993322
|
G | GAGAGAAT others(19): Show |
20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-13251_50-13250i others(28): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60993322 | |||||
| chr11:60993435
|
C | T | 6 | a0004c0004t0001g0018a0004c0004t0001g0120a0004c0004t0001g0167others(3): Show | 7 | HG00323.hp1 HG01123.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-13139C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993435 | ||||||
| chr11:60993480
|
C | A | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.50-13094C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993480 | ||||||
| chr11:60993499
|
G | A | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-13075G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993499 | ||||||
| chr11:60993507
|
C | A | 1 | a0001c0007t0001g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50-13067C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993507 | ||||||
| chr11:60993508
|
G | A | 5 | a0003c0005t0001g0230a0003c0011t0001g0227a0003c0011t0004g0044others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-13066G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993508 | ||||||
| chr11:60993525
|
C | T | 5 | a0003c0005t0001g0230a0003c0011t0001g0227a0003c0011t0004g0044others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-13049C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993525 | ||||||
| chr11:60993530
|
G | GT | 54 | a0001c0001t0001g0202a0002c0003t0001g0004a0003c0005t0001g0009others(51): Show | 59 | HG00323.hp1 HG00423.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.50-13043dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60993530 | |||||
| chr11:60993583
|
T | C | 1 | a0002c0016t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.50-12991T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993583 | ||||||
| chr11:60993606
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-12968C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993606 | ||||||
| chr11:60993645
|
G | A | 6 | a0007c0012t0001g0035a0007c0012t0003g0031a0007c0012t0003g0033others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-12929G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993645 | ||||||
| chr11:60993656
|
T | A | 1 | a0002c0003t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50-12918T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993656 | ||||||
| chr11:60993708
|
G | A | 1 | a0003c0005t0001g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.50-12866G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993708 | ||||||
| chr11:60993849
|
T | C | 19 | a0001c0001t0007g0259a0001c0007t0001g0016a0001c0007t0001g0017others(16): Show | 21 | HG02055.hp2 HG02257.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.50-12725T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993849 | ||||||
| chr11:60993904
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.50-12670G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993904 | ||||||
| chr11:60994033
|
C | T | 1 | a0002c0003t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.50-12541C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994033 | ||||||
| chr11:60994096
|
A | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.50-12478A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994096 | ||||||
| chr11:60994127
|
G | A | 1 | a0002c0003t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50-12447G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994127 | ||||||
| chr11:60994167
|
G | A | 2 | a0002c0002t0001g0197a0002c0002t0001g0198 | 2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.50-12407G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994167 | ||||||
| chr11:60994241
|
G | A | 5 | a0003c0005t0001g0230a0003c0011t0001g0227a0003c0011t0004g0044others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-12333G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994241 | ||||||
| chr11:60994272
|
C | T | 5 | a0003c0005t0001g0230a0003c0011t0001g0227a0003c0011t0004g0044others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-12302C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994272 | ||||||
| chr11:60994302
|
G | A | 1 | a0002c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.50-12272G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994302 | ||||||
| chr11:60994302
|
G | T | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-12272G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994302 | ||||||
| chr11:60994457
|
C | CAAAAAAA others(2): Show |
54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(51): Show | 57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.50-12111_50-12103d others(11): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0083others(17): Show | 20 | HG00423.hp1 HG01106.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.50-12112_50-12103d others(12): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(4): Show |
46 | a0001c0001t0001g0136a0001c0001t0007g0259a0001c0007t0001g0017others(43): Show | 52 | HG00741.hp2 HG01071.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.50-12113_50-12103d others(13): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(5): Show |
31 | a0001c0001t0011g0278a0001c0007t0001g0016a0001c0007t0001g0020others(28): Show | 33 | HG00099.hp2 HG00438.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.50-12114_50-12103d others(14): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(6): Show |
5 | a0002c0002t0001g0229a0002c0003t0001g0081a0002c0009t0001g0023others(2): Show | 5 | HG01081.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-12115_50-12103d others(15): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(7): Show |
42 | a0001c0001t0001g0062a0001c0001t0001g0203a0001c0001t0001g0208others(39): Show | 44 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.50-12116_50-12103d others(16): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(8): Show |
50 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0202others(47): Show | 53 | HG00323.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(17): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(9): Show |
8 | a0001c0001t0001g0153a0002c0002t0001g0069a0002c0002t0001g0072others(5): Show | 9 | HG01123.hp2 HG01175.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(18): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994457
|
C | CAAAAAAA others(10): Show |
2 | a0002c0002t0001g0070a0002c0002t0001g0071 | 2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.50-12103_50-12102i others(19): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | |||||
| chr11:60994465
|
A | AAAAAAAA others(8): Show |
6 | a0005c0006t0001g0086a0005c0006t0001g0089a0005c0006t0001g0114others(3): Show | 6 | HG01433.hp1 HG02074.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(17): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994465 | |||||
| chr11:60994465
|
A | AAAAAAAA others(7): Show |
14 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(11): Show | 16 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(16): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994465 | |||||
| chr11:60994509
|
G | A | 2 | a0002c0002t0001g0239a0003c0011t0005g0047 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50-12065G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994509 | ||||||
| chr11:60994511
|
A | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.50-12063A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994511 | ||||||
| chr11:60994562
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.50-12012T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994562 | ||||||
| chr11:60994584
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.50-11990C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994584 | ||||||
| chr11:60994777
|
C | A | 2 | a0002c0002t0001g0239a0003c0011t0005g0047 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50-11797C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994777 | ||||||
