Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 920 |
|---|---|
| ensemblid | ENSG00000010610.10 |
| hgncid | 1678 |
| symbol | CD4 |
| name | CD4 molecule |
| refseq_nuc | NM_000616.5 |
| refseq_prot | NP_000607.1 |
| ensembl_nuc | ENST00000011653.9 |
| ensembl_prot | ENSP00000011653.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 6789528 |
| end | 6820799 |
| strand | + |
| ver | v1.2 |
| region | chr12:6789528-6820799 |
| region5000 | chr12:6784528-6825799 |
| regionname0 | CD4_chr12_6789528_6820799 |
| regionname5000 | CD4_chr12_6784528_6825799 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 458 | 383 | 66 | 67 | 190 | 16 | 42 | 145 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002 | 0/0 | 458 | 40 | 24 | 2 | 13 | 0 | 1 | 13 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0003 | 0/0 | 458 | 7 | 4 | 3 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0004 | 0/0 | 458 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0005 | 0/0 | 458 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0006 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0007 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0008 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0009 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0010 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0011 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0012 | 0/0 | 458 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1377 | 290 | 45 | 43 | 170 | 7 | 24 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0002 | 1/0 | 1377 | 78 | 15 | 23 | 15 | 9 | 15 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0003 | 0/0 | 1377 | 38 | 22 | 2 | 13 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0004 | 0/0 | 1377 | 7 | 0 | 0 | 4 | 0 | 3 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0005 | 0/0 | 1377 | 5 | 3 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0006 | 0/0 | 1377 | 4 | 3 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0007 | 0/0 | 1377 | 3 | 0 | 0 | 3 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0008 | 0/0 | 1377 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0009 | 0/0 | 1377 | 2 | 1 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0010 | 0/0 | 1377 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0011 | 0/0 | 1377 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0012 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0013 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0014 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0015 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0016 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0017 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0018 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0019 | 0/0 | 1377 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| c0020 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1673 | 140 | 28 | 17 | 84 | 1 | 10 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0002 | 0/1 | 1673 | 122 | 11 | 26 | 70 | 6 | 8 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0003 | 0/0 | 1673 | 79 | 19 | 21 | 15 | 9 | 15 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0004 | 0/0 | 1673 | 68 | 26 | 4 | 30 | 0 | 8 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0005 | 0/0 | 1675 | 7 | 7 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0006 | 0/0 | 1673 | 7 | 0 | 0 | 4 | 0 | 3 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0007 | 0/0 | 1673 | 4 | 2 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0008 | 0/0 | 1673 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0009 | 0/0 | 1673 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0010 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0011 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0012 | 0/0 | 1681 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0013 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0014 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0015 | 0/0 | 1673 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0016 | 0/0 | 1673 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0017 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0018 | 0/0 | 1673 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0019 | 0/0 | 1673 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| t0020 | 1/0 | 1673 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0406 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0407 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0414 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0417 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0419 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0420 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0421 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0422 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0423 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0424 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0425 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0426 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0427 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0428 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0429 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0430 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0431 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0432 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0433 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0434 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| g0435 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1377 | 290 | 45 | 43 | 170 | 7 | 24 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0002 | 1/0 | 1377 | 78 | 15 | 23 | 15 | 9 | 15 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0004 | 0/0 | 1377 | 7 | 0 | 0 | 4 | 0 | 3 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0006 | 0/0 | 1377 | 4 | 3 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0010 | 0/0 | 1377 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0012 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0018 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0003 | 0/0 | 1377 | 38 | 22 | 2 | 13 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0011 | 0/0 | 1377 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0003c0005 | 0/0 | 1377 | 5 | 3 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0003c0009 | 0/0 | 1377 | 2 | 1 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0004c0007 | 0/0 | 1377 | 3 | 0 | 0 | 3 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0005c0008 | 0/0 | 1377 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0006c0013 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0007c0020 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0008c0014 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0009c0016 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0010c0015 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0011c0017 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0012c0019 | 0/0 | 1377 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3049 | 128 | 17 | 16 | 84 | 1 | 10 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0002 | 0/1 | 3049 | 98 | 2 | 26 | 56 | 6 | 7 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0003 | 0/0 | 3049 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0004 | 0/0 | 3049 | 54 | 21 | 1 | 25 | 0 | 7 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0009 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0010 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0011 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0012 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0013 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0014 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0015 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0001t0017 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0002t0003 | 0/0 | 3049 | 75 | 15 | 21 | 15 | 9 | 15 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0002t0008 | 0/0 | 3049 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0002t0020 | 1/0 | 3049 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0004t0006 | 0/0 | 3049 | 7 | 0 | 0 | 4 | 0 | 3 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0006t0001 | 0/0 | 3049 | 4 | 3 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0010t0003 | 0/0 | 3049 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0012t0002 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0001c0018t0002 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0003t0001 | 0/0 | 3049 | 5 | 5 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0003t0002 | 0/0 | 3049 | 22 | 8 | 0 | 13 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0003t0005 | 0/0 | 3051 | 6 | 6 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0003t0007 | 0/0 | 3049 | 4 | 2 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0003t0018 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0011t0001 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0002c0011t0005 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0003c0005t0004 | 0/0 | 3049 | 5 | 3 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0003c0009t0004 | 0/0 | 3049 | 2 | 1 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0004c0007t0004 | 0/0 | 3049 | 3 | 0 | 0 | 3 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0005c0008t0004 | 0/0 | 3049 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0006c0013t0009 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0007c0020t0004 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0008c0014t0016 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0009c0016t0001 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0010c0015t0019 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0011c0017t0001 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| a0012c0019t0004 | 0/0 | 3049 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | copy fasta | chr12 | 6784528 | 6825799 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0407 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0406 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0425 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0426 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0013g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0017g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0430 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0008g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0008g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0020g0414 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0010t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0010t0003g0422 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0012t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0018t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0420 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0429 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0421 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0424 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0417 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0427 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0011t0001g0419 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0011t0005g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0431 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0432 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0433 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0434 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0435 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0009t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0009t0004g0428 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0004c0007t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0004c0007t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0004c0007t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0005c0008t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0006c0013t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0007c0020t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0008c0014t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0009c0016t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0010c0015t0019g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0011c0017t0001g0423 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0012c0019t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0346 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0131 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0289 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0407 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0058 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0213 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00408 | hp1 | a0001 | c0004 | t0006 | g0393 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0409 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00597 | hp1 | a0001 | c0004 | t0006 | g0074 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00609 | hp1 | a0001 | c0004 | t0006 | g0230 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00639 | hp2 | a0001 | c0006 | t0001 | g0338 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0350 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0347 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0329 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00738 | hp1 | a0003 | c0009 | t0004 | g0428 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0114 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01069 | hp1 | a0001 | c0002 | t0008 | g0275 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0340 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01071 | hp2 | a0001 | c0002 | t0008 | g0273 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0234 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0199 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0231 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0339 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0415 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0278 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01167 | hp2 | a0003 | c0005 | t0004 | g0435 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01169 | hp2 | a0003 | c0005 | t0004 | g0434 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0193 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0128 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0385 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0239 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0055 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01358 | hp1 | a0002 | c0003 | t0007 | g0427 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0287 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0198 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0202 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0238 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0197 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0137 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0052 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01884 | hp2 | a0002 | c0003 | t0002 | g0424 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01891 | hp1 | a0010 | c0015 | t0019 | g0255 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0327 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0400 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0389 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01993 | hp2 | a0002 | c0003 | t0007 | g0027 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0388 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0367 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0392 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02055 | hp1 | a0002 | c0003 | t0002 | g0421 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02071 | hp1 | a0004 | c0007 | t0004 | g0209 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02074 | hp1 | a0004 | c0007 | t0004 | g0208 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0403 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02135 | hp2 | a0004 | c0007 | t0004 | g0227 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02145 | hp1 | a0008 | c0014 | t0016 | g0264 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02145 | hp2 | a0002 | c0003 | t0007 | g0417 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0334 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0386 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0247 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0290 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0258 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02615 | hp1 | a0002 | c0003 | t0005 | g0303 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02615 | hp2 | a0003 | c0005 | t0004 | g0431 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02622 | hp1 | a0002 | c0003 | t0018 | g0016 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0032 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02630 | hp1 | a0001 | c0010 | t0003 | g0422 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0425 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02647 | hp2 | a0009 | c0016 | t0001 | g0031 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0150 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02717 | hp1 | a0011 | c0017 | t0001 | g0423 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0132 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0143 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0194 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0405 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0054 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0272 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02809 | hp2 | a0003 | c0005 | t0004 | g0433 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02818 | hp2 | a0002 | c0003 | t0002 | g0270 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0306 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02895 | hp2 | a0002 | c0003 | t0007 | g0267 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02896 | hp2 | a0002 | c0003 | t0005 | g0029 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02897 | hp2 | a0002 | c0003 | t0005 | g0030 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0279 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0349 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0336 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0026 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0295 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0167 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03139 | hp2 | a0007 | c0020 | t0004 | g0322 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03195 | hp1 | a0001 | c0010 | t0003 | g0257 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0280 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0291 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0294 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0037 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0008 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03486 | hp1 | a0002 | c0011 | t0001 | g0419 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0420 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0307 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03516 | hp2 | a0002 | c0003 | t0002 | g0269 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03540 | hp1 | a0001 | c0018 | t0002 | g0156 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03579 | hp1 | a0003 | c0009 | t0004 | g0028 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03654 | hp1 | a0001 | c0004 | t0006 | g0148 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0343 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0123 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0166 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0216 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03710 | hp1 | a0012 | c0019 | t0004 | g0070 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0377 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0164 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03927 | hp1 | a0001 | c0004 | t0006 | g0179 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0036 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0351 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0201 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0144 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0406 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0341 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0378 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04199 | hp2 | a0001 | c0004 | t0006 | g0251 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0145 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0211 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18522 | hp1 | a0006 | c0013 | t0009 | g0158 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18612 | hp1 | a0001 | c0001 | t0014 | g0098 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0362 