| chr11:60995026
|
G | A | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-11548G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995026 | ||||||
| chr11:60995102
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(74): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.50-11472C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995102 | ||||||
| chr11:60995125
|
CT | C | 73 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0011g0278others(70): Show | 81 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.50-11438delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60995125 | |||||
| chr11:60995128
|
T | C | 95 | a0001c0001t0001g0202a0002c0002t0001g0010a0002c0002t0001g0025others(92): Show | 101 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.50-11446T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995128 | ||||||
| chr11:60995156
|
C | T | 279 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(276): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.50-11418C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995156 | ||||||
| chr11:60995237
|
C | G | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-11337C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995237 | ||||||
| chr11:60995284
|
A | G | 49 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0011g0278others(46): Show | 55 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-11290A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995284 | ||||||
| chr11:60995378
|
C | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(72): Show | 78 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-11196C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995378 | ||||||
| chr11:60995426
|
T | A | 14 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(11): Show | 18 | HG01109.hp2 HG01243.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-11148T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995426 | ||||||
| chr11:60995662
|
C | A | 63 | a0002c0002t0001g0010a0002c0002t0001g0025a0002c0002t0001g0037others(60): Show | 67 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.50-10912C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995662 | ||||||
| chr11:60995724
|
A | ATCTTTTC others(19): Show |
1 | a0002c0003t0001g0103 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.50-10849_50-10824d others(28): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60995724 | |||||
| chr11:60995769
|
G | A | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-10805G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995769 | ||||||
| chr11:60996001
|
A | G | 1 | a0005c0006t0001g0200 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.50-10573A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996001 | ||||||
| chr11:60996134
|
T | C | 1 | a0001c0007t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.50-10440T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996134 | ||||||
| chr11:60996296
|
G | A | 14 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(11): Show | 18 | HG01109.hp2 HG01243.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-10278G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996296 | ||||||
| chr11:60996360
|
G | A | 77 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(74): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.50-10214G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996360 | ||||||
| chr11:60996549
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0097a0001c0001t0001g0104others(4): Show | 7 | HG00140.hp1 HG00323.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-10025C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996549 | ||||||
| chr11:60996556
|
A | G | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-10018A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996556 | ||||||
| chr11:60996589
|
C | T | 1 | a0003c0005t0001g0207 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.50-9985C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996589 | ||||||
| chr11:60997130
|
C | G | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-9444C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997130 | ||||||
| chr11:60997163
|
G | A | 1 | a0006c0008t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.50-9411G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997163 | ||||||
| chr11:60997192
|
G | A | 178 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0065others(175): Show | 192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-9382G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997192 | ||||||
| chr11:60997245
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.50-9329G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997245 | ||||||
| chr11:60997378
|
C | CA | 6 | a0001c0001t0001g0093a0001c0001t0001g0142a0001c0007t0001g0257others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-9182dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60997378 | |||||
| chr11:60997388
|
A | T | 34 | a0001c0001t0001g0202a0002c0003t0001g0004a0002c0003t0001g0030others(31): Show | 36 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.50-9186A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997388 | ||||||
| chr11:60997393
|
T | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(6): Show | 9 | HG02074.hp2 HG03098.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-9181T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997393 | ||||||
| chr11:60997523
|
A | T | 32 | a0001c0001t0001g0202a0002c0003t0001g0004a0003c0005t0001g0009others(29): Show | 34 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.50-9051A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997523 | ||||||
| chr11:60997700
|
G | T | 1 | a0001c0007t0001g0228 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-8874G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997700 | ||||||
| chr11:60997715
|
C | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.50-8859C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997715 | ||||||
| chr11:60997739
|
G | C | 1 | a0002c0002t0001g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.50-8835G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997739 | ||||||
| chr11:60997828
|
GA | G | 89 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0202others(86): Show | 97 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.50-8743delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60997828 | |||||
| chr11:60997883
|
G | A | 29 | a0002c0003t0001g0004a0003c0005t0001g0009a0003c0005t0001g0043others(26): Show | 31 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.50-8691G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997883 | ||||||
| chr11:60998041
|
G | A | 6 | a0004c0004t0001g0005a0004c0004t0001g0067a0004c0004t0001g0068others(3): Show | 7 | HG01168.hp2 HG02004.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-8533G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998041 | ||||||
| chr11:60998081
|
C | T | 89 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0202others(86): Show | 97 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.50-8493C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998081 | ||||||
| chr11:60998201
|
A | G | 1 | a0003c0005t0001g0253 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.50-8373A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998201 | ||||||
| chr11:60998512
|
A | G | 64 | a0002c0002t0001g0010a0002c0002t0001g0025a0002c0002t0001g0037others(61): Show | 68 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.50-8062A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998512 | ||||||
| chr11:60998606
|
G | C | 1 | a0006c0008t0001g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-7968G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998606 | ||||||
| chr11:60998607
|
C | G | 1 | a0006c0008t0001g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-7967C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998607 | ||||||
| chr11:60998614
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(2): Show | 5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-7960A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998614 | ||||||
| chr11:60998648
|
C | T | 49 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0011g0278others(46): Show | 55 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-7926C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998648 | ||||||
| chr11:60998680
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50-7894C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998680 | ||||||
| chr11:60998714
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.50-7860T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998714 | ||||||
| chr11:60998801
|
T | A | 1 | a0006c0008t0001g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-7773T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998801 | ||||||
| chr11:60998849
|
GA | G | 98 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(95): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.50-7706delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60998849 | |||||
| chr11:60998849
|
GAA | G | 108 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0150others(105): Show | 118 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.50-7707_50-7706del others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60998849 | |||||
| chr11:60998849
|
GAAA | G | 8 | a0002c0003t0001g0268a0006c0008t0001g0075a0007c0012t0001g0035others(5): Show | 8 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-7708_50-7706del others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60998849 | |||||
| chr11:60998934
|
G | A | 2 | a0003c0011t0004g0044a0003c0011t0004g0279 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50-7640G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998934 | ||||||
| chr11:60998965
|
C | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0170 | 2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.50-7609C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998965 | ||||||
| chr11:60999083
|
G | A | 97 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(94): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.50-7491G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999083 | ||||||
| chr11:60999090
|
G | A | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-7484G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999090 | ||||||
| chr11:60999273
|
T | C | 1 | a0003c0011t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-7301T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999273 | ||||||
| chr11:60999400
|
A | G | 6 | a0004c0004t0001g0018a0004c0004t0001g0120a0004c0004t0001g0167others(3): Show | 7 | HG00323.hp1 HG01123.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-7174A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999400 | ||||||
| chr11:60999469
|
C | A | 2 | a0002c0002t0001g0194a0002c0002t0014g0238 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.50-7105C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999469 | ||||||
| chr11:60999863
|
A | G | 34 | a0001c0001t0001g0202a0002c0003t0001g0004a0003c0005t0001g0009others(31): Show | 36 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.50-6711A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999863 | ||||||
| chr11:60999948
|
T | G | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-6626T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999948 | ||||||
| chr11:60999995
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.50-6579T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999995 | ||||||
| chr11:61000072
|
A | T | 1 | a0011c0015t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.50-6502A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000072 | ||||||
| chr11:61000222
|
A | G | 261 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.50-6352A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000222 | ||||||
| chr11:61000326
|
T | TA | 151 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0065others(148): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.50-6246dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61000326 | |||||
| chr11:61000351
|
A | G | 64 | a0002c0002t0001g0010a0002c0002t0001g0025a0002c0002t0001g0037others(61): Show | 68 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.50-6223A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000351 | ||||||
| chr11:61000492
|
C | T | 29 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(26): Show | 32 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-6082C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000492 | ||||||
| chr11:61000546
|
T | A | 29 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(26): Show | 32 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-6028T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000546 | ||||||
| chr11:61000565
|
C | G | 1 | a0003c0005t0001g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.50-6009C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000565 | ||||||
| chr11:61000572
|
G | A | 179 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(176): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.50-6002G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000572 | ||||||
| chr11:61001031
|
A | T | 11 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(8): Show | 11 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-5543A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001031 | ||||||
| chr11:61001198
|
C | CT | 106 | a0001c0001t0007g0259a0001c0001t0011g0278a0001c0007t0001g0016others(103): Show | 117 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.50-5356dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61001198 | |||||
| chr11:61001198
|
CT | C | 78 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(75): Show | 81 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.50-5356delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61001198 | |||||
| chr11:61001240
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.50-5334G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001240 | ||||||
| chr11:61001254
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0004c0004t0001g0210 | 3 | HG01884.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.50-5320G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001254 | ||||||
| chr11:61001264
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0152a0007c0012t0001g0035others(3): Show | 7 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-5310C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001264 | ||||||
| chr11:61001373
|
T | A | 6 | a0007c0012t0001g0035a0007c0012t0003g0031a0007c0012t0003g0033others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-5201T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001373 | ||||||
| chr11:61001481
|
G | A | 140 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(137): Show | 147 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.50-5093G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001481 | ||||||
| chr11:61001597
|
C | CT | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-4974dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61001597 | |||||
| chr11:61002062
|
T | C | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-4512T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002062 | ||||||
| chr11:61002245
|
A | T | 39 | a0001c0001t0001g0202a0002c0003t0001g0004a0003c0005t0001g0009others(36): Show | 41 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.50-4329A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002245 | ||||||
| chr11:61002347
|
G | A | 43 | a0001c0001t0011g0278a0002c0003t0001g0002a0002c0003t0001g0007others(40): Show | 48 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.50-4227G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002347 | ||||||