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0266 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0426 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18944 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0404 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0399 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18952 | hp1 | a0002 | c0003 | t0002 | g0152 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18956 | hp2 | a0002 | c0003 | t0002 | g0135 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0383 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0408 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0395 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18972 | hp2 | a0001 | c0004 | t0006 | g0116 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18974 | hp2 | a0005 | c0008 | t0004 | g0006 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0413 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0387 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0391 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18981 | hp2 | a0002 | c0003 | t0002 | g0112 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18984 | hp1 | a0001 | c0001 | t0017 | g0390 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0115 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0411 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18992 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0260 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0365 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0396 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18999 | hp2 | a0002 | c0003 | t0002 | g0078 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19002 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0412 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19003 | hp1 | a0002 | c0003 | t0002 | g0259 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0398 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19009 | hp1 | a0001 | c0001 | t0013 | g0372 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19011 | hp2 | a0001 | c0001 | t0011 | g0076 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19043 | hp1 | a0002 | c0003 | t0005 | g0033 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0292 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0394 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19058 | hp1 | a0001 | c0012 | t0002 | g0095 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19059 | hp2 | a0005 | c0008 | t0004 | g0006 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19067 | hp1 | a0002 | c0003 | t0002 | g0249 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0401 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0380 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0402 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0410 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0222 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0429 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20129 | hp1 | a0002 | c0011 | t0005 | g0418 | AFR | ASW | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20129 | hp2 | a0002 | c0003 | t0002 | g0011 | AFR | ASW | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0113 | EUR | TSI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0165 | EUR | TSI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0326 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02109 | hp1 | a0002 | c0003 | t0002 | g0012 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0331 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0416 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03471 | hp2 | a0003 | c0005 | t0004 | g0432 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0195 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0232 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0430 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0253 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0281 | REF | REF | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0020 | g0414 | REF | REF | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6800331
|
G | A | 1 | a0005 | 2 | NA18974.hp2 NA19059.hp2 |
missense_variant | MODERATE | c.74G>A | p.Gly25Glu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/10 | 276/3049 | 74/1377 | 25/458 | chr12 | 6800331 | ||
| chr12:6814791
|
G | T | 1 | a0012 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.406G>T | p.Gly136Trp | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 608/3049 | 406/1377 | 136/458 | chr12 | 6814791 | ||
| chr12:6814828
|
G | A | 1 | a0006 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.443G>A | p.Gly148Asp | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 645/3049 | 443/1377 | 148/458 | chr12 | 6814828 | ||
| chr12:6814956
|
A | G | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.571A>G | p.Lys191Glu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 773/3049 | 571/1377 | 191/458 | chr12 | 6814956 | ||
| chr12:6816128
|
T | C | 2 | a0003a0007 | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
missense_variant | MODERATE | c.680T>C | p.Phe227Ser | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 882/3049 | 680/1377 | 227/458 | chr12 | 6816128 | ||
| chr12:6816241
|
C | T | 2 | a0002a0011 | 41 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(38): Show |
missense_variant | MODERATE | c.793C>T | p.Arg265Trp | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 995/3049 | 793/1377 | 265/458 | chr12 | 6816241 | ||
| chr12:6817235
|
G | A | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1061G>A | p.Arg354Gln | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/10 | 1263/3049 | 1061/1377 | 354/458 | chr12 | 6817235 | ||
| chr12:6818499
|
T | C | 2 | a0010a0011 | 2 | HG01891.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.1235T>C | p.Ile412Thr | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/10 | 1437/3049 | 1235/1377 | 412/458 | chr12 | 6818499 | ||
| chr12:6818538
|
G | A | 1 | a0009 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1274G>A | p.Arg425Gln | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/10 | 1476/3049 | 1274/1377 | 425/458 | chr12 | 6818538 | ||
| chr12:6818860
|
G | A | 1 | a0004 | 3 | HG02071.hp1 HG02074.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.1292G>A | p.Arg431Gln | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/10 | 1494/3049 | 1292/1377 | 431/458 | chr12 | 6818860 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6800441
|
C | T | 1 | a0002c0011 | 2 | HG03486.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.184C>T | p.Leu62Leu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/10 | 386/3049 | 184/1377 | 62/458 | chr12 | 6800441 | ||
| chr12:6814278
|
G | A | 1 | a0001c0012 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.351G>A | p.Glu117Glu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/10 | 553/3049 | 351/1377 | 117/458 | chr12 | 6814278 | ||
| chr12:6814296
|
C | T | 2 | a0003c0005a0007c0020 | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
synonymous_variant | LOW | c.369C>T | p.Phe123Phe | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/10 | 571/3049 | 369/1377 | 123/458 | chr12 | 6814296 | ||
| chr12:6814943
|
C | T | 1 | a0001c0006 | 4 | HG00639.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.558C>T | p.Val186Val | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 760/3049 | 558/1377 | 186/458 | chr12 | 6814943 | ||
| chr12:6816147
|
G | T | 3 | a0003c0005a0003c0009a0007c0020 | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
synonymous_variant | LOW | c.699G>T | p.Thr233Thr | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 901/3049 | 699/1377 | 233/458 | chr12 | 6816147 | ||
| chr12:6816156
|
C | T | 1 | a0001c0018 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.708C>T | p.Gly236Gly | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 910/3049 | 708/1377 | 236/458 | chr12 | 6816156 | ||
| chr12:6817197
|
T | C | 18 | a0001c0001a0001c0004a0001c0006others(15): Show | 362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
synonymous_variant | LOW | c.1023T>C | p.Ser341Ser | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/10 | 1225/3049 | 1023/1377 | 341/458 | chr12 | 6817197 | ||
| chr12:6817254
|
G | A | 1 | a0008c0014 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1080G>A | p.Val360Val | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/10 | 1282/3049 | 1080/1377 | 360/458 | chr12 | 6817254 | ||
| chr12:6818909
|
T | C | 19 | a0001c0001a0001c0004a0001c0006others(16): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
synonymous_variant | LOW | c.1341T>C | p.Cys447Cys | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/10 | 1543/3049 | 1341/1377 | 447/458 | chr12 | 6818909 | ||
| chr12:6819320
|
C | T | 1 | a0001c0004 | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
synonymous_variant | LOW | c.1368C>T | p.Ser456Ser | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1570/3049 | 1368/1377 | 456/458 | chr12 | 6819320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6819384
|
T | TTCCTGCC others(11): Show |
1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57_*74dupCCTGCCTG others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 75 | INFO_REALIGN_3_PRIME | chr12 | 6819384 | ||||
| chr12:6819403
|
T | A | 9 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(6): Show | 70 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*74T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 74 | chr12 | 6819403 | |||||
| chr12:6819420
|
C | A | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 91 | chr12 | 6819420 | |||||
| chr12:6819421
|
A | G | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
3_prime_UTR_variant | MODIFIER | c.*92A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 92 | chr12 | 6819421 | |||||
| chr12:6819454
|
T | C | 1 | a0001c0001t0013 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 125 | chr12 | 6819454 | |||||
| chr12:6819581
|
T | C | 4 | a0001c0001t0003a0001c0002t0003a0001c0002t0008others(1): Show | 81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*252T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 252 | chr12 | 6819581 | |||||
| chr12:6819614
|
T | A | 2 | a0002c0003t0005a0002c0011t0005 | 7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 285 | chr12 | 6819614 | |||||
| chr12:6819626
|
G | C | 1 | a0001c0001t0014 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 297 | chr12 | 6819626 | |||||
| chr12:6819670
|
G | T | 1 | a0010c0015t0019 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 341 | chr12 | 6819670 | |||||
| chr12:6819739
|
A | G | 12 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(9): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*410A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 410 | chr12 | 6819739 | |||||
| chr12:6819747
|
A | G | 12 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(9): Show | 146 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*418A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 418 | chr12 | 6819747 | |||||
| chr12:6819827
|
C | CCA | 2 | a0002c0003t0005a0002c0011t0005 | 7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*499_*500insAC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 500 | INFO_REALIGN_3_PRIME | chr12 | 6819827 | ||||
| chr12:6819852
|
A | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(18): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*523A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 523 | chr12 | 6819852 | |||||
| chr12:6820060
|
G | A | 1 | a0002c0003t0007 | 4 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*731G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 731 | chr12 | 6820060 | |||||
| chr12:6820092
|
A | G | 1 | a0001c0002t0008 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*763A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 763 | chr12 | 6820092 | |||||
| chr12:6820313
|
C | G | 2 | a0001c0001t0009a0006c0013t0009 | 2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*984C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 984 | chr12 | 6820313 | |||||
| chr12:6820347
|
C | T | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(6): Show | 143 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1018C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1018 | chr12 | 6820347 | |||||
| chr12:6820471
|
T | C | 10 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(7): Show | 144 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1142T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1142 | chr12 | 6820471 | |||||
| chr12:6820494
|
G | A | 2 | a0001c0001t0009a0006c0013t0009 | 2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1165G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1165 | chr12 | 6820494 | |||||
| chr12:6820645
|
CTTTTCCC others(3): Show |
C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319_*1328delTTCC others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1319 | INFO_REALIGN_3_PRIME | chr12 | 6820645 | ||||
| chr12:6820670
|
G | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1341 | chr12 | 6820670 | |||||
| chr12:6820674
|
T | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1345 | chr12 | 6820674 | |||||
| chr12:6820718
|
G | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1389 | chr12 | 6820718 | |||||
| chr12:6820723
|
C | T | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1394 | chr12 | 6820723 | |||||
| chr12:6820746
|
G | A | 3 | a0001c0004t0006a0002c0003t0005a0002c0011t0005 | 14 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1417G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1417 | chr12 | 6820746 | |||||
| chr12:6820790
|
A | G | 1 | a0002c0003t0018 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1461 | chr12 | 6820790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6789680
|
G | A | 1 | a0001c0006t0001g0008 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-68+18G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789680 | ||||||
| chr12:6789703
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-68+41G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789703 | ||||||
| chr12:6789791
|
G | C | 4 | a0001c0001t0004g0010a0001c0001t0004g0013a0002c0003t0002g0011others(1): Show | 4 | HG02109.hp1 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+129G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789791 | ||||||
| chr12:6789862
|
C | T | 9 | a0001c0001t0004g0007a0001c0002t0003g0430a0002c0003t0001g0429others(6): Show | 10 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-68+200C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789862 | ||||||
| chr12:6789890
|
A | G | 14 | a0001c0001t0004g0425a0001c0001t0004g0426a0001c0010t0003g0422others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.-68+228A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789890 | ||||||
| chr12:6790015
|
T | G | 335 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(332): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.-68+353T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790015 | ||||||
| chr12:6790020
|
G | C | 22 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(19): Show | 22 | HG01109.hp2 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68+358G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790020 | ||||||
| chr12:6790056
|
A | G | 13 | a0001c0001t0001g0316a0001c0001t0001g0319a0001c0001t0002g0004others(10): Show | 14 | HG01106.hp1 HG01109.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.-68+394A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790056 | ||||||
| chr12:6790080
|
T | C | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+418T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790080 | ||||||
| chr12:6790142
|
C | CG | 211 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(208): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-68+480_-68+481ins others(1): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790142 | ||||||
| chr12:6790212
|
CT | C | 433 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(430): Show | 440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.-68+552delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6790212 | |||||
| chr12:6790342
|
G | A | 189 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.-68+680G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790342 | ||||||
| chr12:6790360
|
G | A | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-68+698G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790360 | ||||||
| chr12:6790362
|
T | C | 189 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.-68+700T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790362 | ||||||
| chr12:6790416
|
T | C | 132 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(129): Show | 135 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-68+754T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790416 | ||||||
| chr12:6790524
|
A | C | 36 | a0001c0001t0001g0381a0001c0001t0001g0382a0001c0001t0001g0384others(33): Show | 38 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.-68+862A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790524 | ||||||
| chr12:6790526
|
C | T | 1 | a0001c0002t0003g0307 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-68+864C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790526 | ||||||
| chr12:6790631
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-68+969T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790631 | ||||||
| chr12:6790721
|
C | T | 6 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0001g0305others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+1059C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790721 | ||||||
| chr12:6790722
|
G | A | 1 | a0001c0004t0006g0148 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-68+1060G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790722 | ||||||
| chr12:6790941
|
T | C | 1 | a0001c0002t0003g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-68+1279T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790941 | ||||||
| chr12:6791193
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-68+1531C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791193 | ||||||
| chr12:6791194
|
G | C | 1 | a0001c0001t0002g0038 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-68+1532G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791194 | ||||||
| chr12:6791378
|
G | T | 1 | a0001c0001t0001g0379 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-68+1716G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791378 | ||||||
| chr12:6791399
|
C | G | 159 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.-68+1737C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791399 | ||||||
| chr12:6791447
|
T | C | 119 | a0001c0001t0001g0045a0001c0001t0001g0153a0001c0001t0001g0154others(116): Show | 120 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-68+1785T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791447 | ||||||
| chr12:6791450
|
A | G | 142 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(139): Show | 144 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-68+1788A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791450 | ||||||
| chr12:6791502
|
C | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-68+1840C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791502 | ||||||
| chr12:6791508
|
G | A | 1 | a0007c0020t0004g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-68+1846G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791508 | ||||||
| chr12:6791602
|
C | T | 1 | a0002c0003t0007g0427 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-68+1940C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791602 | ||||||
| chr12:6791629
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+1967C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791629 | ||||||
| chr12:6791636
|
T | C | 3 | a0001c0001t0004g0013a0002c0003t0002g0011a0002c0003t0002g0012 | 3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-68+1974T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791636 | ||||||
| chr12:6791722
|
C | T | 10 | a0001c0001t0004g0007a0001c0001t0004g0010a0001c0002t0003g0430others(7): Show | 11 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-68+2060C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791722 | ||||||
| chr12:6791860
|
C | T | 1 | a0001c0001t0001g0413 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-68+2198C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791860 | ||||||
| chr12:6791898
|
G | T | 1 | a0001c0001t0002g0261 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-68+2236G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791898 | ||||||
| chr12:6791911
|
A | G | 303 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(300): Show | 308 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-68+2249A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791911 | ||||||
| chr12:6791916
|
G | A | 338 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(335): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.-68+2254G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791916 | ||||||