| chr11:61002540
|
G | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-4034G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002540 | ||||||
| chr11:61002720
|
T | C | 261 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.50-3854T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002720 | ||||||
| chr11:61002954
|
C | CTCTTT | 59 | a0001c0001t0007g0040a0002c0002t0001g0010a0002c0002t0001g0025others(56): Show | 63 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.50-3598_50-3594dup others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | |||||
| chr11:61002954
|
C | CTCTTTTC others(3): Show |
73 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(70): Show | 76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.50-3603_50-3594dup others(10): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | |||||
| chr11:61002954
|
C | CTCTTTTC others(8): Show |
7 | a0001c0001t0001g0058a0001c0001t0001g0095a0001c0001t0001g0125others(4): Show | 7 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-3608_50-3594dup others(15): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | |||||
| chr11:61002954
|
CTCTTT | C | 44 | a0001c0001t0011g0278a0002c0002t0001g0091a0002c0003t0001g0002others(41): Show | 49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.50-3598_50-3594del others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | |||||
| chr11:61002977
|
T | TTTTCTTT others(3): Show |
1 | a0008c0013t0001g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.50-3594_50-3593ins others(10): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002977 | |||||
| chr11:61003069
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50-3505A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003069 | ||||||
| chr11:61003089
|
G | A | 1 | a0002c0003t0001g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-3485G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003089 | ||||||
| chr11:61003129
|
T | C | 187 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(184): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.50-3445T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003129 | ||||||
| chr11:61003194
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.50-3380A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003194 | ||||||
| chr11:61003211
|
C | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.50-3363C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003211 | ||||||
| chr11:61003261
|
A | G | 64 | a0002c0002t0001g0010a0002c0002t0001g0025a0002c0002t0001g0037others(61): Show | 68 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.50-3313A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003261 | ||||||
| chr11:61003605
|
G | A | 24 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(21): Show | 27 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-2969G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003605 | ||||||
| chr11:61003648
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-2926C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003648 | ||||||
| chr11:61003649
|
G | A | 1 | a0003c0005t0001g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.50-2925G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003649 | ||||||
| chr11:61003683
|
G | A | 2 | a0003c0005t0001g0163a0003c0005t0001g0172 | 2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.50-2891G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003683 | ||||||
| chr11:61003713
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0004c0004t0001g0210 | 3 | HG01884.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.50-2861G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003713 | ||||||
| chr11:61003877
|
G | T | 2 | a0002c0002t0001g0132a0002c0002t0001g0241 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.50-2697G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003877 | ||||||
| chr11:61003898
|
G | A | 22 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(19): Show | 25 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-2676G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003898 | ||||||
| chr11:61003919
|
AAAAT | A | 38 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(35): Show | 39 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.50-2651_50-2648del others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61003919 | |||||
| chr11:61003951
|
C | A | 4 | a0002c0003t0001g0231a0002c0003t0001g0232a0002c0003t0001g0233others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-2623C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003951 | ||||||
| chr11:61003978
|
G | GCTCA | 280 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(277): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.50-2595_50-2592dup others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61003978 | |||||
| chr11:61004226
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0152 | 3 | NA18948.hp2 NA18986.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.50-2348A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004226 | ||||||
| chr11:61004278
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(2): Show | 5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-2296A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004278 | ||||||
| chr11:61004455
|
G | A | 29 | a0003c0005t0001g0009a0003c0005t0001g0027a0003c0005t0001g0043others(26): Show | 30 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.50-2119G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004455 | ||||||
| chr11:61004473
|
C | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.50-2101C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004473 | ||||||
| chr11:61004508
|
G | A | 22 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(19): Show | 25 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-2066G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004508 | ||||||
| chr11:61004525
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-2049T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004525 | ||||||
| chr11:61004618
|
C | T | 190 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(187): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.50-1956C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004618 | ||||||
| chr11:61004619
|
G | A | 1 | a0003c0011t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-1955G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004619 | ||||||
| chr11:61004735
|
C | G | 4 | a0003c0011t0001g0227a0003c0011t0004g0044a0003c0011t0004g0045others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1839C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004735 | ||||||
| chr11:61004796
|
C | G | 43 | a0002c0003t0001g0002a0002c0003t0001g0004a0002c0003t0001g0007others(40): Show | 49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.50-1778C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004796 | ||||||
| chr11:61004849
|
A | G | 1 | a0001c0007t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.50-1725A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004849 | ||||||
| chr11:61004909
|
G | A | 24 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(21): Show | 27 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-1665G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004909 | ||||||
| chr11:61005067
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-1507C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005067 | ||||||
| chr11:61005128
|
C | A | 1 | a0001c0001t0009g0176 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-1446C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005128 | ||||||
| chr11:61005220
|
A | G | 1 | a0005c0006t0001g0032 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.50-1354A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005220 | ||||||
| chr11:61005267
|
G | T | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-1307G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005267 | ||||||
| chr11:61005370
|
C | T | 1 | a0002c0003t0001g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.50-1204C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005370 | ||||||
| chr11:61005388
|
C | T | 22 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(19): Show | 25 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-1186C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005388 | ||||||
| chr11:61005394
|
C | T | 6 | a0006c0008t0001g0074a0006c0008t0001g0075a0006c0008t0001g0119others(3): Show | 6 | HG00673.hp1 HG02080.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-1180C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005394 | ||||||
| chr11:61005449
|
A | C | 34 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(31): Show | 35 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-1125A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005449 | ||||||
| chr11:61005595
|
G | A | 3 | a0002c0003t0001g0004a0002c0003t0001g0103a0002c0003t0001g0169 | 4 | HG01069.hp1 HG01071.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-979G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005595 | ||||||
| chr11:61005653
|
T | C | 248 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.50-921T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005653 | ||||||
| chr11:61005659
|
T | C | 263 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(260): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.50-915T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005659 | ||||||
| chr11:61005729
|
C | T | 1 | a0001c0018t0001g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.50-845C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005729 | ||||||
| chr11:61005792
|
G | A | 1 | a0002c0003t0001g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-782G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005792 | ||||||
| chr11:61005855
|
T | C | 248 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.50-719T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005855 | ||||||
| chr11:61005867
|
G | A | 2 | a0002c0002t0001g0010a0002c0002t0001g0212 | 3 | HG02280.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.50-707G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005867 | ||||||
| chr11:61005880
|
G | A | 63 | a0002c0003t0001g0002a0002c0003t0001g0004a0002c0003t0001g0007others(60): Show | 71 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.50-694G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005880 | ||||||
| chr11:61005931
|
C | CA | 90 | a0001c0001t0007g0040a0001c0001t0007g0259a0002c0003t0001g0002others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.50-630dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61005931 | |||||
| chr11:61005941
|
A | AG | 34 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(31): Show | 35 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-633_50-632insG | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005941 | ||||||
| chr11:61005941
|
A | G | 32 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0080others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-633A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005941 | ||||||
| chr11:61006232
|
A | T | 6 | a0007c0012t0001g0035a0007c0012t0003g0031a0007c0012t0003g0033others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-342A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61006232 | ||||||
| chr11:61006417
|
G | A | 1 | a0006c0008t0001g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.50-157G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61006417 | ||||||
| chr11:61006462
|
G | T | 1 | a0001c0010t0002g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.50-112G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61006462 | ||||||
| chr11:61006838
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.118+196A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61006838 | ||||||
| chr11:61006904
|
G | A | 8 | a0002c0003t0001g0004a0002c0003t0001g0059a0002c0003t0001g0066others(5): Show | 9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.118+262G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61006904 | ||||||
| chr11:61006952
|
C | T | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+310C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61006952 | ||||||
| chr11:61007106
|
G | C | 59 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(56): Show | 62 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.119-454G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007106 | ||||||
| chr11:61007184
|
A | G | 59 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(56): Show | 62 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.119-376A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007184 | ||||||
| chr11:61007287
|
T | C | 5 | a0003c0005t0001g0230a0003c0011t0001g0227a0003c0011t0004g0044others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-273T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007287 | ||||||
| chr11:61007381
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(2): Show | 5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-179G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007381 | ||||||
| chr11:61007480
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.119-80C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007480 | ||||||
| chr11:61007535
|
C | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(77): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.119-25C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007535 | ||||||
| chr11:61007920
|
C | T | 1 | a0001c0007t0005g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.469+10C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/12 | chr11 | 61007920 | ||||||
| chr11:61007957
|
G | A | 1 | a0007c0012t0010g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.469+47G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/12 | chr11 | 61007957 | ||||||
| chr11:61008155
|
G | T | 24 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(21): Show | 27 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.469+245G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/12 | chr11 | 61008155 | ||||||
| chr11:61008861
|
C | T | 22 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(19): Show | 25 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.781+16C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61008861 | ||||||
| chr11:61008862
|
A | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.781+17A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61008862 | ||||||
| chr11:61008993
|
A | G | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.781+148A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61008993 | ||||||
| chr11:61009012
|
T | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(73): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.781+167T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009012 | ||||||
| chr11:61009182
|
G | A | 4 | a0002c0003t0001g0231a0002c0003t0001g0232a0002c0003t0001g0233others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+337G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009182 | ||||||
| chr11:61009239
|
A | G | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.782-333A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009239 | ||||||
| chr11:61009309
|
T | C | 111 | a0001c0007t0001g0257a0002c0002t0001g0010a0002c0002t0001g0025others(108): Show | 121 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.782-263T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009309 | ||||||
| chr11:61009334
|
G | A | 24 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(21): Show | 27 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.782-238G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009334 | ||||||
| chr11:61009361
|