| chr12:6791964
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG01168.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-68+2302G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791964 | ||||||
| chr12:6791968
|
C | T | 121 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(118): Show | 122 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-68+2306C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791968 | ||||||
| chr12:6792154
|
G | A | 1 | a0001c0002t0003g0272 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-68+2492G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792154 | ||||||
| chr12:6792236
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0004g0271others(5): Show | 8 | HG02145.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-68+2574G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792236 | ||||||
| chr12:6792285
|
G | A | 1 | a0001c0002t0003g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-68+2623G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792285 | ||||||
| chr12:6792300
|
C | T | 2 | a0002c0003t0002g0259a0002c0003t0002g0260 | 2 | NA18993.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-68+2638C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792300 | ||||||
| chr12:6792440
|
C | CT | 28 | a0001c0001t0001g0009a0001c0001t0001g0353a0001c0001t0001g0354others(25): Show | 28 | HG00408.hp2 HG00621.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.-68+2785dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6792440 | |||||
| chr12:6792508
|
A | G | 12 | a0001c0001t0004g0425a0001c0001t0004g0426a0001c0010t0003g0422others(9): Show | 12 | HG01358.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-68+2846A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792508 | ||||||
| chr12:6792594
|
C | T | 1 | a0001c0002t0003g0258 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-68+2932C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792594 | ||||||
| chr12:6792613
|
C | T | 5 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+2951C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792613 | ||||||
| chr12:6792657
|
G | A | 150 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(147): Show | 152 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-68+2995G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792657 | ||||||
| chr12:6792663
|
G | T | 1 | a0001c0010t0003g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-68+3001G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792663 | ||||||
| chr12:6792716
|
C | G | 1 | a0001c0001t0001g0323 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-68+3054C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792716 | ||||||
| chr12:6792836
|
G | T | 280 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(277): Show | 284 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-68+3174G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792836 | ||||||
| chr12:6793087
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-68+3425C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793087 | ||||||
| chr12:6793411
|
C | T | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(4): Show | 7 | HG00423.hp2 NA18963.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+3749C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793411 | ||||||
| chr12:6793506
|
C | G | 1 | a0001c0001t0004g0426 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-68+3844C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793506 | ||||||
| chr12:6793637
|
GTATCTAT others(8): Show |
G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-68+3988_-68+4002d others(17): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793637 | |||||
| chr12:6793649
|
CATCT | C | 34 | a0001c0001t0001g0153a0001c0001t0001g0268a0001c0001t0001g0301others(31): Show | 34 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-68+4040_-68+4043d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | |||||
| chr12:6793649
|
CATCTATC others(1): Show |
C | 85 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0047others(82): Show | 88 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4043d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | |||||
| chr12:6793649
|
CATCTATC others(5): Show |
C | 22 | a0001c0001t0001g0325a0001c0001t0001g0344a0001c0001t0001g0345others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68+4032_-68+4043d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | |||||
| chr12:6793649
|
CATCTATC others(9): Show |
C | 3 | a0001c0001t0001g0352a0001c0001t0001g0378a0001c0002t0003g0351 | 3 | HG02129.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-68+4028_-68+4043d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | |||||
| chr12:6793685
|
TATCTATC others(10): Show |
T | 4 | a0001c0001t0001g0035a0001c0001t0004g0034a0002c0003t0002g0032others(1): Show | 4 | HG02622.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4024_-68+4040d others(19): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793685 | ||||||
| chr12:6793688
|
CTATCTAT others(7): Show |
C | 101 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0077others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-68+4028_-68+4041d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793688 | |||||
| chr12:6793689
|
TATCTATC others(6): Show |
T | 11 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145others(8): Show | 11 | HG01192.hp1 HG01891.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+4028_-68+4040d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793689 | ||||||
| chr12:6793689
|
TATCTATC others(8): Show |
T | 1 | a0001c0004t0006g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-68+4028_-68+4042d others(17): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793689 | ||||||
| chr12:6793692
|
CTATCTAT others(3): Show |
C | 91 | a0001c0001t0001g0042a0001c0001t0001g0059a0001c0001t0001g0065others(88): Show | 92 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-68+4032_-68+4041d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793692 | |||||
| chr12:6793693
|
TATCTATC others(2): Show |
T | 11 | a0001c0001t0001g0019a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01358.hp1 HG01993.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+4032_-68+4040d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793693 | ||||||
| chr12:6793693
|
TATCTATC others(4): Show |
T | 2 | a0001c0001t0001g0045a0003c0005t0004g0434 | 2 | HG01169.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-68+4032_-68+4042d others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793693 | ||||||
| chr12:6793696
|
CTATCTA | C | 30 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(27): Show | 30 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4041d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793696 | |||||
| chr12:6793697
|
TATCTA | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4040d others(7): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793697 | ||||||
| chr12:6793697
|
TATCTATC | T | 4 | a0001c0001t0001g0155a0001c0001t0004g0157a0001c0018t0002g0156others(1): Show | 4 | HG01928.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4042d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793697 | ||||||
| chr12:6793702
|
A | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0268a0002c0003t0002g0424others(1): Show | 4 | HG01884.hp2 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+4040A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793702 | ||||||
| chr12:6793704
|
C | T | 264 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(261): Show | 268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.-68+4042C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793704 | ||||||
| chr12:6793716
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-68+4054T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793716 | ||||||
| chr12:6793738
|
G | A | 1 | a0001c0001t0004g0007 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-68+4076G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793738 | ||||||
| chr12:6793758
|
G | A | 7 | a0001c0001t0004g0003a0001c0001t0004g0245a0001c0001t0004g0246others(4): Show | 8 | HG01192.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-68+4096G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793758 | ||||||
| chr12:6793798
|
C | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(10): Show | 13 | HG01109.hp2 HG01993.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-68+4136C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793798 | ||||||
| chr12:6793831
|
T | C | 2 | a0001c0001t0001g0328a0001c0001t0001g0332 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-68+4169T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793831 | ||||||
| chr12:6793888
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-68+4226A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793888 | ||||||
| chr12:6793958
|
TTCTATCT others(7): Show |
T | 3 | a0001c0001t0004g0013a0002c0003t0002g0011a0002c0003t0002g0012 | 3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-68+4310_-68+4323d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793958 | |||||
| chr12:6793960
|
CTATCTAT others(3): Show |
C | 4 | a0001c0001t0002g0320a0001c0001t0002g0321a0001c0001t0002g0343others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4310_-68+4319d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793960 | |||||
| chr12:6793964
|
CTATCTA | C | 9 | a0001c0001t0001g0358a0001c0001t0001g0366a0001c0001t0001g0405others(6): Show | 9 | HG02040.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+4310_-68+4315d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793964 | |||||
| chr12:6793968
|
CTA | C | 127 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-68+4310_-68+4311d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793968 | |||||
| chr12:6793970
|
A | ATATC | 4 | a0001c0001t0001g0185a0001c0001t0002g0184a0001c0001t0004g0041others(1): Show | 4 | HG00741.hp1 HG02258.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4341_-68+4344d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATATCTAT others(1): Show |
118 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(115): Show | 120 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-68+4337_-68+4344d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATATCTAT others(5): Show |
62 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0122others(59): Show | 64 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-68+4333_-68+4344d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATATCTAT others(9): Show |
63 | a0001c0001t0001g0045a0001c0001t0001g0071a0001c0001t0001g0127others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-68+4329_-68+4344d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATATCTAT others(13): Show |
7 | a0001c0001t0002g0134a0001c0001t0002g0136a0001c0001t0002g0137others(4): Show | 7 | HG01167.hp1 HG01192.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+4325_-68+4344d others(22): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATATCTAT others(17): Show |
5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0240others(2): Show | 5 | HG02135.hp1 HG03704.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+4321_-68+4344d others(26): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATATCTAT others(21): Show |
1 | a0001c0001t0002g0289 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-68+4317_-68+4344d others(30): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATC | 22 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0268others(19): Show | 22 | HG00408.hp2 HG01993.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68+4309_-68+4310i others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6793970
|
A | ATCTATC | 7 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0352others(4): Show | 7 | HG02129.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+4309_-68+4310i others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | |||||
| chr12:6794030
|
ATCTG | A | 32 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(29): Show | 32 | HG01109.hp2 HG01358.hp1 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.-68+4372_-68+4375d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794030 | |||||
| chr12:6794075
|
C | CTATCTTT others(5): Show |
1 | a0001c0001t0001g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-68+4415_-68+4426d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794075 | |||||
| chr12:6794079
|
CT | C | 22 | a0001c0001t0001g0139a0001c0001t0001g0161a0001c0001t0001g0186others(19): Show | 22 | HG00673.hp2 HG01167.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-68+4430delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794079 | |||||
| chr12:6794088
|
T | TG | 3 | a0001c0001t0001g0040a0001c0001t0003g0039a0002c0003t0002g0424 | 3 | HG01884.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-68+4426_-68+4427i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794088 | ||||||
| chr12:6794142
|
G | T | 116 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0065others(113): Show | 119 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-68+4480G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794142 | ||||||
| chr12:6794165
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0003g0039a0001c0002t0003g0222others(1): Show | 4 | HG01884.hp2 HG03139.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+4503C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794165 | ||||||
| chr12:6794465
|
G | A | 36 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0277others(33): Show | 37 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.-68+4803G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794465 | ||||||
| chr12:6794468
|
T | G | 4 | a0001c0001t0004g0013a0001c0002t0003g0430a0002c0003t0002g0011others(1): Show | 4 | HG02109.hp1 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4806T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794468 | ||||||
| chr12:6794521
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-68+4859G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794521 | ||||||
| chr12:6794599
|
C | T | 7 | a0001c0001t0001g0065a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | NA18943.hp2 NA18977.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+4937C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794599 | ||||||
| chr12:6794604
|
TC | T | 3 | a0001c0001t0001g0368a0001c0001t0001g0377a0001c0001t0004g0367 | 3 | HG02015.hp1 HG02027.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-68+4943delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794604 | ||||||
| chr12:6794724
|
C | T | 2 | a0001c0002t0003g0238a0001c0002t0003g0239 | 2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-68+5062C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794724 | ||||||
| chr12:6794765
|
C | A | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5103C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794765 | ||||||
| chr12:6794769
|
A | C | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5107A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794769 | ||||||
| chr12:6794773
|
C | T | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5111C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794773 | ||||||
| chr12:6794775
|
G | GTTTTTTT others(2): Show |
7 | a0001c0001t0001g0224a0001c0001t0001g0240a0001c0001t0001g0263others(4): Show | 7 | HG01256.hp1 HG02897.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+5115_-68+5123d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | GTTTTTTT others(3): Show |
31 | a0001c0001t0001g0122a0001c0001t0001g0162a0001c0001t0001g0228others(28): Show | 32 | HG00140.hp2 HG01081.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.-68+5114_-68+5123d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | GTTTTTTT others(4): Show |
46 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0182others(43): Show | 46 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | GTTTTTTT others(5): Show |
31 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(28): Show | 31 | HG00673.hp1 HG01074.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | GTTTTTTT others(6): Show |
7 | a0001c0001t0001g0161a0001c0001t0001g0212a0001c0001t0002g0236others(4): Show | 7 | HG00673.hp2 HG01261.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0004g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-68+5123_-68+5124i others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | GTTTTTTT others(8): Show |
2 | a0001c0001t0001g0237a0001c0001t0002g0213 | 2 | HG00323.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(17): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | |||||
| chr12:6794775
|
G | T | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5113G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794775 | ||||||
| chr12:6794776
|
T | G | 97 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0045others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-68+5114T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794776 | ||||||
| chr12:6794780
|
TTTTTTG | T | 9 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+5124_-68+5129d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794780 | |||||
| chr12:6794785
|
TG | T | 3 | a0001c0001t0001g0191a0001c0001t0002g0190a0001c0001t0002g0217 | 3 | HG01069.hp2 HG02293.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-68+5124delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794785 | ||||||
| chr12:6794786
|
G | GT | 29 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0059others(26): Show | 29 | HG00438.hp1 HG00597.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-68+5140dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | |||||
| chr12:6794786
|
G | GTT | 6 | a0001c0001t0001g0102a0001c0001t0002g0073a0001c0001t0002g0100others(3): Show | 6 | HG00597.hp1 HG03831.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-68+5139_-68+5140d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | |||||
| chr12:6794786
|
G | T | 130 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(127): Show | 131 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-68+5124G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794786 | ||||||
| chr12:6794786
|
GTT | G | 10 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(7): Show | 10 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-68+5139_-68+5140d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | |||||
| chr12:6794786
|
GTTT | G | 11 | a0001c0001t0004g0425a0001c0001t0004g0426a0001c0010t0003g0422others(8): Show | 11 | HG01358.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-68+5138_-68+5140d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | |||||
| chr12:6794803
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-68+5141G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794803 | ||||||
| chr12:6794823
|
C | T | 143 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(140): Show | 144 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-68+5161C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794823 | ||||||
| chr12:6794980
|
T | G | 33 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0277others(30): Show | 33 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-67-5092T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794980 | ||||||
| chr12:6795070
|
G | A | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-67-5002G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795070 | ||||||
| chr12:6795098
|
C | CTCTA | 190 | a0001c0001t0001g0009a0001c0001t0001g0045a0001c0001t0001g0059others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-67-4937_-67-4934d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795098
|
C | CTCTATCT others(1): Show |
164 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-67-4941_-67-4934d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795098
|
C | CTCTATCT others(5): Show |
28 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0161others(25): Show | 28 | HG00558.hp1 HG00642.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-67-4945_-67-4934d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795098
|
C | CTCTATCT others(9): Show |
7 | a0001c0001t0001g0221a0001c0001t0001g0240a0001c0001t0001g0368others(4): Show | 7 | HG02015.hp1 HG02148.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-4949_-67-4934d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795098
|
C | CTCTATCT others(13): Show |
1 | a0001c0001t0004g0183 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-67-4953_-67-4934d others(22): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795098
|
C | CTCTATCT others(5): Show |
2 | a0001c0001t0002g0169a0001c0001t0002g0175 | 2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-67-4965_-67-4964i others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795098
|
CTCTA | C | 4 | a0001c0001t0001g0200a0001c0001t0004g0003a0001c0001t0004g0245others(1): Show | 5 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-4937_-67-4934d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | |||||
| chr12:6795100
|
C | G | 1 | a0009c0016t0001g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-67-4972C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795100 | ||||||