G | A | 2 | a0006c0008t0001g0063a0006c0008t0001g0139 | 2 | HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.782-211G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009361 | ||||||
| chr11:61009361
|
G | C | 1 | a0001c0001t0001g0261 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.782-211G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009361 | ||||||
| chr11:61009977
|
CA | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(2): Show | 5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+105delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 61009977 | |||||
| chr11:61010084
|
A | T | 34 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(31): Show | 35 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1084+210A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010084 | ||||||
| chr11:61010236
|
AC | A | 5 | a0003c0005t0001g0230a0003c0011t0001g0227a0003c0011t0004g0044others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084+365delC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 61010236 | |||||
| chr11:61010307
|
A | G | 1 | a0002c0009t0001g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1084+433A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010307 | ||||||
| chr11:61010442
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0153 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1084+568C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010442 | ||||||
| chr11:61010502
|
A | G | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085-568A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010502 | ||||||
| chr11:61010519
|
A | C | 1 | a0002c0002t0001g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1085-551A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010519 | ||||||
| chr11:61010565
|
A | C | 1 | a0008c0013t0001g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1085-505A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010565 | ||||||
| chr11:61010788
|
C | T | 2 | a0002c0003t0001g0030a0002c0003t0001g0216 | 2 | HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1085-282C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010788 | ||||||
| chr11:61010793
|
T | C | 6 | a0007c0012t0001g0035a0007c0012t0003g0031a0007c0012t0003g0033others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085-277T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010793 | ||||||
| chr11:61010856
|
A | T | 1 | a0001c0001t0011g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1085-214A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010856 | ||||||
| chr11:61010977
|
C | T | 5 | a0001c0007t0001g0257a0002c0003t0001g0039a0002c0003t0001g0221others(2): Show | 5 | HG01261.hp1 HG01496.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085-93C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010977 | ||||||
| chr11:61011041
|
T | C | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1085-29T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61011041 | ||||||
| chr11:61011055
|
G | A | 1 | a0003c0011t0004g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1085-15G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61011055 | ||||||
| chr11:61011158
|
C | T | 2 | a0002c0003t0001g0242a0002c0003t0001g0246 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1150+23C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011158 | ||||||
| chr11:61011178
|
C | CGGTGTGT others(8): Show |
1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1150+44_1150+45ins others(15): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGT | 17 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(14): Show | 19 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.1150+68_1150+69dup others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGT | 36 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0065others(33): Show | 39 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+66_1150+69dup others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGT | 3 | a0002c0003t0001g0242a0002c0003t0001g0246a0005c0006t0001g0247 | 3 | HG00741.hp2 HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1150+64_1150+69dup others(6): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(1): Show |
11 | a0001c0007t0001g0257a0002c0003t0001g0026a0002c0003t0001g0039others(8): Show | 11 | HG01261.hp1 HG01496.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1150+62_1150+69dup others(8): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(3): Show |
40 | a0001c0001t0001g0079a0001c0001t0009g0176a0002c0002t0001g0037others(37): Show | 44 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1150+60_1150+69dup others(10): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(5): Show |
9 | a0001c0001t0001g0154a0001c0001t0001g0261a0001c0001t0011g0278others(6): Show | 12 | HG01884.hp1 HG02280.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150+58_1150+69dup others(12): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(7): Show |
89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(86): Show | 93 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1150+56_1150+69dup others(14): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(9): Show |
27 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0178others(24): Show | 27 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1150+54_1150+69dup others(16): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(11): Show |
20 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0125others(17): Show | 20 | HG00438.hp1 HG01516.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1150+52_1150+69dup others(18): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011178
|
C | CGTGTGTG others(13): Show |
2 | a0002c0002t0001g0262a0003c0005t0001g0085 | 2 | HG00408.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1150+50_1150+69dup others(20): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | |||||
| chr11:61011232
|
G | C | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+97G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011232 | ||||||
| chr11:61011242
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1150+107G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011242 | ||||||
| chr11:61011246
|
T | C | 43 | a0002c0002t0001g0010a0002c0002t0001g0025a0002c0002t0001g0037others(40): Show | 44 | HG00438.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1150+111T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011246 | ||||||
| chr11:61011411
|
CA | C | 21 | a0002c0003t0001g0004a0002c0003t0001g0007a0002c0003t0001g0011others(18): Show | 24 | HG00099.hp2 HG00438.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1150+277delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011411 | ||||||
| chr11:61011438
|
T | C | 1 | a0004c0004t0001g0210 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1150+303T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011438 | ||||||
| chr11:61011438
|
T | TA | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1150+304dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011438 | |||||
| chr11:61011490
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0153 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1150+355G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011490 | ||||||
| chr11:61011514
|
A | G | 164 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(161): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1150+379A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011514 | ||||||
| chr11:61011636
|
C | CAAGAAAG others(359): Show |
1 | a0003c0005t0001g0165 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1150+514_1150+515i others(368): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011636 | |||||
| chr11:61011886
|
T | C | 26 | a0001c0001t0001g0064a0001c0001t0001g0065a0004c0004t0001g0005others(23): Show | 29 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1150+751T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011886 | ||||||
| chr11:61011975
|
T | A | 1 | a0003c0005t0001g0172 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1150+840T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011975 | ||||||
| chr11:61011977
|
C | T | 2 | a0005c0006t0001g0118a0005c0006t0001g0193 | 2 | HG01255.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1150+842C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011977 | ||||||
| chr11:61012268
|
G | A | 36 | a0002c0002t0001g0010a0002c0002t0001g0025a0002c0002t0001g0037others(33): Show | 37 | HG00438.hp1 HG00735.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1150+1133G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012268 | ||||||
| chr11:61012290
|
T | A | 4 | a0003c0011t0001g0227a0003c0011t0004g0044a0003c0011t0004g0045others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-1133T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012290 | ||||||
| chr11:61012330
|
T | C | 42 | a0001c0007t0001g0257a0002c0003t0001g0002a0002c0003t0001g0004others(39): Show | 48 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1151-1093T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012330 | ||||||
| chr11:61012351
|
G | A | 25 | a0001c0001t0001g0064a0001c0001t0001g0065a0004c0004t0001g0005others(22): Show | 28 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1151-1072G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012351 | ||||||
| chr11:61012356
|
C | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(161): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1151-1067C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012356 | ||||||
| chr11:61012535
|
G | A | 20 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(17): Show | 22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1151-888G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012535 | ||||||
| chr11:61012565
|
C | G | 3 | a0002c0003t0001g0039a0002c0003t0001g0221a0002c0003t0001g0222 | 3 | HG01261.hp1 HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1151-858C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012565 | ||||||
| chr11:61012829
|
G | A | 27 | a0001c0001t0001g0202a0001c0007t0005g0275a0003c0005t0001g0009others(24): Show | 28 | HG00408.hp1 HG00423.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.1151-594G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012829 | ||||||
| chr11:61012830
|
G | A | 1 | a0006c0008t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1151-593G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012830 | ||||||
| chr11:61013385
|
A | G | 5 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0082others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-38A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61013385 | ||||||
| chr11:61013622
|
C | T | 36 | a0001c0001t0001g0202a0003c0005t0001g0009a0003c0005t0001g0027others(33): Show | 37 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1291+59C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013622 | ||||||
| chr11:61013638
|
G | A | 21 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(18): Show | 23 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1291+75G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013638 | ||||||
| chr11:61013651
|
G | A | 21 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(18): Show | 23 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1291+88G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013651 | ||||||
| chr11:61013790
|
G | A | 2 | a0001c0001t0001g0146a0003c0011t0001g0227 | 2 | HG00673.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1292-129G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013790 | ||||||
| chr11:61013791
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0203others(2): Show | 5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-128C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013791 | ||||||
| chr11:61013793
|
C | T | 4 | a0001c0001t0007g0040a0001c0001t0007g0259a0002c0002t0001g0132others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-126C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013793 | ||||||
| chr11:61014734
|
C | CA | 9 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG01884.hp2 HG02572.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387+735dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 61014734 | |||||
| chr11:61014734
|
CA | C | 16 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0095others(13): Show | 16 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.1387+735delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 61014734 | |||||
| chr11:61014741
|
A | AC | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387+727_1387+728i others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61014741 | ||||||
| chr11:61014757
|
T | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1387+743T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61014757 | ||||||
| chr11:61014857
|
G | C | 42 | a0001c0007t0001g0257a0002c0003t0001g0002a0002c0003t0001g0004others(39): Show | 48 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1387+843G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61014857 | ||||||
| chr11:61015126
|
G | A | 2 | a0004c0004t0001g0270a0004c0004t0001g0272 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1388-587G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015126 | ||||||
| chr11:61015130
|
TA | T | 6 | a0007c0012t0001g0035a0007c0012t0003g0031a0007c0012t0003g0033others(3): Show | 6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1388-580delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 61015130 | |||||
| chr11:61015162
|
G | A | 22 | a0004c0004t0001g0005a0004c0004t0001g0015a0004c0004t0001g0018others(19): Show | 25 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1388-551G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015162 | ||||||
| chr11:61015194
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1388-519G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015194 | ||||||
| chr11:61015213
|
A | G | 1 | a0001c0007t0005g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1388-500A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015213 | ||||||
| chr11:61015315
|
A | G | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388-398A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015315 | ||||||
| chr11:61015351
|
G | A | 4 | a0001c0010t0002g0014a0001c0010t0002g0133a0001c0010t0002g0234others(1): Show | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388-362G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015351 | ||||||
| chr11:61015373
|
A | C | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1388-340A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015373 | ||||||
| chr11:61015401
|
T | C | 1 | a0002c0003t0001g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1388-312T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015401 | ||||||
| chr11:61015464
|
G | A | 1 | a0002c0003t0001g0066 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1388-249G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015464 | ||||||
| chr11:61015590
|
A | G | 4 | a0005c0006t0001g0012a0005c0006t0001g0200a0005c0006t0001g0244others(1): Show | 5 | HG01099.hp2 HG01123.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388-123A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015590 | ||||||
| chr11:61015596
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1388-117C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015596 | ||||||
| chr11:61015636
|
C | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(171): Show | 182 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1388-77C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015636 | ||||||
| chr11:61015654
|
C | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1388-59C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015654 | ||||||
| chr11:61015663
|
A | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(278): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1388-50A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015663 | ||||||