| chr12:6795102
|
A | C | 1 | a0009c0016t0001g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-67-4970A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795102 | ||||||
| chr12:6795316
|
A | T | 1 | a0001c0001t0004g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67-4756A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795316 | ||||||
| chr12:6795317
|
CCTGT | C | 135 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(132): Show | 136 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.-67-4752_-67-4749d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795317 | |||||
| chr12:6795457
|
C | T | 1 | a0001c0004t0006g0116 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-67-4615C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795457 | ||||||
| chr12:6795624
|
C | T | 21 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0277others(18): Show | 21 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-67-4448C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795624 | ||||||
| chr12:6795679
|
A | T | 7 | a0001c0002t0003g0430a0003c0005t0004g0431a0003c0005t0004g0432others(4): Show | 7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-4393A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795679 | ||||||
| chr12:6795900
|
C | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0223 | 2 | NA19080.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-67-4172C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795900 | ||||||
| chr12:6795955
|
T | G | 1 | a0001c0001t0004g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67-4117T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795955 | ||||||
| chr12:6795959
|
C | A | 1 | a0001c0001t0004g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67-4113C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795959 | ||||||
| chr12:6795962
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-67-4110C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795962 | ||||||
| chr12:6796015
|
T | C | 202 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(199): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.-67-4057T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796015 | ||||||
| chr12:6796098
|
C | T | 191 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(188): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-67-3974C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796098 | ||||||
| chr12:6796118
|
A | G | 2 | a0001c0001t0004g0271a0002c0003t0002g0270 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-67-3954A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796118 | ||||||
| chr12:6796251
|
T | C | 303 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(300): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-67-3821T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796251 | ||||||
| chr12:6796384
|
C | G | 202 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(199): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.-67-3688C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796384 | ||||||
| chr12:6796442
|
A | C | 205 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-67-3630A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796442 | ||||||
| chr12:6796524
|
T | A | 11 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(8): Show | 11 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-67-3548T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796524 | ||||||
| chr12:6796549
|
T | C | 205 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-67-3523T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796549 | ||||||
| chr12:6796772
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-67-3300A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796772 | ||||||
| chr12:6796823
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-67-3249G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796823 | ||||||
| chr12:6796945
|
C | T | 8 | a0001c0001t0001g0040a0001c0002t0003g0430a0003c0005t0004g0431others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67-3127C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796945 | ||||||
| chr12:6797133
|
A | G | 13 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(10): Show | 13 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-67-2939A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797133 | ||||||
| chr12:6797153
|
G | A | 137 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(134): Show | 138 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-67-2919G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797153 | ||||||
| chr12:6797312
|
C | A | 1 | a0001c0001t0002g0350 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-67-2760C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797312 | ||||||
| chr12:6797502
|
A | G | 6 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(3): Show | 6 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-2570A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797502 | ||||||
| chr12:6797520
|
C | T | 1 | a0001c0001t0004g0007 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-67-2552C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797520 | ||||||
| chr12:6797527
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2545C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797527 | ||||||
| chr12:6797603
|
G | A | 2 | a0001c0001t0002g0285a0001c0002t0003g0430 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-67-2469G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797603 | ||||||
| chr12:6797643
|
G | C | 5 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2429G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797643 | ||||||
| chr12:6797662
|
T | C | 205 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-67-2410T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797662 | ||||||
| chr12:6797663
|
A | G | 205 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0043others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-67-2409A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797663 | ||||||
| chr12:6797668
|
C | T | 95 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0065others(92): Show | 97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-67-2404C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797668 | ||||||
| chr12:6797769
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0004g0010a0001c0001t0004g0022others(4): Show | 7 | HG01261.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67-2303A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797769 | ||||||
| chr12:6797799
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-67-2273G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797799 | ||||||
| chr12:6797838
|
G | A | 4 | a0001c0001t0004g0013a0001c0010t0003g0422a0002c0003t0002g0011others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-2234G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797838 | ||||||
| chr12:6797860
|
C | T | 94 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0065others(91): Show | 96 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-67-2212C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797860 | ||||||
| chr12:6797967
|
C | T | 1 | a0001c0001t0004g0002 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-67-2105C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797967 | ||||||
| chr12:6798067
|
C | A | 2 | a0001c0001t0001g0356a0001c0001t0001g0369 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-67-2005C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798067 | ||||||
| chr12:6798067
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-67-2005C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798067 | ||||||
| chr12:6798098
|
T | C | 288 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-67-1974T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798098 | ||||||
| chr12:6798123
|
C | T | 125 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(122): Show | 127 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-67-1949C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798123 | ||||||
| chr12:6798139
|
C | T | 2 | a0001c0001t0001g0323a0007c0020t0004g0322 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-67-1933C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798139 | ||||||
| chr12:6798172
|
C | CT | 8 | a0001c0001t0001g0262a0001c0001t0001g0265a0001c0001t0001g0413others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67-1885dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6798172 | |||||
| chr12:6798172
|
CT | C | 6 | a0001c0001t0002g0066a0001c0001t0002g0119a0001c0001t0004g0024others(3): Show | 6 | HG01516.hp1 HG02280.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-1885delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6798172 | |||||
| chr12:6798208
|
C | A | 4 | a0001c0001t0001g0410a0001c0002t0003g0411a0001c0002t0003g0412others(1): Show | 4 | NA18989.hp2 NA19002.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-1864C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798208 | ||||||
| chr12:6798208
|
C | T | 94 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0071others(91): Show | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-67-1864C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798208 | ||||||
| chr12:6798217
|
TGGAGTGC others(249): Show |
T | 37 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0277others(34): Show | 38 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.-67-1853_-67-1598d others(2): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6798217 | |||||
| chr12:6798221
|
G | C | 1 | a0002c0003t0002g0424 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-67-1851G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798221 | ||||||
| chr12:6798230
|
C | T | 5 | a0001c0001t0001g0268a0001c0001t0001g0410a0001c0002t0003g0411others(2): Show | 5 | HG02895.hp2 NA18989.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-1842C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798230 | ||||||
| chr12:6798232
|
C | T | 3 | a0001c0001t0001g0410a0001c0002t0003g0411a0001c0002t0003g0412 | 3 | NA18989.hp2 NA19002.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-67-1840C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798232 | ||||||
| chr12:6798318
|
C | T | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-67-1754C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798318 | ||||||
| chr12:6798330
|
C | A | 3 | a0001c0001t0004g0013a0002c0003t0002g0011a0002c0003t0002g0012 | 3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-67-1742C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798330 | ||||||
| chr12:6798362
|
T | C | 7 | a0001c0001t0004g0147a0001c0001t0004g0302a0001c0001t0004g0426others(4): Show | 7 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-1710T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798362 | ||||||
| chr12:6798364
|
G | T | 1 | a0001c0006t0001g0349 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-67-1708G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798364 | ||||||
| chr12:6798379
|
C | A | 1 | a0001c0002t0003g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-67-1693C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798379 | ||||||
| chr12:6798380
|
A | G | 1 | a0001c0002t0003g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-67-1692A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798380 | ||||||
| chr12:6798449
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-1623C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798449 | ||||||
| chr12:6798480
|
C | T | 1 | a0001c0001t0009g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-67-1592C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798480 | ||||||
| chr12:6798485
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0004g0007a0002c0003t0002g0249 | 4 | HG02257.hp1 HG02280.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-1587G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798485 | ||||||
| chr12:6798564
|
T | A | 5 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-1508T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798564 | ||||||
| chr12:6798602
|
G | C | 7 | a0001c0001t0004g0147a0001c0001t0004g0302a0001c0001t0004g0426others(4): Show | 7 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-1470G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798602 | ||||||
| chr12:6798766
|
C | A | 2 | a0001c0004t0006g0179a0001c0004t0006g0251 | 2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-67-1306C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798766 | ||||||
| chr12:6798805
|
C | G | 1 | a0001c0002t0003g0211 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-67-1267C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798805 | ||||||
| chr12:6798951
|
A | G | 3 | a0001c0001t0004g0013a0002c0003t0002g0011a0002c0003t0002g0012 | 3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-67-1121A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798951 | ||||||
| chr12:6798980
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-1092G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798980 | ||||||
| chr12:6799023
|
C | T | 1 | a0002c0003t0002g0135 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-67-1049C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799023 | ||||||
| chr12:6799027
|
C | T | 1 | a0001c0002t0003g0400 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-67-1045C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799027 | ||||||
| chr12:6799049
|
T | G | 5 | a0001c0001t0001g0040a0001c0001t0003g0018a0001c0001t0003g0039others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-1023T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799049 | ||||||
| chr12:6799059
|
A | G | 4 | a0001c0001t0004g0013a0001c0001t0004g0041a0002c0003t0002g0011others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-1013A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799059 | ||||||
| chr12:6799221
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-67-851A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799221 | ||||||
| chr12:6799231
|
A | T | 1 | a0001c0002t0003g0430 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-67-841A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799231 | ||||||
| chr12:6799298
|
T | C | 2 | a0001c0004t0006g0179a0001c0004t0006g0251 | 2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-67-774T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799298 | ||||||
| chr12:6799357
|
G | A | 289 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-67-715G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799357 | ||||||
| chr12:6799483
|
G | A | 1 | a0001c0002t0003g0165 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-67-589G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799483 | ||||||
| chr12:6799626
|
G | A | 247 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(244): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-67-446G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799626 | ||||||
| chr12:6799637
|
C | T | 2 | a0001c0001t0002g0282a0001c0006t0001g0336 | 2 | HG01175.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-67-435C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799637 | ||||||
| chr12:6799641
|
C | T | 1 | a0001c0001t0012g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-67-431C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799641 | ||||||
| chr12:6799713
|
G | A | 3 | a0001c0001t0001g0250a0001c0001t0002g0213a0001c0002t0003g0202 | 3 | HG00323.hp2 HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-67-359G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799713 | ||||||
| chr12:6799770
|
C | T | 273 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(270): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-67-302C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799770 | ||||||
| chr12:6799900
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-67-172C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799900 | ||||||
| chr12:6800214
|
TG | T | 253 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.49+28delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800214 | ||||||
| chr12:6800222
|
A | G | 423 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(420): Show | 430 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(427): Show |
intron_variant | MODIFIER | c.49+35A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800222 | ||||||
| chr12:6800269
|
G | A | 3 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0292 | 3 | HG01891.hp2 HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.50-38G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800269 | ||||||
| chr12:6800276
|
T | C | 268 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(265): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.50-31T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800276 | ||||||
| chr12:6800504
|
A | G | 1 | a0001c0001t0004g0403 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.214+33A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800504 | ||||||
| chr12:6800605
|
T | C | 1 | a0001c0001t0004g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.214+134T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800605 | ||||||
| chr12:6800735
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.214+264C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800735 | ||||||
| chr12:6800759
|
A | G | 1 | a0008c0014t0016g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.214+288A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800759 | ||||||
| chr12:6800763
|
AC | A | 5 | a0001c0001t0004g0302a0002c0003t0007g0027a0002c0003t0007g0417others(2): Show | 5 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+294delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6800763 | |||||
| chr12:6800778
|
A | G | 4 | a0001c0001t0004g0013a0001c0010t0003g0422a0002c0003t0002g0011others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+307A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800778 | ||||||
| chr12:6800807
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.214+336C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800807 | ||||||
| chr12:6800812
|
A | G | 1 | a0003c0009t0004g0428 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214+341A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800812 | ||||||
| chr12:6800904
|
AT | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0162a0001c0001t0001g0252others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+434delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800904 | ||||||
| chr12:6800905
|
T | A | 262 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.214+434T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800905 | ||||||
| chr12:6800907
|
T | A | 15 | a0001c0001t0001g0162a0001c0001t0001g0252a0001c0001t0002g0073others(12): Show | 15 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+436T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800907 | ||||||
| chr12:6800914
|
AT | A | 12 | a0001c0001t0004g0293a0001c0002t0003g0020a0001c0002t0003g0021others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+451delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6800914 | |||||
| chr12:6800916
|
T | A | 29 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0040others(26): Show | 29 | HG00735.hp1 HG01261.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.214+445T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800916 | ||||||
| chr12:6800974
|
C | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0162a0001c0001t0001g0252others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+503C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800974 | ||||||
| chr12:6801121
|
G | C | 8 | a0001c0001t0004g0041a0002c0003t0001g0429a0003c0005t0004g0431others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+650G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801121 | ||||||
| chr12:6801152
|
C | T | 1 | a0001c0002t0003g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.214+681C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801152 | ||||||
| chr12:6801213
|
A | T | 9 | a0001c0001t0001g0162a0001c0001t0001g0252a0002c0003t0002g0249others(6): Show | 9 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+742A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801213 | ||||||
| chr12:6801225
|
A | T | 1 | a0003c0009t0004g0428 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214+754A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801225 | ||||||
| chr12:6801257
|
C | A | 14 | a0001c0001t0001g0154a0001c0001t0001g0353a0001c0001t0001g0354others(11): Show | 14 | HG00408.hp2 HG00621.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.214+786C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801257 | ||||||
| chr12:6801264
|
T | C | 3 | a0001c0001t0012g0052a0002c0003t0001g0429a0008c0014t0016g0264 | 3 | HG01884.hp1 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.214+793T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801264 | ||||||
| chr12:6801295
|
T | C | 1 | a0001c0001t0004g0126 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.214+824T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801295 | ||||||
| chr12:6801299
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.214+828C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801299 | ||||||
| chr12:6801300
|
G | A | 28 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0176others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+829G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801300 | ||||||
| chr12:6801302
|
N | A | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+831C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801302 | ||||||
| chr12:6801343
|
C | A | 8 | a0001c0001t0004g0147a0001c0001t0004g0302a0001c0001t0004g0426others(5): Show | 8 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+872C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801343 | ||||||
| chr12:6801343
|
C | T | 1 | a0001c0001t0009g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214+872C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801343 | ||||||
| chr12:6801377
|
T | C | 1 | a0001c0001t0001g0384 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.214+906T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801377 | ||||||
| chr12:6801382
|
G | T | 312 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(309): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.214+911G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801382 | ||||||
| chr12:6801384
|
G | T | 1 | a0001c0002t0003g0234 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.214+913G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801384 | ||||||
| chr12:6801399
|
T | C | 301 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(298): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.214+928T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801399 | ||||||
| chr12:6801494
|
G | A | 215 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.214+1023G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801494 | ||||||
| chr12:6801516
|
C | CA | 92 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(89): Show | 93 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.214+1060dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801516 | |||||
| chr12:6801516
|
C | CAA | 6 | a0001c0001t0001g0153a0001c0001t0002g0181a0001c0001t0004g0108others(3): Show | 6 | HG02132.hp2 HG04228.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+1059_214+1060d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801516 | |||||
| chr12:6801516
|
CA | C | 127 | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0043others(124): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.214+1060delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801516 | |||||
| chr12:6801538
|
N | G | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+1067A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801538 | ||||||
| chr12:6801540
|
TTTA | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(16): Show | 19 | HG01109.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.214+1085_214+1087d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801540 | |||||
| chr12:6801558
|
AGTTT | A | 12 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0132others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+1088_214+1091d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801558 | ||||||
| chr12:6801593
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.214+1122T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801593 | ||||||
| chr12:6801598
|
T | C | 1 | a0002c0003t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.214+1127T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801598 | ||||||
| chr12:6801599
|
C | T | 7 | a0001c0001t0001g0268a0002c0003t0001g0416a0002c0003t0001g0420others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+1128C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801599 | ||||||
| chr12:6801600
|
G | A | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+1129G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801600 | ||||||
| chr12:6801615
|
C | T | 8 | a0001c0001t0001g0268a0001c0010t0003g0422a0002c0003t0001g0416others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+1144C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801615 | ||||||
| chr12:6801616
|
G | A | 360 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(357): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.214+1145G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801616 | ||||||
| chr12:6801708
|
A | G | 4 | a0001c0001t0003g0018a0001c0001t0003g0039a0001c0001t0004g0302others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1237A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801708 | ||||||
| chr12:6801717
|
T | C | 2 | a0001c0001t0001g0405a0001c0001t0004g0293 | 2 | HG02738.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.214+1246T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801717 | ||||||
| chr12:6801718
|
G | A | 1 | a0001c0001t0001g0405 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.214+1247G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801718 | ||||||
| chr12:6801753
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0004g0010a0001c0001t0004g0022others(3): Show | 6 | HG01261.hp1 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+1282A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801753 | ||||||
| chr12:6801767
|
A | G | 91 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0042others(88): Show | 93 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.214+1296A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801767 | ||||||
| chr12:6801769
|
C | T | 2 | a0001c0001t0002g0169a0001c0001t0002g0175 | 2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.214+1298C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801769 | ||||||
| chr12:6801774
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG02572.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+1303C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801774 | ||||||
| chr12:6801778
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG02572.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+1307T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801778 | ||||||
| chr12:6801817
|
C | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG02630.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.214+1346C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801817 | ||||||
| chr12:6801845
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.214+1374T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801845 | ||||||
| chr12:6801903
|
C | T | 5 | a0002c0003t0001g0174a0002c0003t0007g0027a0002c0003t0007g0267others(2): Show | 5 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+1432C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801903 | ||||||
| chr12:6801911
|
T | C | 2 | a0001c0001t0002g0277a0001c0001t0002g0285 | 2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.214+1440T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801911 | ||||||
| chr12:6801942
|
T | C | 1 | a0001c0001t0002g0392 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214+1471T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801942 | ||||||
| chr12:6802036
|
G | T | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+1565G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802036 | ||||||
| chr12:6802122
|
C | T | 1 | a0001c0002t0003g0131 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.214+1651C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802122 | ||||||
| chr12:6802218
|
T | C | 1 | a0001c0001t0004g0219 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.214+1747T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802218 | ||||||
| chr12:6802271
|
T | C | 356 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.214+1800T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802271 | ||||||
| chr12:6802319
|
C | CT | 21 | a0001c0001t0001g0042a0001c0001t0001g0059a0001c0001t0001g0084others(18): Show | 22 | HG01515.hp2 HG01884.hp2 HG03225.hp1 others(19): Show |
intron_variant | MODIFIER | c.214+1863dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6802319 | |||||
| chr12:6802541
|
C | T | 212 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.214+2070C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802541 | ||||||
| chr12:6802617
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0039 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214+2146C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802617 | ||||||
| chr12:6802759
|
C | G | 1 | a0002c0003t0007g0427 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.214+2288C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802759 | ||||||
| chr12:6802759
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.214+2288C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802759 | ||||||
| chr12:6802800
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.214+2329G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802800 | ||||||
| chr12:6803016
|
A | G | 28 | a0001c0001t0001g0155a0001c0001t0001g0323a0001c0001t0002g0190others(25): Show | 29 | HG01928.hp1 HG01978.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.214+2545A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803016 | ||||||
| chr12:6803102
|
A | C | 2 | a0001c0001t0001g0375a0001c0001t0001g0408 | 2 | NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.214+2631A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803102 | ||||||
| chr12:6803151
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.214+2680C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803151 | ||||||
| chr12:6803294
|
G | A | 1 | a0009c0016t0001g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214+2823G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803294 | ||||||
| chr12:6803391
|
T | C | 114 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0155others(111): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.214+2920T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803391 | ||||||
| chr12:6803396
|
A | C | 1 | a0003c0009t0004g0428 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214+2925A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803396 | ||||||
| chr12:6803429
|
G | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0039 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214+2958G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803429 | ||||||
| chr12:6803507
|
G | A | 4 | a0002c0003t0007g0027a0002c0003t0007g0267a0002c0003t0007g0417others(1): Show | 4 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3036G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803507 | ||||||
| chr12:6803601
|
G | A | 304 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(301): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.214+3130G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803601 | ||||||
| chr12:6803611
|
C | G | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+3140C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803611 | ||||||
| chr12:6803647
|
T | G | 6 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(3): Show | 6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+3176T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803647 | ||||||
| chr12:6803676
|
C | T | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+3205C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803676 | ||||||
| chr12:6803740
|
G | A | 6 | a0001c0001t0001g0139a0001c0001t0004g0108a0001c0001t0004g0109others(3): Show | 6 | HG02132.hp2 NA18961.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+3269G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803740 | ||||||
| chr12:6803783
|
A | T | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+3312A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803783 | ||||||
| chr12:6803791
|
T | A | 3 | a0002c0003t0002g0011a0002c0003t0002g0012a0002c0003t0002g0032 | 3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.214+3320T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803791 | ||||||
| chr12:6803849
|
C | T | 2 | a0001c0002t0008g0273a0001c0002t0008g0275 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.214+3378C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803849 | ||||||
| chr12:6803858
|
T | A | 228 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.214+3387T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803858 | ||||||
| chr12:6803885
|
A | G | 353 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(350): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.214+3414A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803885 | ||||||
| chr12:6803965
|
T | G | 381 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(378): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.214+3494T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803965 | ||||||
| chr12:6804054
|
T | C | 1 | a0001c0010t0003g0422 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.214+3583T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804054 | ||||||
| chr12:6804067
|
C | T | 1 | a0001c0001t0001g0409 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.214+3596C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804067 | ||||||
| chr12:6804090
|
G | A | 7 | a0001c0004t0006g0074a0001c0004t0006g0116a0001c0004t0006g0148others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+3619G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804090 | ||||||
| chr12:6804111
|
A | AAAAT | 18 | a0001c0001t0004g0056a0001c0001t0004g0118a0001c0001t0004g0138others(15): Show | 19 | HG00738.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.214+3680_214+3683d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | |||||
| chr12:6804111
|
A | AAAATAAA others(1): Show |
8 | a0002c0003t0002g0011a0002c0003t0002g0012a0002c0003t0002g0032others(5): Show | 8 | HG01358.hp1 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+3676_214+3683d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | |||||
| chr12:6804111
|
AAAAT | A | 27 | a0001c0001t0001g0154a0001c0001t0001g0204a0001c0001t0001g0215others(24): Show | 27 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+3680_214+3683d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | |||||
| chr12:6804111
|
AAAATAAA others(1): Show |
A | 202 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.214+3676_214+3683d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | |||||
| chr12:6804111
|
AAAATAAA others(5): Show |
A | 110 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0155others(107): Show | 112 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.214+3672_214+3683d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | |||||
| chr12:6804127
|
T | C | 4 | a0002c0003t0002g0266a0002c0003t0002g0269a0002c0003t0002g0270others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3656T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804127 | ||||||
| chr12:6804162
|
G | GCA | 9 | a0001c0001t0004g0387a0002c0003t0001g0416a0002c0003t0001g0420others(6): Show | 9 | HG02559.hp1 HG03486.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+3720_214+3721d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | |||||
| chr12:6804162
|
G | GCACA | 3 | a0002c0003t0002g0001a0002c0003t0002g0115a0002c0003t0002g0249 | 4 | NA18944.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+3718_214+3721d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | |||||
| chr12:6804162
|
GCA | G | 11 | a0001c0001t0001g0224a0001c0001t0001g0323a0001c0001t0004g0242others(8): Show | 11 | HG00673.hp1 HG01192.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+3720_214+3721d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | |||||
| chr12:6804162
|
GCACACAC others(1): Show |
G | 4 | a0002c0003t0002g0266a0002c0003t0002g0269a0002c0003t0002g0270others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3714_214+3721d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | |||||
| chr12:6804162
|
GCACACAC others(9): Show |
G | 350 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(347): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.214+3706_214+3721d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | |||||
| chr12:6804170
|
A | G | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+3699A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804170 | ||||||
| chr12:6804180
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.214+3709A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804180 | ||||||
| chr12:6804190
|
A | T | 220 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.214+3719A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804190 | ||||||
| chr12:6804207
|
C | T | 8 | a0001c0001t0001g0333a0001c0004t0006g0074a0001c0004t0006g0116others(5): Show | 8 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+3736C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804207 | ||||||
| chr12:6804307
|
A | G | 1 | a0011c0017t0001g0423 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.214+3836A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804307 | ||||||
| chr12:6804346
|
GA | G | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+3880delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804346 | |||||
| chr12:6804380
|
A | G | 348 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(345): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.214+3909A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804380 | ||||||
| chr12:6804437
|
A | G | 2 | a0001c0001t0001g0323a0002c0003t0018g0016 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214+3966A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804437 | ||||||
| chr12:6804524
|
A | G | 174 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.214+4053A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804524 | ||||||
| chr12:6804600
|
T | C | 1 | a0001c0002t0003g0272 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.214+4129T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804600 | ||||||
| chr12:6804665
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG01168.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.214+4194G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804665 | ||||||
| chr12:6804694
|
G | A | 1 | a0001c0002t0003g0415 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.214+4223G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804694 | ||||||
| chr12:6804734
|
T | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0175 | 2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.214+4263T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804734 | ||||||
| chr12:6804788
|
G | A | 2 | a0001c0001t0001g0043a0010c0015t0019g0255 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.214+4317G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804788 | ||||||
| chr12:6804792
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0009g0110others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+4321G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804792 | ||||||
| chr12:6804941
|
G | A | 1 | a0001c0002t0003g0411 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.214+4470G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804941 | ||||||
| chr12:6804948
|
G | A | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+4477G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804948 | ||||||
| chr12:6805015
|
C | CA | 22 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0001t0001g0316others(19): Show | 22 | HG00621.hp2 HG01192.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.214+4563dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | |||||
| chr12:6805015
|
C | CAA | 64 | a0001c0001t0001g0237a0001c0001t0001g0323a0001c0001t0002g0046others(61): Show | 69 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.214+4562_214+4563d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | |||||
| chr12:6805015
|
C | CAAA | 12 | a0001c0001t0001g0224a0001c0001t0004g0108a0001c0001t0004g0242others(9): Show | 12 | HG02055.hp1 HG02074.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+4561_214+4563d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | |||||
| chr12:6805015
|
CA | C | 117 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.214+4563delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | |||||
| chr12:6805015
|
CAA | C | 15 | a0001c0001t0001g0122a0001c0001t0004g0126a0001c0002t0003g0081others(12): Show | 15 | HG01928.hp2 HG01978.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+4562_214+4563d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | |||||
| chr12:6805105
|
GC | G | 432 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(429): Show | 439 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(436): Show |
intron_variant | MODIFIER | c.214+4637delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805105 | |||||
| chr12:6805166
|
G | C | 350 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(347): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.214+4695G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805166 | ||||||
| chr12:6805184
|
C | CA | 11 | a0001c0001t0001g0224a0001c0001t0002g0046a0001c0001t0002g0311others(8): Show | 13 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+4735dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805184 | |||||