| chr11:61016013
|
G | A | 1 | a0003c0005t0001g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1510+178G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016013 | ||||||
| chr11:61016013
|
G | T | 1 | a0001c0001t0011g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1510+178G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016013 | ||||||
| chr11:61016147
|
G | T | 1 | a0002c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1510+312G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016147 | ||||||
| chr11:61016159
|
G | A | 23 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(20): Show | 25 | HG02145.hp2 HG02572.hp1 HG02818.hp1 others(22): Show |
intron_variant | MODIFIER | c.1510+324G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016159 | ||||||
| chr11:61016188
|
C | T | 1 | a0003c0011t0005g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1510+353C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016188 | ||||||
| chr11:61016205
|
C | T | 2 | a0005c0006t0001g0276a0005c0006t0001g0277 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1510+370C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016205 | ||||||
| chr11:61016206
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1510+371G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016206 | ||||||
| chr11:61016261
|
C | T | 5 | a0007c0012t0001g0035a0007c0012t0003g0031a0007c0012t0003g0033others(2): Show | 5 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510+426C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016261 | ||||||
| chr11:61016332
|
C | T | 31 | a0005c0006t0001g0008a0005c0006t0001g0012a0005c0006t0001g0028others(28): Show | 33 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1510+497C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016332 | ||||||
| chr11:61016487
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1510+652A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016487 | ||||||
| chr11:61016510
|
T | C | 1 | a0003c0005t0001g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1510+675T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016510 | ||||||
| chr11:61016637
|
C | T | 3 | a0003c0005t0001g0160a0003c0005t0001g0164a0003c0005t0001g0185 | 3 | HG02165.hp2 NA18747.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1510+802C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016637 | ||||||
| chr11:61016638
|
G | A | 1 | a0003c0011t0005g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1510+803G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016638 | ||||||
| chr11:61016679
|
C | T | 1 | a0002c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1511-800C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016679 | ||||||
| chr11:61016803
|
G | A | 118 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1511-676G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016803 | ||||||
| chr11:61016814
|
C | T | 21 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(18): Show | 23 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1511-665C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016814 | ||||||
| chr11:61016848
|
C | T | 1 | a0004c0004t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1511-631C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016848 | ||||||
| chr11:61016854
|
CT | C | 2 | a0004c0004t0001g0015a0004c0004t0001g0237 | 3 | HG01069.hp2 HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1511-624delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016854 | ||||||
| chr11:61016906
|
C | A | 1 | a0003c0005t0001g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1511-573C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016906 | ||||||
| chr11:61016929
|
T | A | 1 | a0001c0007t0005g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1511-550T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016929 | ||||||
| chr11:61017151
|
CCTT | C | 32 | a0002c0009t0001g0001a0002c0009t0001g0023a0002c0009t0001g0024others(29): Show | 37 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1511-325_1511-323d others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 61017151 | |||||
| chr11:61017396
|
C | T | 2 | a0001c0001t0007g0040a0001c0001t0007g0259 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1511-83C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61017396 | ||||||
| chr11:61017462
|
A | G | 129 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(126): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1511-17A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61017462 | ||||||
| chr11:61017464
|
C | T | 1 | a0003c0005t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1511-15C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61017464 | ||||||
| chr11:61017566
|
A | G | 129 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(126): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1582+16A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 10/12 | chr11 | 61017566 | ||||||
| chr11:61018143
|
G | A | 1 | a0001c0007t0005g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1837+130G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/12 | chr11 | 61018143 | ||||||
| chr11:61018178
|
A | G | 1 | a0002c0002t0001g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1838-111A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/12 | chr11 | 61018178 | ||||||
| chr11:61018251
|
T | C | 60 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(57): Show | 66 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1838-38T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/12 | chr11 | 61018251 | ||||||
| chr11:61018480
|
C | CAAGGGGA others(12): Show |
60 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(57): Show | 66 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1942+93_1942+111du others(20): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr11 | 61018480 | |||||
| chr11:61018635
|
T | C | 1 | a0004c0004t0001g0273 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1942+242T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018635 | ||||||
| chr11:61018677
|
C | T | 1 | a0005c0006t0001g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1942+284C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018677 | ||||||
| chr11:61018681
|
G | GGTA | 98 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(95): Show | 110 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1942+290_1942+292d others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr11 | 61018681 | |||||
| chr11:61018740
|
C | A | 5 | a0001c0007t0002g0258a0001c0010t0002g0014a0001c0010t0002g0133others(2): Show | 6 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1942+347C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018740 | ||||||
| chr11:61018771
|
T | G | 9 | a0002c0003t0001g0004a0002c0003t0001g0059a0002c0003t0001g0066others(6): Show | 10 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1942+378T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018771 | ||||||
| chr11:61018817
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0151a0001c0001t0001g0154 | 3 | HG01943.hp2 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1942+424C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018817 | ||||||
| chr11:61019002
|
T | C | 98 | a0001c0007t0001g0016a0001c0007t0001g0017a0001c0007t0001g0020others(95): Show | 110 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1943-252T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61019002 | ||||||
| chr11:61019002
|
T | G | 1 | a0002c0003t0001g0124 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1943-252T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61019002 | ||||||
| chr11:61019072
|
C | T | 1 | a0001c0018t0001g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1943-182C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61019072 |