| chr12:6805198
|
AAAAAAAA others(2): Show |
A | 47 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0040others(44): Show | 47 | HG00741.hp1 HG01069.hp2 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+4732_214+4740d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805198 | |||||
| chr12:6805199
|
AAAAAAAA others(1): Show |
A | 157 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.214+4733_214+4740d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805199 | |||||
| chr12:6805200
|
AAAAAAAG | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0001t0001g0268others(12): Show | 15 | HG00099.hp1 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+4734_214+4740d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805200 | |||||
| chr12:6805202
|
AAAAAG | A | 10 | a0001c0001t0002g0053a0001c0001t0002g0120a0001c0001t0002g0392others(7): Show | 10 | HG02027.hp1 HG02040.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+4756_214+4760d others(7): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805202 | |||||
| chr12:6805203
|
AAAAG | A | 124 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0155others(121): Show | 127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.214+4736_214+4739d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805203 | |||||
| chr12:6805204
|
AAAG | A | 20 | a0001c0001t0002g0038a0001c0001t0002g0063a0001c0001t0002g0067others(17): Show | 20 | HG01358.hp1 HG02055.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+4736_214+4738d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805204 | |||||
| chr12:6805206
|
AG | A | 7 | a0001c0004t0006g0074a0001c0004t0006g0116a0001c0004t0006g0148others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+4736delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805206 | ||||||
| chr12:6805256
|
G | T | 1 | a0001c0001t0004g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+4785G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805256 | ||||||
| chr12:6805285
|
A | G | 19 | a0001c0001t0004g0126a0001c0002t0003g0081a0001c0002t0003g0092others(16): Show | 19 | HG00673.hp2 HG01928.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.214+4814A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805285 | ||||||
| chr12:6805293
|
T | A | 1 | a0001c0001t0001g0378 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.214+4822T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805293 | ||||||
| chr12:6805368
|
G | A | 1 | a0001c0001t0010g0168 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.214+4897G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805368 | ||||||
| chr12:6805518
|
T | G | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+5047T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805518 | ||||||
| chr12:6805559
|
TC | T | 6 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0404others(3): Show | 6 | HG01070.hp1 HG02897.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+5091delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805559 | |||||
| chr12:6805560
|
C | CA | 89 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0333others(86): Show | 93 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.214+5089_214+5090i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805560 | ||||||
| chr12:6805560
|
C | CAA | 8 | a0002c0003t0002g0001a0002c0003t0002g0079a0002c0003t0002g0112others(5): Show | 9 | HG03704.hp1 NA18944.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+5089_214+5090i others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805560 | ||||||
| chr12:6805561
|
C | A | 428 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(425): Show | 435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
intron_variant | MODIFIER | c.214+5090C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805561 | ||||||
| chr12:6805562
|
C | A | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+5091C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805562 | ||||||
| chr12:6805563
|
G | A | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+5092G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805563 | ||||||
| chr12:6805577
|
G | A | 1 | a0001c0001t0004g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.214+5106G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805577 | ||||||
| chr12:6805578
|
A | G | 1 | a0001c0001t0004g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.214+5107A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805578 | ||||||
| chr12:6805816
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.214+5345C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805816 | ||||||
| chr12:6805828
|
G | A | 1 | a0001c0002t0003g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.214+5357G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805828 | ||||||
| chr12:6805945
|
C | A | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0013others(2): Show | 7 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5474C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805945 | ||||||
| chr12:6805994
|
T | A | 88 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(85): Show | 93 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.214+5523T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805994 | ||||||
| chr12:6805996
|
C | T | 2 | a0001c0001t0001g0323a0002c0003t0018g0016 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214+5525C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805996 | ||||||
| chr12:6806037
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.214+5566C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806037 | ||||||
| chr12:6806072
|
G | C | 85 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(82): Show | 90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.214+5601G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806072 | ||||||
| chr12:6806136
|
C | CA | 118 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0154others(115): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.214+5678dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806136 | |||||
| chr12:6806149
|
AG | A | 8 | a0001c0001t0001g0333a0001c0004t0006g0074a0001c0004t0006g0116others(5): Show | 8 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+5680delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806149 | |||||
| chr12:6806150
|
G | A | 425 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(422): Show | 432 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(429): Show |
intron_variant | MODIFIER | c.214+5679G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806150 | ||||||
| chr12:6806154
|
C | A | 1 | a0001c0001t0004g0138 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.214+5683C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806154 | ||||||
| chr12:6806155
|
A | G | 1 | a0001c0001t0004g0138 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.214+5684A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806155 | ||||||
| chr12:6806156
|
T | TAC | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0087others(14): Show | 17 | HG01261.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+5711_214+5712d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | |||||
| chr12:6806156
|
TAC | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0265a0001c0001t0001g0305others(2): Show | 5 | HG02056.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+5711_214+5712d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | |||||
| chr12:6806156
|
TACAC | T | 83 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(80): Show | 88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.214+5709_214+5712d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | |||||
| chr12:6806156
|
TACACACA others(5): Show |
T | 1 | a0001c0018t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.214+5701_214+5712d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | |||||
| chr12:6806160
|
C | T | 1 | a0001c0001t0004g0138 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.214+5689C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806160 | ||||||
| chr12:6806176
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0004g0426 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.214+5707_214+5722d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806176 | |||||
| chr12:6806178
|
CACACATA others(7): Show |
C | 96 | a0001c0001t0001g0023a0001c0001t0001g0155a0001c0001t0002g0004others(93): Show | 98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.214+5709_214+5722d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806178 | |||||
| chr12:6806180
|
CACATACA others(5): Show |
C | 18 | a0001c0001t0002g0220a0001c0001t0002g0274a0001c0001t0002g0277others(15): Show | 18 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+5711_214+5722d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806180 | |||||
| chr12:6806182
|
C | CAT | 8 | a0001c0001t0001g0333a0001c0004t0006g0074a0001c0004t0006g0116others(5): Show | 8 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+5713_214+5714d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806182 | |||||
| chr12:6806182
|
C | T | 85 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(82): Show | 90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.214+5711C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806182 | ||||||
| chr12:6806182
|
CATACACA others(3): Show |
C | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+5715_214+5724d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806182 | |||||
| chr12:6806184
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.214+5713T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806184 | ||||||
| chr12:6806191
|
G | A | 318 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(315): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214+5720G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806191 | ||||||
| chr12:6806202
|
T | A | 116 | a0001c0001t0001g0023a0001c0001t0001g0155a0001c0001t0002g0004others(113): Show | 118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.214+5731T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806202 | ||||||
| chr12:6806242
|
T | C | 6 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(3): Show | 6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+5771T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806242 | ||||||
| chr12:6806269
|
C | T | 26 | a0001c0001t0001g0323a0002c0003t0001g0174a0002c0003t0001g0253others(23): Show | 27 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+5798C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806269 | ||||||
| chr12:6806286
|
A | C | 87 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(84): Show | 92 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.214+5815A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806286 | ||||||
| chr12:6806345
|
CCCAGGCT others(1): Show |
C | 57 | a0001c0001t0002g0004a0001c0001t0002g0038a0001c0001t0002g0053others(54): Show | 58 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.214+5875_214+5882d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806345 | ||||||
| chr12:6806353
|
G | A | 1 | a0002c0003t0007g0027 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.214+5882G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806353 | ||||||
| chr12:6806420
|
G | T | 4 | a0002c0003t0002g0266a0002c0003t0002g0269a0002c0003t0002g0270others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+5949G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806420 | ||||||
| chr12:6806740
|
G | A | 107 | a0001c0001t0001g0155a0001c0001t0002g0004a0001c0001t0002g0005others(104): Show | 109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.214+6269G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806740 | ||||||
| chr12:6806797
|
T | C | 28 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0102others(25): Show | 28 | HG00741.hp1 HG01069.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+6326T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806797 | ||||||
| chr12:6806820
|
G | A | 6 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(3): Show | 6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+6349G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806820 | ||||||
| chr12:6806893
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0013g0372 | 2 | NA18997.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.214+6422C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806893 | ||||||
| chr12:6806949
|
C | T | 1 | a0001c0001t0002g0385 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.214+6478C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806949 | ||||||
| chr12:6806994
|
T | C | 86 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(83): Show | 91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.214+6523T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806994 | ||||||
| chr12:6807023
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+6552C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807023 | ||||||
| chr12:6807083
|
T | C | 26 | a0001c0001t0001g0323a0002c0003t0001g0174a0002c0003t0001g0253others(23): Show | 27 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+6612T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807083 | ||||||
| chr12:6807099
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.214+6628G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807099 | ||||||
| chr12:6807113
|
G | A | 54 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0002g0088others(51): Show | 58 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.214+6642G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807113 | ||||||
| chr12:6807128
|
T | C | 92 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(89): Show | 97 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.214+6657T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807128 | ||||||
| chr12:6807148
|
C | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0040a0001c0001t0001g0262others(4): Show | 7 | HG01261.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+6677C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807148 | ||||||
| chr12:6807149
|
G | C | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+6678G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807149 | ||||||
| chr12:6807174
|
CAA | C | 84 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(81): Show | 89 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.214+6707_214+6708d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6807174 | |||||
| chr12:6807188
|
C | CA | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.214+6723dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6807188 | |||||
| chr12:6807344
|
G | A | 1 | a0001c0010t0003g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-6798G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807344 | ||||||
| chr12:6807345
|
T | G | 92 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(89): Show | 97 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.215-6797T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807345 | ||||||
| chr12:6807412
|
C | A | 1 | a0002c0003t0002g0424 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-6730C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807412 | ||||||
| chr12:6807419
|
G | C | 2 | a0001c0002t0008g0273a0001c0002t0008g0275 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.215-6723G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807419 | ||||||
| chr12:6807615
|
C | T | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-6527C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807615 | ||||||
| chr12:6807725
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.215-6417T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807725 | ||||||
| chr12:6807851
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.215-6291C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807851 | ||||||
| chr12:6807887
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0040 | 2 | HG01261.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.215-6255C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807887 | ||||||
| chr12:6807936
|
T | C | 1 | a0001c0001t0001g0386 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.215-6206T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807936 | ||||||
| chr12:6807940
|
C | T | 1 | a0001c0010t0003g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-6202C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807940 | ||||||
| chr12:6807973
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0039 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-6169G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807973 | ||||||
| chr12:6808052
|
C | T | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA19003.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.215-6090C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808052 | ||||||
| chr12:6808076
|
T | A | 92 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(89): Show | 97 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.215-6066T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808076 | ||||||
| chr12:6808079
|
C | CA | 27 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0154others(24): Show | 27 | HG00423.hp2 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.215-6039dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | |||||
| chr12:6808079
|
CA | C | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(152): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.215-6039delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | |||||
| chr12:6808079
|
CAA | C | 12 | a0001c0001t0001g0087a0001c0001t0001g0210a0001c0001t0001g0224others(9): Show | 13 | HG01884.hp2 HG01943.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-6040_215-6039d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | |||||
| chr12:6808079
|
CAAA | C | 74 | a0001c0001t0001g0237a0001c0001t0002g0088a0001c0001t0002g0101others(71): Show | 78 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.215-6041_215-6039d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | |||||
| chr12:6808079
|
CAAAA | C | 20 | a0001c0001t0001g0323a0002c0003t0001g0253a0002c0003t0001g0416others(17): Show | 20 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-6042_215-6039d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | |||||
| chr12:6808167
|
A | C | 2 | a0001c0001t0009g0110a0006c0013t0009g0158 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215-5975A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808167 | ||||||
| chr12:6808192
|
CGCCTGTA others(7): Show |
C | 7 | a0001c0001t0001g0155a0001c0001t0001g0319a0001c0001t0001g0328others(4): Show | 7 | HG01257.hp1 HG01358.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-5949_215-5936d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808192 | ||||||
| chr12:6808193
|
G | T | 5 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145others(2): Show | 5 | HG01192.hp1 HG02735.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-5949G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808193 | ||||||
| chr12:6808253
|
G | GA | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.215-5889_215-5888i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808253 | ||||||
| chr12:6808270
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0252 | 2 | NA18945.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.215-5872A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808270 | ||||||
| chr12:6808318
|
G | A | 156 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(153): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.215-5824G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808318 | ||||||
| chr12:6808324
|
C | T | 84 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(81): Show | 89 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.215-5818C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808324 | ||||||
| chr12:6808369
|
T | C | 5 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0013others(2): Show | 7 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-5773T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808369 | ||||||
| chr12:6808386
|
A | AG | 94 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(91): Show | 99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-5755dupG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808386 | |||||
| chr12:6808387
|
G | GC | 340 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(337): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.215-5755_215-5754i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808387 | ||||||
| chr12:6808445
|
T | C | 1 | a0001c0018t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.215-5697T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808445 | ||||||
| chr12:6808450
|
C | CA | 59 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0048others(56): Show | 59 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.215-5660dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAA | 23 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0035others(20): Show | 23 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.215-5661_215-5660d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAA | 7 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0002t0003g0132others(4): Show | 7 | HG01361.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-5662_215-5660d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAA | 6 | a0001c0001t0002g0096a0001c0001t0002g0286a0001c0001t0002g0288others(3): Show | 6 | HG00140.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-5664_215-5660d others(7): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAA | 33 | a0001c0001t0002g0060a0001c0001t0002g0066a0001c0001t0002g0068others(30): Show | 33 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.215-5665_215-5660d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA | 29 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0046others(26): Show | 31 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.215-5666_215-5660d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0002g0061a0001c0001t0002g0064a0001c0001t0002g0094others(6): Show | 9 | HG01169.hp1 HG02257.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.215-5667_215-5660d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(3): Show |
4 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-5669_215-5660d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(4): Show |
1 | a0006c0013t0009g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.215-5670_215-5660d others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0009g0110a0001c0004t0006g0074a0001c0004t0006g0179others(2): Show | 5 | HG00597.hp1 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-5671_215-5660d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(6): Show |
1 | a0002c0003t0005g0306 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.215-5672_215-5660d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(9): Show |
2 | a0001c0004t0006g0116a0001c0004t0006g0148 | 2 | HG03654.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.215-5675_215-5660d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(10): Show |
1 | a0001c0004t0006g0393 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.215-5676_215-5660d others(19): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
C | CAAAAAAA others(11): Show |
1 | a0001c0004t0006g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.215-5677_215-5660d others(20): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CA | C | 32 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 32 | HG01069.hp2 HG01255.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.215-5660delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAA | C | 14 | a0001c0001t0002g0038a0001c0001t0002g0053a0001c0001t0002g0072others(11): Show | 14 | HG00558.hp1 HG01109.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.215-5665_215-5660d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0324a0001c0001t0002g0296a0001c0001t0002g0297 | 3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.215-5670_215-5660d others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0268a0001c0001t0003g0018a0001c0001t0003g0039 | 3 | HG02572.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.215-5671_215-5660d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0001g0040a0001c0010t0003g0257 | 3 | HG01261.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.215-5672_215-5660d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAAA others(10): Show |
C | 2 | a0002c0003t0007g0427a0007c0020t0004g0322 | 2 | HG01358.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.215-5676_215-5660d others(19): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAAA others(11): Show |
C | 88 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(85): Show | 93 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.215-5677_215-5660d others(20): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808450
|
CAAAAAAA others(12): Show |
C | 4 | a0002c0003t0002g0266a0002c0003t0002g0269a0002c0003t0002g0270others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-5678_215-5660d others(21): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | |||||
| chr12:6808489
|
T | A | 94 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0323others(91): Show | 99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-5653T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808489 | ||||||
| chr12:6808502
|
T | A | 2 | a0001c0004t0006g0074a0001c0004t0006g0116 | 2 | HG00597.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.215-5640T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808502 | ||||||
| chr12:6808503
|
T | A | 30 | a0001c0001t0001g0323a0001c0004t0006g0074a0001c0004t0006g0116others(27): Show | 31 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.215-5639T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808503 | ||||||
| chr12:6808666
|
G | A | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(148): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.215-5476G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808666 | ||||||
| chr12:6808801
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-5341T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808801 | ||||||
| chr12:6808900
|
G | T | 2 | a0003c0009t0004g0028a0003c0009t0004g0428 | 2 | HG00738.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.215-5242G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808900 | ||||||
| chr12:6808955
|
C | T | 6 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-5187C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808955 | ||||||
| chr12:6809030
|
A | G | 94 | a0001c0001t0001g0224a0001c0001t0002g0046a0001c0001t0002g0088others(91): Show | 99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-5112A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809030 | ||||||
| chr12:6809269
|
C | A | 1 | a0002c0003t0007g0427 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.215-4873C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809269 | ||||||
| chr12:6809294
|
G | A | 7 | a0001c0004t0006g0074a0001c0004t0006g0116a0001c0004t0006g0148others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-4848G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809294 | ||||||
| chr12:6809358
|
T | C | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-4784T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809358 | ||||||
| chr12:6809373
|
G | A | 6 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4769G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809373 | ||||||
| chr12:6809444
|
C | A | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.215-4698C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809444 | ||||||
| chr12:6809449
|
T | C | 1 | a0002c0003t0007g0427 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.215-4693T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809449 | ||||||
| chr12:6809495
|
C | CA | 6 | a0001c0001t0001g0319a0001c0001t0002g0067a0001c0001t0004g0271others(3): Show | 6 | HG02293.hp2 HG02735.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4634dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809495 | |||||
| chr12:6809495
|
CA | C | 41 | a0001c0002t0003g0150a0001c0004t0006g0230a0001c0004t0006g0393others(38): Show | 42 | HG00408.hp1 HG00609.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.215-4634delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809495 | |||||
| chr12:6809646
|
T | C | 7 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(4): Show | 7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-4496T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809646 | ||||||
| chr12:6809666
|
C | T | 6 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4476C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809666 | ||||||
| chr12:6809752
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0071 | 2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.215-4390G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809752 | ||||||
| chr12:6809890
|
C | CT | 34 | a0001c0001t0002g0175a0001c0004t0006g0074a0001c0004t0006g0116others(31): Show | 35 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.215-4235dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809890 | |||||
| chr12:6809890
|
C | CTT | 158 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(155): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.215-4236_215-4235d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809890 | |||||
| chr12:6809890
|
C | CTTT | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.215-4237_215-4235d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809890 | |||||
| chr12:6809916
|
GTC | G | 94 | a0001c0001t0001g0224a0001c0001t0002g0046a0001c0001t0002g0088others(91): Show | 99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-4215_215-4214d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809916 | |||||
| chr12:6810034
|
C | T | 4 | a0001c0002t0003g0036a0001c0002t0003g0037a0001c0002t0003g0166others(1): Show | 4 | HG03017.hp1 HG03239.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-4108C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810034 | ||||||
| chr12:6810142
|
G | A | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-4000G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810142 | ||||||
| chr12:6810153
|
G | C | 85 | a0001c0001t0001g0224a0001c0001t0001g0323a0001c0001t0001g0413others(82): Show | 90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-3989G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810153 | ||||||
| chr12:6810185
|
T | TG | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.215-3956dupG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6810185 | |||||
| chr12:6810239
|
A | G | 1 | a0003c0009t0004g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-3903A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810239 | ||||||
| chr12:6810255
|
C | T | 1 | a0001c0018t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.215-3887C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810255 | ||||||
| chr12:6810403
|
A | G | 94 | a0001c0001t0001g0224a0001c0001t0001g0413a0001c0001t0002g0046others(91): Show | 99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-3739A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810403 | ||||||
| chr12:6810510
|
G | T | 1 | a0001c0001t0012g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215-3632G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810510 | ||||||
| chr12:6810589
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0039 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-3553A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810589 | ||||||
| chr12:6810592
|
C | A | 1 | a0001c0001t0001g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.215-3550C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810592 | ||||||
| chr12:6810685
|
C | T | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-3457C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810685 | ||||||
| chr12:6811099
|
A | G | 6 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-3043A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811099 | ||||||
| chr12:6811106
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.215-3036C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811106 | ||||||
| chr12:6811468
|
CTTTTCTT | C | 5 | a0001c0001t0002g0057a0001c0001t0002g0085a0001c0001t0002g0089others(2): Show | 5 | HG00621.hp1 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-2664_215-2658d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811468 | |||||
| chr12:6811472
|
T | C | 1 | a0003c0005t0004g0433 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.215-2670T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811472 | ||||||
| chr12:6811477
|
TTTCTTTT others(7): Show |
T | 6 | a0002c0003t0002g0078a0002c0003t0002g0079a0002c0003t0002g0112others(3): Show | 6 | NA18952.hp1 NA18956.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-2662_215-2649d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811477 | |||||
| chr12:6811478
|
TTCTTTTC others(6): Show |
T | 7 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0434others(4): Show | 7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-2662_215-2650d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811478 | |||||
| chr12:6811491
|
C | CT | 20 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0067others(17): Show | 20 | HG00408.hp1 HG00609.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-2632dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811491 | |||||
| chr12:6811491
|
CT | C | 141 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(138): Show | 141 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.215-2632delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811491 | |||||
| chr12:6811491
|
CTT | C | 75 | a0001c0001t0001g0048a0001c0001t0001g0413a0001c0001t0002g0088others(72): Show | 80 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.215-2633_215-2632d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811491 | |||||
| chr12:6811492
|
T | C | 7 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0434others(4): Show | 7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-2650T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811492 | ||||||
| chr12:6811493
|
T | C | 7 | a0002c0003t0002g0078a0002c0003t0002g0079a0002c0003t0002g0112others(4): Show | 7 | HG01891.hp1 NA18952.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-2649T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811493 | ||||||
| chr12:6811495
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.215-2647T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811495 | ||||||
| chr12:6811553
|
C | T | 1 | a0001c0001t0004g0007 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.215-2589C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811553 | ||||||
| chr12:6811671
|
C | CT | 104 | a0001c0001t0002g0038a0001c0001t0002g0053a0001c0001t0002g0057others(101): Show | 109 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.215-2460dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811671 | |||||
| chr12:6811791
|
G | A | 85 | a0001c0001t0002g0088a0001c0001t0002g0101a0001c0001t0002g0103others(82): Show | 90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-2351G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811791 | ||||||
| chr12:6811807
|
G | A | 6 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(3): Show | 6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-2335G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811807 | ||||||
| chr12:6811925
|
T | A | 1 | a0001c0001t0004g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.215-2217T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811925 | ||||||
| chr12:6811985
|
A | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0046a0001c0001t0002g0134others(6): Show | 10 | NA18942.hp1 NA18948.hp1 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-2157A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811985 | ||||||
| chr12:6812074
|
C | T | 1 | a0001c0001t0004g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-2068C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812074 | ||||||
| chr12:6812078
|
T | G | 86 | a0001c0001t0002g0088a0001c0001t0002g0101a0001c0001t0002g0103others(83): Show | 91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.215-2064T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812078 | ||||||
| chr12:6812129
|
G | A | 1 | a0001c0001t0004g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.215-2013G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812129 | ||||||
| chr12:6812140
|
C | G | 1 | a0002c0003t0018g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-2002C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812140 | ||||||
| chr12:6812229
|
T | C | 86 | a0001c0001t0002g0088a0001c0001t0002g0101a0001c0001t0002g0103others(83): Show | 91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.215-1913T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812229 | ||||||
| chr12:6812263
|
G | A | 1 | a0001c0001t0004g0010 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.215-1879G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812263 | ||||||
| chr12:6812548
|
G | A | 4 | a0001c0002t0003g0222a0001c0002t0003g0225a0001c0002t0003g0233others(1): Show | 4 | NA18970.hp2 NA19010.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1594G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812548 | ||||||
| chr12:6812619
|
C | T | 2 | a0001c0004t0006g0074a0001c0004t0006g0116 | 2 | HG00597.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.215-1523C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812619 | ||||||
| chr12:6812620
|
G | A | 5 | a0002c0003t0002g0266a0002c0003t0002g0269a0002c0003t0002g0270others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-1522G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812620 | ||||||
| chr12:6812660
|
C | T | 1 | a0001c0002t0003g0272 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.215-1482C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812660 | ||||||
| chr12:6812679
|
C | CA | 7 | a0001c0001t0001g0102a0001c0001t0004g0403a0002c0003t0002g0266others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1451dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812679 | |||||
| chr12:6812767
|
ATT | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0002c0003t0001g0253others(16): Show | 19 | HG01358.hp1 HG01993.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.215-1371_215-1370d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | |||||
| chr12:6812767
|
ATTTT | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0215a0001c0001t0001g0324others(7): Show | 10 | HG00642.hp2 HG03130.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1373_215-1370d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | |||||
| chr12:6812767
|
ATTTTTG | A | 122 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.215-1373_215-1368d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | |||||
| chr12:6812767
|
ATTTTTGT others(1): Show |
A | 6 | a0002c0003t0005g0026a0002c0003t0005g0029a0002c0003t0005g0030others(3): Show | 6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1373_215-1366d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | |||||
| chr12:6812767
|
ATTTTTGT others(3): Show |
A | 2 | a0001c0001t0001g0127a0001c0001t0002g0282 | 2 | HG01175.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.215-1373_215-1364d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | |||||
| chr12:6812767
|
ATTTTTGT others(5): Show |
A | 102 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0038others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.215-1373_215-1362d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | |||||
| chr12:6812769
|
T | G | 1 | a0009c0016t0001g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.215-1373T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812769 | ||||||
| chr12:6812769
|
T | TTG | 9 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0013others(6): Show | 13 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-1372_215-1371i others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812769
|
T | TTGTG | 27 | a0001c0001t0004g0056a0001c0001t0004g0109a0001c0001t0004g0138others(24): Show | 27 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.215-1372_215-1371i others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812769
|
T | TTGTGTG | 3 | a0001c0001t0004g0034a0001c0001t0004g0108a0001c0001t0004g0123 | 3 | HG03453.hp2 HG03669.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.215-1372_215-1371i others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812769
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0004g0118a0001c0001t0009g0110a0006c0013t0009g0158 | 3 | HG02129.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215-1372_215-1371i others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812769
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0004g0062a0001c0001t0004g0126 | 2 | NA18995.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.215-1372_215-1371i others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812769
|
TTTTG | T | 7 | a0001c0004t0006g0074a0001c0004t0006g0116a0001c0004t0006g0148others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1371_215-1368d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812769
|
TTTTGTG | T | 7 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(4): Show | 7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-1371_215-1366d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | |||||
| chr12:6812771
|
T | G | 74 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0103others(71): Show | 79 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.215-1371T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812771 | ||||||
| chr12:6812771
|
T | TTG | 11 | a0001c0001t0001g0342a0001c0001t0002g0069a0001c0001t0002g0090others(8): Show | 11 | HG00438.hp1 HG00597.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-1335_215-1334d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812771 | |||||
| chr12:6812771
|
T | TTGTG | 5 | a0001c0001t0003g0039a0001c0002t0003g0081a0001c0002t0003g0092others(2): Show | 5 | HG02080.hp2 HG02735.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1337_215-1334d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812771 | |||||
| chr12:6812773
|
G | T | 2 | a0001c0002t0003g0193a0001c0002t0003g0198 | 2 | HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.215-1369G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812773 | ||||||
| chr12:6812891
|
A | AT | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.215-1250dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812891 | |||||
| chr12:6812912
|
GT | G | 4 | a0001c0001t0009g0110a0001c0018t0002g0156a0005c0008t0004g0006others(1): Show | 5 | HG02970.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1221delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812912 | |||||
| chr12:6812947
|
G | A | 3 | a0001c0001t0009g0110a0001c0018t0002g0156a0006c0013t0009g0158 | 3 | HG02970.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.215-1195G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812947 | ||||||
| chr12:6812974
|
C | G | 1 | a0009c0016t0001g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.215-1168C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812974 | ||||||
| chr12:6813008
|
G | A | 1 | a0001c0001t0004g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.215-1134G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813008 | ||||||
| chr12:6813082
|
C | T | 1 | a0001c0001t0001g0401 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.215-1060C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813082 | ||||||
| chr12:6813083
|
T | C | 1 | a0001c0001t0001g0401 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.215-1059T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813083 | ||||||
| chr12:6813219
|
A | T | 2 | a0001c0002t0003g0391a0001c0002t0003g0402 | 2 | NA18980.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.215-923A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813219 | ||||||
| chr12:6813220
|
A | AT | 78 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0047others(75): Show | 78 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.215-903dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6813220 | |||||
| chr12:6813220
|
A | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0002t0003g0295others(1): Show | 4 | HG00639.hp2 HG01109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-922A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813220 | ||||||
| chr12:6813220
|
AT | A | 86 | a0001c0001t0002g0103a0001c0001t0002g0175a0001c0001t0002g0314others(83): Show | 90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-903delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6813220 | |||||
| chr12:6813220
|
ATTT | A | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-905_215-903del others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6813220 | |||||
| chr12:6813222
|
T | A | 2 | a0002c0003t0002g0424a0008c0014t0016g0264 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-920T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813222 | ||||||
| chr12:6813223
|
T | A | 1 | a0001c0001t0001g0377 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215-919T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813223 | ||||||
| chr12:6813224
|
T | A | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-918T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813224 | ||||||
| chr12:6813328
|
A | T | 103 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0038others(100): Show | 105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.215-814A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813328 | ||||||
| chr12:6813466
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.215-676A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813466 | ||||||
| chr12:6813536
|
G | T | 351 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(348): Show | 358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.215-606G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813536 | ||||||
| chr12:6813841
|
A | G | 1 | a0001c0001t0001g0377 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215-301A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813841 | ||||||
| chr12:6813852
|
G | A | 153 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(150): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.215-290G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813852 | ||||||
| chr12:6813935
|
T | A | 83 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(80): Show | 88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.215-207T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813935 | ||||||
| chr12:6814054
|
A | G | 1 | a0001c0001t0004g0387 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.215-88A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814054 | ||||||
| chr12:6814068
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.215-74G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814068 | ||||||
| chr12:6814120
|
C | G | 83 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(80): Show | 88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.215-22C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814120 | ||||||
| chr12:6814122
|
C | T | 2 | a0001c0001t0002g0312a0001c0001t0002g0313 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.215-20C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814122 | ||||||
| chr12:6814305
|
G | A | 1 | a0001c0001t0002g0190 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.373+5G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814305 | ||||||
| chr12:6814365
|
C | T | 2 | a0001c0001t0004g0394a0005c0008t0004g0006 | 3 | NA18974.hp2 NA19056.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.373+65C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814365 | ||||||
| chr12:6814370
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.373+70C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814370 | ||||||
| chr12:6814549
|
A | G | 1 | a0001c0001t0004g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.374-210A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814549 | ||||||
| chr12:6814665
|
C | T | 86 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(83): Show | 91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.374-94C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814665 | ||||||
| chr12:6815131
|
C | T | 246 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.607+139C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815131 | ||||||
| chr12:6815154
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.607+162G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815154 | ||||||
| chr12:6815168
|
G | A | 1 | a0001c0018t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.607+176G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815168 | ||||||
| chr12:6815179
|
G | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.607+187G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815179 | ||||||
| chr12:6815241
|
G | A | 1 | a0001c0002t0003g0292 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.607+249G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815241 | ||||||
| chr12:6815320
|
C | T | 1 | a0001c0002t0003g0058 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.607+328C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815320 | ||||||
| chr12:6815349
|
G | A | 1 | a0008c0014t0016g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.607+357G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815349 | ||||||
| chr12:6815495
|
G | A | 8 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(5): Show | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+503G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815495 | ||||||
| chr12:6815516
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.607+524G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815516 | ||||||
| chr12:6815552
|
C | A | 246 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.608-504C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815552 | ||||||
| chr12:6815614
|
G | C | 1 | a0008c0014t0016g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.608-442G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815614 | ||||||
| chr12:6815661
|
C | T | 1 | a0001c0018t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.608-395C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815661 | ||||||
| chr12:6815691
|
G | A | 1 | a0002c0003t0002g0249 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.608-365G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815691 | ||||||
| chr12:6815827
|
T | A | 1 | a0007c0020t0004g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.608-229T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815827 | ||||||
| chr12:6815954
|
C | T | 1 | a0001c0001t0001g0381 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.608-102C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815954 | ||||||
| chr12:6815983
|
C | T | 103 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0038others(100): Show | 105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.608-73C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815983 | ||||||
| chr12:6816052
|
C | G | 1 | a0002c0003t0007g0427 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.608-4C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6816052 | ||||||
| chr12:6816660
|
C | T | 1 | a0001c0002t0003g0430 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+257C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/9 | chr12 | 6816660 | ||||||
| chr12:6816763
|
T | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.955+360T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/9 | chr12 | 6816763 | ||||||
| chr12:6816769
|
G | C | 1 | a0001c0001t0013g0372 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.956-361G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/9 | chr12 | 6816769 | ||||||
| chr12:6817505
|
A | G | 57 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(54): Show | 61 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1156+175A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817505 | ||||||
| chr12:6817610
|
G | GC | 17 | a0002c0003t0001g0174a0002c0003t0001g0253a0002c0003t0001g0416others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1156+286dupC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817610 | |||||
| chr12:6817649
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1156+319C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817649 | ||||||
| chr12:6817675
|
T | C | 2 | a0001c0001t0002g0088a0001c0001t0002g0101 | 2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1156+345T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817675 | ||||||
| chr12:6817691
|
T | C | 7 | a0001c0004t0006g0074a0001c0004t0006g0116a0001c0004t0006g0148others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156+361T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817691 | ||||||
| chr12:6817694
|
A | G | 1 | a0001c0001t0004g0406 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1156+364A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817694 | ||||||
| chr12:6817731
|
ACT | A | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(46): Show | 49 | HG00741.hp1 HG01069.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.1156+403_1156+404d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817731 | |||||
| chr12:6817743
|
G | A | 1 | a0011c0017t0001g0423 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1156+413G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817743 | ||||||
| chr12:6817753
|
ATACACAC others(2): Show |
A | 85 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(82): Show | 89 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1156+433_1156+441d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817753 | |||||
| chr12:6817767
|
C | T | 1 | a0001c0002t0003g0430 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1156+437C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817767 | ||||||
| chr12:6817778
|
ACT | A | 18 | a0002c0003t0001g0174a0002c0003t0001g0253a0002c0003t0001g0416others(15): Show | 18 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.1156+450_1156+451d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817778 | |||||
| chr12:6817796
|
AC | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1156+470delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817796 | |||||
| chr12:6817819
|
A | G | 111 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0038others(108): Show | 114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1156+489A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817819 | ||||||
| chr12:6817824
|
C | T | 1 | a0001c0010t0003g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1156+494C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817824 | ||||||
| chr12:6817828
|
C | T | 1 | a0001c0002t0003g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1156+498C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817828 | ||||||
| chr12:6817857
|
T | TCA | 84 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(81): Show | 88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1156+532_1156+533d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817857 | |||||
| chr12:6817869
|
GCA | G | 22 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0001t0001g0117others(19): Show | 22 | HG00621.hp2 HG01891.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.1157-542_1157-541d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817869 | |||||
| chr12:6817872
|
C | T | 8 | a0002c0003t0001g0174a0002c0003t0001g0253a0002c0003t0001g0416others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1156+542C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817872 | ||||||
| chr12:6817878
|
CACTT | C | 3 | a0001c0004t0006g0148a0001c0004t0006g0179a0001c0004t0006g0251 | 3 | HG03654.hp1 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1157-540_1157-537d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817878 | |||||
| chr12:6817879
|
A | ACT | 67 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(64): Show | 71 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1157-541_1157-540d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817879 | |||||
| chr12:6817879
|
A | T | 17 | a0002c0003t0001g0174a0002c0003t0001g0253a0002c0003t0001g0416others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1157-542A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817879 | ||||||
| chr12:6817887
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0214 | 2 | NA18939.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1157-534A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817887 | ||||||
| chr12:6817925
|
G | A | 1 | a0001c0002t0003g0171 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1157-496G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817925 | ||||||
| chr12:6817938
|
C | A | 18 | a0002c0003t0001g0174a0002c0003t0001g0253a0002c0003t0001g0416others(15): Show | 18 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.1157-483C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817938 | ||||||
| chr12:6817980
|
A | G | 17 | a0002c0003t0001g0174a0002c0003t0001g0253a0002c0003t0001g0416others(14): Show | 17 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1157-441A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817980 | ||||||
| chr12:6817989
|
C | T | 1 | a0001c0001t0001g0368 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1157-432C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817989 | ||||||
| chr12:6817990
|
G | A | 2 | a0001c0002t0003g0339a0001c0002t0003g0351 | 2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1157-431G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817990 | ||||||
| chr12:6817992
|
G | A | 353 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(350): Show | 360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1157-429G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817992 | ||||||
| chr12:6818000
|
A | C | 91 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(88): Show | 95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-421A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818000 | ||||||
| chr12:6818027
|
C | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0040a0001c0001t0001g0262others(1): Show | 4 | HG01261.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157-394C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818027 | ||||||
| chr12:6818068
|
A | G | 91 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(88): Show | 95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-353A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818068 | ||||||
| chr12:6818081
|
G | C | 91 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(88): Show | 95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-340G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818081 | ||||||
| chr12:6818088
|
ACGCGCAC others(3): Show |
A | 254 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1157-323_1157-314d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6818088 | |||||
| chr12:6818092
|
G | A | 91 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(88): Show | 95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-329G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818092 | ||||||
| chr12:6818092
|
G | GCA | 7 | a0001c0002t0003g0132a0001c0002t0003g0149a0001c0002t0003g0279others(4): Show | 7 | HG02451.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1157-325_1157-324d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6818092 | |||||
| chr12:6818101
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1157-320C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818101 | ||||||
| chr12:6818102
|
G | A | 20 | a0001c0002t0003g0347a0002c0003t0001g0174a0002c0003t0001g0253others(17): Show | 20 | HG00733.hp2 HG01358.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1157-319G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818102 | ||||||
| chr12:6818102
|
GCA | G | 3 | a0002c0003t0002g0011a0002c0003t0002g0012a0002c0003t0002g0032 | 3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1157-308_1157-307d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6818102 | |||||
| chr12:6818108
|
A | G | 88 | a0001c0001t0002g0103a0001c0001t0004g0002a0001c0001t0004g0003others(85): Show | 92 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.1157-313A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818108 | ||||||
| chr12:6818110
|
A | G | 3 | a0002c0003t0002g0011a0002c0003t0002g0012a0002c0003t0002g0032 | 3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1157-311A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818110 | ||||||
| chr12:6818119
|
C | T | 4 | a0001c0001t0003g0018a0001c0001t0003g0039a0001c0010t0003g0257others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157-302C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818119 | ||||||
| chr12:6818297
|
C | T | 1 | a0001c0002t0003g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1157-124C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818297 | ||||||
| chr12:6818304
|
C | T | 248 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1157-117C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818304 | ||||||
| chr12:6818374
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0019 | 2 | HG01109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1157-47G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818374 | ||||||
| chr12:6818618
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0039 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1278+76A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/9 | chr12 | 6818618 | ||||||
| chr12:6818651
|
G | A | 1 | a0001c0002t0003g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1278+109G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/9 | chr12 | 6818651 | ||||||
| chr12:6818762
|
C | T | 1 | a0010c0015t0019g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1279-85C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/9 | chr12 | 6818762 | ||||||
| chr12:6818933
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1346+19G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818933 | ||||||
| chr12:6818958
|
GGGGA | G | 6 | a0003c0005t0004g0431a0003c0005t0004g0432a0003c0005t0004g0433others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+50_1346+53del others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 6818958 | |||||
| chr12:6818964
|
G | T | 5 | a0001c0001t0009g0110a0002c0003t0002g0011a0002c0003t0002g0012others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346+50G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818964 | ||||||
| chr12:6818969
|
T | G | 434 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(431): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.1346+55T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818969 | ||||||
| chr12:6818970
|
A | G | 279 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1346+56A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818970 | ||||||
| chr12:6819048
|
C | T | 190 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0019others(187): Show | 194 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.1346+134C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6819048 |